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Introduction Meckel's diverticulum is a congenital anomaly that is often detected incidentally. When it presents symptomatically, it causes painless gastrointestinal bleeding. Nevertheless, in rare instances, it can cause acute intestinal obstruction, often obscuring the true clinical picture. Case presentation A 31-year-old male presented to the emergency department with a 24-hour history of unremitting nausea, biliary emesis, abdominal distension, and absolute constipation. After ruling out the most common etiologies of acute bowel obstruction, radiological imaging was obtained and was suggestive of meckel's diverticulum. Laparoscopic meckel's diverticulectomy was performed, with the subsequent histopathological analysis confirming ectopic gastric tissue. Discussion Meckel's diverticulum occurs consequent to incomplete obliteration of the vitelline or omphalomesenteric duct, which connects the developing intestines to the yolk sac. It is found in roughly 2% of the population, of which only about 4% may become symptomatic due to any number of complications. Specifically, small bowel obstruction (SBO) and diverticulitis secondary to ectopic gastric or pancreatic tissue are the most common presentations of symptomatic MD. Conclusion Although relatively rare in adults, MD should be considered in the list of differentials in patients with intussusception leading to SBO, especially on a background history unremarkable for the most common etiologies causing SBO including post-operative adhesions and hernias.
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CORRECTED PROOF
Annals of Medicine and Surgery xxx (xxxx) 103734
Contents lists available at ScienceDirect
Annals of Medicine and Surgery
journal homepage: www.elsevier.com/locate/amsu
Case Report
Meckel's diverticulum causing acute intestinal obstruction: A case report
and comprehensive review of the literature
Talal Almas a,, Abdulla K. Alsubai a, Danyal Ahmed a, Muneeb Ullah b, Muhammad Faisal Murad b,
Khadeer AbdulKarim a, Eissa Sultan Alwheibi a, Mohamed Alansaari a, Tala Abdull atif c,
Sebastian Hadeed a, Muhammad Omer Khan a, Majid Alsufyani a, Enaam Alzadjali a, Arjun Samy a,
Mert Oruk a, Mhmod Kadom a, Fatemah Saleh Alhajri a, Ahmed Barakat a,
Maen Monketh Alrawashdeh a, Mohammad Said a, Reem AlDhaheri a, Emad Mansoor d
aRoyal College of Surgeons in Ireland, Dublin, Ireland
bMaroof International Hospital, Islamabad, Pakistan
cNational University of Ireland Galway, Galway, Ireland
dDivision of Gastroenterology and Liver Disease, University Hospitals Cleveland Medical Center, Case Western Reserve University, Cleveland, OH, USA
ARTICLE INFO
Keywords:
Meckel's diverticulum
Acute intestinal obstruction
ABSTRACT
Introduction: Meckel's diverticulum is a congenital anomaly that is often detected incidentally. When it presents
symptomatically, it causes painless gastrointestinal bleeding. Nevertheless, in rare instances, it can cause acute
intestinal obstruction, often obscuring the true clinical picture.
Case presentation: A 31-year-old male presented to the emergency department with a 24-h history of unremitting
nausea, biliary emesis, abdominal distension, and absolute constipation. After ruling out the most common eti-
ologies of acute bowel obstruction, radiological imaging was obtained and was suggestive of meckel's diverticu-
lum. Laparoscopic meckel's diverticulectomy was performed, with the subsequent histopathological analysis
confirming ectopic gastric tissue.
Discussion: Meckel's diverticulum occurs consequent to incomplete obliteration of the vitelline or omphalome-
senteric duct, which connects the developing intestines to the yolk sac. It is found in roughly 2% of the popula-
tion, of which only about 4% may become symptomatic due to any number of complications. Specifically, small
bowel obstruction (SBO) and diverticulitis secondary to ectopic gastric or pancreatic tissue are the most common
presentations of symptomatic MD.
Conclusion: Although relatively rare in adults, MD should be considered in the list of differentials in patients
with intussusception leading to SBO, especially on a background history unremarkable for the most common
etiologies causing SBO including post-operative adhesions and hernias.
1. Introduction
Acute intestinal obstruction continues to be a medical and surgical
emergency that warrants an emergency intervention. Acute bowel ob-
struction usually presents with a vague constellation of symptoms, of-
ten characterized by bilious/non-bilious emesis, nausea, vomiting,
anorexia, and abdominal pain [1]. While postoperative adhesions and
tumors afflicting the bowel remain leading causes of acute intestinal ob-
struction, rarer entities, such as Meckel's diverticulum, can seldom be
the source, often obscuring the true clinical picture [2,3]. In gastroen-
terology literature, post-operative adhesions and hernias are frequently
cited as being the leading causes of small bowel obstruction. However,
rare congenital abnormalities such as meckel's diverticulum are not
routinely thought to be the source of acute small bowel obstruction
[2,3]. Meckel's diverticulum (MD) is defined as a congenital anomaly
that ensues in the wake of partial closure and persistence of the
vitelline, or the omphalomesenteric, duct during embryogenesis [1,2].
This usually occurs in the fifth week of development and causes a true
outpouching of the small intestine, located approximately two feet from
the ileocecal valve [2,3]. It is the most common congenital abnormality
afflicting the gastrointestinal tract and has been reported in up to 13%
of patients [2]. MD, a true diverticulum, involves all layers of the small
Corresponding author. Royal College of Surgeons in Ireland, 123 St. Stephen's Green, Dublin, Ireland.
E-mail address: Talalalmas.almas@gmail.com (T. Almas).
https://doi.org/10.1016/j.amsu.2022.103734
Received 16 March 2022; Received in revised form 1 May 2022; Accepted 4 May 2022
2049-0801/© 20XX
Note: Low-resolution images were used to create this PDF. The original images will be used in the final composition.
CORRECTED PROOF
T. Almas et al. Annals of Medicine and Surgery xxx (xxxx) 103734
Fig. 1. An abdominal x-ray divulging multiple air-fluid levels within the colon,
thus alluding to an obstructive etiology.
intestine and is known to contain ectopic gastric mucosa [1]. It is gener-
ally asymptomatic and is usually discovered incidentally during surgi-
cal exploration of other diseases or less commonly through diagnostic
imaging [1]. However, hemorrhagic, inflammatory, and obstructive
complications can arise [13]. Additionally, MD can present with pain-
less bleeding due to ectopic gastric acid and pepsin production in the di-
verticulum (gastric mucosa or pancreatic differentiation in MD mu-
cosa), further complicating the clinical picture [3,4]. In patients pre-
senting with painless gastrointestinal bleeding of unknown etiology,
MD may be suspected [2,3]. Nonetheless, acute intestinal obstruction
consequent to the presence of meckel's diverticulum in the adult popu-
lation remains a clinical enigma [3,4]. Herein, we elucidate the case of
a 31-year-old male who presented with chief complaints of nausea, bil-
iary emesis, and abdominal distension on a background of unremark-
able medical and surgical history. Further investigative workup di-
vulged the presence of meckel's diverticulum, with subsequent divertic-
ulectomy resulting in prompt abatement of the patient's symptoms. The
overarching objective of the present paper is to prompt clinicians to rec-
ognize MD as a potential cause of acute small bowel obstruction. Al-
though the patient's age at presentation can yield imperative diagnostic
cues, MD should nevertheless be considered in the list of differentials in
patients presenting with acute small bowel obstruction regardless of
age.
2. Case presentation
A 31-year-old male presented to the emergency department with a
24-h history of unremitting nausea, biliary emesis, abdominal disten-
sion, and absolute constipation. Notably, the patient's last regular
bowel movement had been three days prior to the current presentation,
with the patient erroneously attributing his altered bowel habits to his
recent onset of anorexia of unknown origin. The patient reported no red
flag symptoms, affirmatively denying recent fevers, previously altered
bowel habits, infectious urinary symptoms, or weight loss. The patient's
prior medical and surgical histories were unimpressive, and he reported
no other comorbidities. Pertinently, the patient had had an episode sim-
ilar to the current one four years ago; at the time, his condition was
managed conservatively and resulted in a prompt resolution of his
symptoms within 24 hours of his presentation to the hospital. The pa-
tient remained asymptomatic thereafter with no consequent episodes
till the current presentation.
Upon clinical examination, the patient appeared profusely unwell,
with excruciating, 7/10, vague, non-localized abdominal pain that
caused significant distress to the patient. Abdominal examination re-
vealed a soft, distended abdomen that was non-tender with no evidence
of rigidity, peritonitis, or guarding. Pertinently, bowel sounds were au-
dible and were noted to be tinkling in nature, raising the initial suspi-
cions for an obstructive etiology underlying the patient's clinical pre-
sentation. The murphy's sign, along with the psoas, obturator, and rovs-
ing's signs, were all negative and unimpressive, effectively ruling out
acute cholecystitis and acute appendicitis as plausible etiologies. The
patient's past surgical history was also unimpressive, further precluding
post-operative adhesions as the likely etiology. Upon clinical examina-
tion, there was no evidence of hernial protrusions, and the genital ori-
fices were unremarkable. Furthermore, clinical examination of the ab-
domen did not reveal any rigidity or guarding, and no signs of peritoni-
tis were appreciated. The patient's C-reactive protein was raised to 15;
however, his remaining labs were unremarkable for any pertinent de-
rangements. In order to better delineate the etiology underlying the pa-
tient's presentation, an abdominal x-ray was obtained and revealed
multiple air-fluid levels in the small bowel (Fig. 1).
Based on the patient's x-ray findings, an obstructive pathology was
deemed plausible. However, given that the patient demonstrated an un-
remarkable surgical history and did not show signs of a possible gas-
trointestinal malignancy, adhesions, and tumor as causes of acute in-
testinal obstruction were effectively ruled out. Further radiological in-
vestigation through the means of a computed tomography (CT) scan di-
Fig. 2. CT scan of the patient's abdomen showing a transition point in the terminal ileum (red arrow), with mesenteric band cut-off. (For interpretation of the refer-
ences to colour in this figure legend, the reader is referred to the Web version of this article.)
2
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T. Almas et al. Annals of Medicine and Surgery xxx (xxxx) 103734
Fig. 3. CT scan of the abdomen showing the presence of meckel's loops (red ar-
row), further alluding to the presence of meckel's diverticulum. (For interpreta-
tion of the references to colour in this figure legend, the reader is referred to the
Web version of this article.)
vulged a transition point in the terminal ileum, with mesenteric band
cut-off, strongly alluding to the presence of a diverticulum in the speci-
fied region (Fig. 2).
The CT imaging of the abdomen further revealed the presence of the
classical meckel's loops, thereby confirming the presence of meckel's di-
verticulum (Fig. 3).
Considering the impression obtained from the patient's radiological
work-up, a multidisciplinary team meeting (MDT) was conducted. The
presence of meckel's diverticulum due to an acute small bowel obstruc-
tion was deemed exceedingly plausible. Consequently, the patient was
managed using conservative measures for the next 24 hours; however,
the patient refused a nasogastric tube, which would have been pivotal
in relieving the obstruction. During this time, the patient had an
episode of nominal bowel motion once but did not pass any flatus. Con-
servative treatment was thus continued, and the patient was prepared
for a laparoscopic diverticulectomy.
During the operation, meckel's diverticulum in close proximity to
the ileocecal valve was confirmed. Per-operative evaluation divulged
meckel's diverticulitis with the tip attached to the ileal mesentery
through the means of a band (Fig. 4).
Given this intraoperative finding, tip and band release was per-
formed (Fig. 5).
Additionally, given the presence of meckel's diverticulitis and the
fact that the patient had been symptomatic four years prior to the cur-
rent episode, meckel's diverticulectomy was performed (Fig. 6).
The surgery was conducted unremarkably, with no intra- or periop-
erative complications encountered during the process. Postoperatively,
the patient remained well and symptom-free except for a minor wound
infectious from the hypogastric port used for specimen delivery during
the surgery. Daily wound dressings were advised without the need for
antibiotics.
The subsequent histopathology report confirmed the presence of dif-
fusely inflamed ectopic gastric mucosa in close proximity to the ileoce-
cal valve, reinforcing meckel's diverticulum as the culprit etiology un-
derlying the patient's episode.
The present paper was reported in line with the SCARE guidelines
[5].
3. Discussion
Meckel's diverticulum (MD) is one of several congenital abnormali-
ties that can result from incomplete obliteration of the vitelline or om-
phalomesenteric duct, which connects the developing intestines to the
yolk sac during development, and is a true diverticulum composed of
all intestinal layers [6]. It is found in roughly 2% of the population, of
which only about 4% may become symptomatic due to any number of
complications [6]. Specifically, small bowel obstruction (SBO) and di-
verticulitis secondary to ectopic gastric or pancreatic tissue are the
most common presentations of symptomatic MD [7]. When it does pre-
sent with obstructive symptoms, subsequent complications may arise in
up to 36.5% of cases via a vast myriad of mechanisms [8]. Obstruction
can commonly occur due to volvulus or torsion of the intestine around a
fibrous band from MD to the umbilicus; intussusception or inversion of
the MD into the ileum or cecum; or mesodiverticular band trapping the
small bowel under the vascular supply of the MD and potentially lead-
ing to strangulation [9]. With symptomatic MD patients representing
only 0.08% of the total population, the exceeding rarity of the condition
leads to poor rates of pre-operative diagnosis, thereby obscuring the
Fig. 4. Per-operative image delineating meckel's diverticulitis with the tip attached to the ileal mesentery through the means of a band.
3
CORRECTED PROOF
T. Almas et al. Annals of Medicine and Surgery xxx (xxxx) 103734
Fig. 5. Intraoperative image demonstrating tip and band release.
Fig. 6. Per-operative image obtained after meckel's diverticulectomy was performed.
true clinical picture [9]. Early recognition is of paramount importance
since a delay in surgery of 36 hours or more can triple the mortality rate
from 8% to 25% in patients presenting with strangulation [10]. In this
context, it is imperative that clinicians are aware of MD, its associated
clinical findings, and the best practices for its diagnosis and manage-
ment.
The present study elucidates a case of a 31-year-old male patient
with acute onset of symptoms consistent with obstruction. The patient
presented with the classical tetrad of bowel obstruction involving nau-
sea, emesis, abdominal distension, and constipation [11]. Diagnostic
imaging showed multiple air-fluid levels, which indicate pathological
accumulation of fluid and gas and are a hallmark finding in X-ray and
CT of SBO [12]. Ultrasound for Meckel's Diverticulum is feasible and
can identify mesodiverticular bands as a hyperechoic line, particularly
in pediatric patients. However, CT scan was found to be more accurate
in determining the cause of small bowel obstruction in adults [13]. In
cases with ectopic mucosa in the diverticular outpouch, a Meckel's ra-
dionuclide scan, which injects technetium-99 m as a dye to detect gas-
tric tissue, can be performed [14]. A previous study found the transition
zone was located near the midline in 80% of patients. In our case, the
transition point was identified in the terminal or distal ileum [15].
Interestingly, volvulus of the MD was not suspected as a mechanism
of obstruction in our case as there was no fibrous band connecting the
MD to the umbilicus. We also did not suspect intussusception of the
small bowel due to the absence of inversion of the diverticular out-
pouching into the ileum or cecum. The subsequent histopathology re-
port showed unremarkable intestinal tissue. The lack of ectopic tissue
thus suggests diverticulitis as a cause of inflammation, and subsequent
obstruction was not a likely differential. Instead, the tip of the Meckel's
diverticulum with a band attached to the ileal mesentery was discov-
ered per-operatively during the diverticulectomy. Thus, mesodiverticu-
lar band (MDB) of Meckel's diverticulum was determined to be the
cause of SBO in this patient. The MDB is a remnant of the vitelline
artery, which supplies Meckel's Diverticulum and provides a bridge for
bowel loops to herniate and become strangulated, gangrenous, is-
chemic, or otherwise mechanically obstructed [16,17].
Surgery, in specific meckel's diverticulectomy, remains the mainstay
of treatment in such cases. The most common forms are diverticulec-
tomy, wedge, or segmental resection, and the rationale for which proce-
dure to form depends largely on the integrity of the diverticular base
and proximal ileum and the location of ectopic tissue if any [3]. Wedge
or segmental resection is recommended for MD with SBO; however, di-
verticulectomy was performed in our patient with full recovery and res-
olution of symptoms [3]. Generally, prophylactic removal of MD found
incidentally is still a controversial topic, with one systematic review of
4
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T. Almas et al. Annals of Medicine and Surgery xxx (xxxx) 103734
Table 1
Cases implicating MD as a causative etiology underlying SBO.
Author Year Age Sex Dx Imaging Imaging finding Surgery Follow up Treatment Symptoms
Shelat et al.
[18]
2011 15 F Abd & chest x-
ray and CT of
Abd and pelvis
Mild dilatation of the small
bowels, particularly in the distal
jejunum and proximal ileum
with thickening of the bowel
wall and submucosal oedema.
No transition point was seen on
the CT scan
Exploratory
laparotomy
Alive, no
complications
Segment of the terminal ileum
containing the MD and adhesion band
was resected and stapled anastomosis
with linear staples was performed
Colicky
central
abdominal
pain
associated
with loss of
appetite and
nausea.
Luu et al.
[19]
2016 34 NA CT of Abd and
pelvis
Dilated small bowel loops & non-
propulsive peristalsis and small
bowel obstruction in the right
lower abdominal quadrant
Ileo-ileostomy Alive and
well
Incision of the small intestine and
resection of ileum
Abd pain,
nausea,
vomiting
Ying et al.
[20]
2020 50 M CT of Abd and
pelvis
Several distended and fluid-filled
small bowel loops throughout
the abdomen with a transition
point within the right lower
quadrant suggestive of adhesions
Laparotomy Alive and no
issues on
follow up in
outpatient
clinic
Scarred section of MD and the adjacent
small bowel segment was resected, and
a side-to-side hand-sewn anastomosis
was proceeded
Abd pain,
nausea,
vomiting
Jabri et al.
[21]
2012 26 M CT of Abd and
Abd x-ray
dilated loops of small bowel,
with no free air under either
diaphragm
Laparotomy Alive and
recovered
IV and resection of the MD with closure
of the bowel was performed and
contents of small bowel were drained
into stomach
Abd pain,
nausea,
vomiting
Gunadi et
al. [22]
2021 0.16 F Abd x-ray Small-bowel obstruction Exploratory
laparotomy
Alive and
gradual
recuperation
Segmental small-bowel resection with
primary anastomosis
Abd
distention,
nausea,
vomiting
Gunadi et
al. [22]
2021 5 M Abd x-ray Small-bowel obstruction,
perforated MD and an inflamed
appendix
Small-bowel
resection
Alive and
recovered
gradually
Primary anastomosis and
appendectomy
Abd pain,
nausea,
vomiting
Gunadi et
al. [22]
2021 1.41 F Upper GI Series Found no abnormality in the
upper GI tract
Exploratory
laparotomy
Alive and
gradual
recovery
Segmental small-bowel resection with
primary anastomosis
Abd pain,
nausea,
vomiting
Thakor et
al. [23]
2007 74 M Supine
abdominal x-ray
and CT of
abdomen
Dilated loops of small bowel and
stricture in the terminal ileum of
unknown etiology
Laparotomy Alive and
recovered
MD was divided to release the
obstruction, mobilised and
subsequently removed
Cardinal
symptoms,
abd pain
Ebrahimi et
al. [24]
2021 24 M Abd CT Distal small bowel obstruction Diagnostic
laparoscopy
Alive and
recovered
MD was exteriorized through a
laparotomy and small bowel resection
with a side-to-side stapled anastomosis
was performed.
Crampy
abdominal
pain and
vomiting
Ebrahimi et
al. [24]
2021 56 M Abd CT Distal small bowel obstruction Diagnostic
laparoscopy
Alive and
recovered
MD was exteriorized and tethered to
the mesentery through a band
containing the diverticular blood
supply
Crampy
abdominal
pain,
vomiting
and
obstipation
Almetaher
et al. [25]
2020 37 M Abd CT Small bowel obstruction Laparotomy Alive and
recovered
IV given and small intestinal loops
proximal to the obstruction was
resected together with MD and the
continuity of the bowel was restored
with end-to-end anastomosis
Abd pain
and
vomiting
Bains et al.
[26]
2021 30 F Abd X-ray and
Abd CT
Dilated jejunal and proximal
ileal loops
Laparoscopic
procedure
Alive and
good health
Small midline incision at the umbilicus
and ileo-ileal anastomosis performed
GI bleeding
and acute
Abd pain
Benjelloun
et al. [27]
2009 28 M Supine
abdominal x-
rays and Abd CT
Dilated small-bowel loops with
air-fluid levels and lesion in the
left upper quadrant with dilated
small bowel loops proximally
Laparotomy Alive and
recovered
Intussusception was milked, and
localized ileal resection with MD was
undertaken
Abd pain,
nausea and
bilious
vomiting
Dutta et al.
[28]
2009 55 M Abd X-ray and
CT Abd
Non-obstructive bowel pattern
and complete mid to distal small
bowel obstruction
Laparotomy No follow up
mentioned
MD was exteriorized Mid-lower
and sharp
Abd pain
Nunes et al.
[29]
2009 47 M Ultrasound scan Fluid filled area containing
echogenic components in the
right iliac fossa with a trace of
free fluid surrounding it and
antimesenteric diverticulum
Lower midline
laparotomy
Alive and
recovered
well
Resection of small bowel segment Colicky
central Abd
pain and
diarrhoea
(continued on next page)
5
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T. Almas et al. Annals of Medicine and Surgery xxx (xxxx) 103734
Table 1 (continued)
Author Year Age Sex Dx Imaging Imaging finding Surgery Follow up Treatment Symptoms
Zhang et al.
[30]
2020 45 F Abd CT Focal dilatation and thickening
of the small bowel loop
Exploratory
laparotomy
Alive and
symptom-free
and has
restored
normal
activity and
diet
Adhesiolysis and resection of the MD
with the gangrenous bowel with
anastomosis was performed
Abd pain
accompanied
by nausea
and
vomiting
Ekwunife et
al. [31]
2014 29 M Not mentioned Perforated Meckel's diverticulum
was identified
Segmental ileal
resection
Alive, healthy
but has
superficial
surgical site
infection
IV and antibiotics were given Worsening
Abd pain in
the
umbilicus
region
Pitiakoudis
et al. [32]
2009 18 M CT enteroclysis MD was found 50 cm proximal
to the ileocecal valve
Exploratory
laparoscopy
No follow up
mentioned
MD was resected by tangential excision
using an Endo-Gia-stapler and it was
removed using an Endocath
Abd
discomfort
in right
lower
quadrant,
vomiting
and fresh
blood in his
stools
Bergland
[33]
1963 73 F Abd x-ray Distended small intestinal loops
with multi-level fluid and gas-
filled segments
Diverticulectomy
and anastomosis
No follow up
mentioned
The enterolith was pushed back and
removed from the lumen of the distal
ileum and the proximal ileum was
decompressed by suction
No
symptoms
mentioned
Field [34] 1959 52 M Erect x-ray Marked distention of the small
bowel, absence of gas in the
large bowel. Fluid levels in the
small bowel
Diverticulectomy No follow up
mentioned
Fecalith manipulated proximally to MD Cramping
Abd pains
Christiansen
et al.,
[35]
1967 48 F Abd x-ray Small bowel obstruction with
possible gallstone ileus
Diverticulectomy No follow up
mentioned
MD was exteriorized NA
Marwah et
al. [36]
2016 22 M CECT Abd and
ultrasound
X-ray of Abdomen revealed
multiple air fluid levels and
CECT of the abdomen also
showed dilatation of small gut
loops up to the ileum with distal
ileal stricture
Colonoscopy and
exploratory
laparotomy
No follow up
mentioned
IV, electrolyte replacement, and
nasogastric aspiration and segmental
ileal resection including the strictured
segment and MD was done along with
ileo-ileal anastomosis
Abd
distension
after meals
Tenreiro et
al. [37]
2015 18 M CT of Abd Revealed wall thickening and
air-fluid levels compatible with
small bowel obstruction, without
apparent mechanical cause
Laparotomy Alive,
remained
asymptomatic
Performed a segmental ileal resection
with primary anastomosis
Right lower
quadrant
pain
Capelao et
al. [38]
2017 51 M Abd x-ray and
CT of Abd
Small bowel with air fluid levels
and paucity of gas in the colon
and abrupt stop of the small
bowel without a clear cause
Laparotomy No follow up
mentioned
IV and MD was ligated Abd
distension,
vomitus, and
epigastric
pain
Newme et
al. [39]
2020 24 M X-ray and USG
Abd
Showed distended small bowel
loops and to and fro movement
of bowel loops
Laparotomy No follow up
mentioned
Terminal ileum was constricted and
indurated; MD was untwirled and
segmental resection of the necrosed
terminal ileum and Meckel's
diverticulum were done
Acute abd
pain and
vomiting
Sarkardeh
and Sani
[40]
2020 92 F Abd X-ray Small bowel with air-fluid levels
and dilated bowel loops
Laparotomy No follow up
mentioned
IV and Segmental small bowel resection
including the diverticulum was
performed with a primary end to end
anastomosis
Abd pain,
vomitus, and
distention
Jabri and
Sherbini
[41]
2012 26 M Abd x-ray and
CT of Abd
Dilated loops of small bowel,
with no free air under either
diaphragm and stricture in the
ileum and collapse of the distal
ileum and large bowel
Laparotomy Alive, no
complications
IV and during surgery the meso-
diverticular band was separated from
the mesentery, the ileal loop was
released from the diverticulum.
Resection of the Meckel's diverticulum
with closure of the bowel was
performed. The small bowel was then
decompressed, and the content was
gently milked into the stomach before
being aspirated via the nasogastric tube
Abd pain,
vomitus, and
distention
(continued on next page)
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T. Almas et al. Annals of Medicine and Surgery xxx (xxxx) 103734
Table 1 (continued)
Author Year Age Sex Dx Imaging Imaging finding Surgery Follow up Treatment Symptoms
Takura et
al. [42]
2021 56 F Abd CT Small intestine was generally
dilated, and there was a closed
loop-like appearance near the
end of the ileum and
surrounding fatty tissue opacity.
A strangulated bowel obstruction
was suspected
Laparotomy Alive, good
progress
MD was resected Abd pain
and
vomiting
Sumer et al.
[43]
2010 17 M Abd x-ray Small intestine exhibited an air
fluid level
Exploratory
laparotomy
Alive,
recovered
well
Resection of the MD Abd pain
and
vomiting
Yazgan et
al. [44]
2016 35 M Abd x-ray and
CECT of Abd
Markedly dilated loops of the
middle and distal small bowel
with multiple air-fluid levels.
Tubular fluid containing
structure found in LQ, deemed
MD. Collapsed distal ileum
Laparotomy Alive, no
complications
Segmental resection and primary end-
to-end anastomosis were performed
Abd pain,
vomiting
and nausea.
Abdomen
distended.
Bouassida et
al. [45]
2011 22 M Abd x-ray Displayed air fluid levels of the
small bowel, no
pneumoperitoneum. Diagnosed
as an acute small bowel
obstruction.
Laparotomy Alive, no
complications
Segmental small bowel resection and
hand-sewn anastomosis was performed
Abd pain
and
vomiting.
Abd was
hard &
tender
Ying and
Yahng
[46]
2020 50 M Abd & chest x-
ray CT of Abd
and pelvis
Dilated stomach and multiple
air-fluid levels respectively.
multiple markedly distended and
fluid-filled small bowel loops
throughout the abdomen with a
transition point within the right
lower quadrant suggestive of
adhesions
Laparotomy Alive, no
complications
Extensively scarred section of MD along
with the adjacent small bowel segment
was resected and a side-to-side hand-
sewn anastomosis
Vomiting,
abdominal
pain and
distension
Murruste et
al. [47]
2014 41 M Abd CT Markedly dilated small-bowel
loops with multiple air-fluid
levels
Laparotomy Alive, no
complications
Approximately 20 cm of the small
bowel with Meckel's diverticulum was
resected
Crampy and
intermittent
abdominal
pain, nausea
and
retention of
stool and
gases
Ramnath et
al. [48]
2018 16 F Erect X-ray Abd
& CT Abd
Narrow lumen of terminal ileum
two feet from ileo-cecal junction
Exploratory
laparotomy
Alive, no
complications
Release of constricting band and
resection of diverticulum along with
segment of ileum was done and end to
end anastomosis of ileum was done.
Abd pain,
vomiting
and
constipation
Skarpas et
al. [49]
2020 63 F Abd x-ray and
CT of Abd
Small bowel obstruction Exploratory
laparotomy
Alive, no
complications
MD band caused obstruction by
trapping of bowel loop. After
separating the band from the
mesentery, the ileal loop was released
from the diverticulum. Resection of the
Meckel's diverticulum and closure of
the bowel were done using a TA
stapler.
Distended
Abd, pain in
the lower
right
abdominal
quadrant,
fever 37 °C
Gupta and
Singh
[50]
2011 32 M Ultrasonography
(USG) of the
Abd, Erect Abdo
x-ray
Revealed hyperperistaltic dilated
small bowel loops and multiple
air fluid levels situated in the
central abdomen and to the left
Exploratory
laparotomy
Alive, no
complications
MD and adhesion were excised, and the
small bowel freed and decompressed.
Abd pain,
nausea,
vomiting
Arslan et al.
[51]
2020 63 M Erect X-ray Abd
& CT Abd
Few distended small bowel loops
and multiple air-fluid levels. CT
showed fluid accumulation in
the intestinal loops and local
dilatation, favoring an
obstruction
Exploratory
laparotomy
Alive, no
complications
A 15 cm segmental small intestine was
resected, including the MD and the
inflammatory and fragile mesentery of
the bowel loops. Then, double end-to-
end anastomosis was performed
manually.
Abd pain,
nausea,
vomiting
Cartanese et
al. [52]
2011 42 M CECT Abd and
ultrasound
A transition point between
dilated and collapsed small
bowel in the right lower
quadrant consistent with a high-
grade small bowel obstruction
was found.
Exploratory
laparotomy
Alive, no
complications
The diverticulum was resected using a
GIA stapler, without small bowel
resection
lower
quadrant
and
suprapubic
pain and
several
episodes of
vomiting
without
flatus.
(continued on next page)
7
CORRECTED PROOF
T. Almas et al. Annals of Medicine and Surgery xxx (xxxx) 103734
Table 1 (continued)
Author Year Age Sex Dx Imaging Imaging finding Surgery Follow up Treatment Symptoms
Zorn et al.
[53]
2022 30 M Abd & chest X-
ray. CT of Abd
Showed dilated loop sof small
bowel and a distal high-grade
SBO with multiple dilated loops
of small bowel throughout the
abdomen measuring up to 3.5
cm in diameter. Mild Ascites
Exploratory
laparotomy
Alive, no
complications
A segmental small bowel resection with
hand sewn primary anastomosis was
performed.
Abd pain,
vomiting
and nausea
Malderen
and
Camilleri
[54]
2018 49 F CT of Abd 15-cm long dilated segment,
diagnosed as localized ileal
dilatation close to the Meckel's
diverticulum
Laparotomy No follow up
mentioned
resection of the Meckel's diverticulum
and appendix
Bloody
stools
Kuru et al.
[55]
2013 17 M Abd x-Ray and
USG
Mildly distended small bowel
loops. Dilated small bowel loops
with a small amount of fluid in
the right lower quadrant
Exploratory
laparotomy
Alive,
recovered
well
MD was resected along the flange of
ileum that encompassed the vascular
territory of inflamed and friable
mesentery. A manual two-layer, end-to-
end anastomosis was performed to
restore the continuity of the small
bowel
Abd pain,
nausea,
vomiting
Marascia
[56]
2019 29 F Abd x-ray and
CT of Abd
Diffuse distention of small bowel
loops without evidence of free
gas within the peritoneum. high-
grade distal SBO with transition
point in the left iliac fossa and
signs suggestive of ileo-ileal
intussusception
Diagnostic
laparotomy
Alive, no
complications
A segmental resection of the distal
ileum 10 cm proximal to the cecum
with a side-to-side anastomosis was
performed
Abd pain
with
associated
vomiting,
abdominal
bloating,
constipation,
and anorexia
Benhamou
[57]
1979 78 M Abd x-ray Small bowel obstruction with
opacity in the right iliac fossa
Laparotomy No follow up
mentioned
Diverticulectomy No
symptoms
mentioned
Hayee et al.
[58]
2003 79 F Abd x-ray Opacity on the left side
Gastro-graffin study: numerous
small bowel diverticula of
varying sizes and minimal
passage of barium beyond the
mid-jejunum
Enterotomy No follow up
mentioned
The stone was found impacted in the
middle of the jejunum and was
removed via a small enterotomy
No
symptoms
mentioned
DiGiacomo
et al. [59]
1993 9 M Abd x-ray Local ileus, multiple dilated
bowel loops
Appendectomy
and
diverticulectomy
No follow up
mentioned
Fecalith was manipulated distally to the
cecum
No
symptoms
mentioned
MD: Meckel's diverticulum.
SBO: Small bowel obstruction.
Abd: Abdominal.
244 cases divulging reduced postoperative consequences for uncompli-
cated and asymptomatic Meckel's Diverticulum left alone [13].
In order to better elucidate the etiology underlying the obstructive
symptoms seen in our case, we conducted a literature search using the
digital databases (PubMed/MEDLINE, CINAHL, and Web of Science) to
search for relevant material and articles implicating MD as a cause of
SBO. The literature search in our search was conducted using the terms
(s): small bowel obstructionAND meckel's diverticulumOR diver-
ticulitisOR volvulusOR intussusception. The symptomatology,
imaging findings, treatment employed, and the follow-up are delin-
eated by Table 1 below [1859].
4. Limitations
The present study discusses a case report and delineates a single-
center experience dealing with an unusual etiology underlying acute
small bowel obstruction. While the study yields important evidence sur-
rounding this etiology and prompts the clinicians to aptly recognize this
congenital aberration as a cause of acute small bowel obstruction, it is
limited by its sample size. Further multi-centric cross-sectional studies
evaluating the true, unadjusted incidence of MD as the causative etiol-
ogy underlying acute small bowel obstruction will further yield robust
data to support the presented conclusions.
5. Conclusion
MD is the most common congenital abnormality of the gastrointesti-
nal tract, presenting in 13% of patients, of which about 4% may be-
come symptomatic. When asymptomatic, it is discovered incidentally
during surgical exploration or through diagnostic imaging. Various he-
morrhagic, inflammatory, and obstructive complications can arise,
leading to an array of presentations. Nevertheless, the presence of MD
as the causative etiology underlying acute SBO remains a clinical
enigma, with most cases erroneously attributed to post-operative adhe-
sions and/or abdominal hernias. Early diagnosis and a high index of
suspicion are imperative to deliver the most optimal treatment. Al-
though relatively rare in adults, MD should be considered in the list of
differentials in patients with intussusception leading to SBO, especially
on a background history unremarkable for the most common etiologies
causing SBO.
Disclosure
None.
Provenance and peer review
Not commissioned, externally peer-reviewed.
Ethical approval
NA.
Sources of funding for your research
NA.
8
CORRECTED PROOF
T. Almas et al. Annals of Medicine and Surgery xxx (xxxx) 103734
Author contribution
TA, AKA, DA, MU, ESA: conceived the idea, designed the study, and
drafted the manuscript.
KA, MA, TA, OK, MA, EA: conducted comprehensive literature
search, screened the studies for relevant content, and created the litera-
ture review table.
AS, MO, FSA, MK: revised the manuscript critically and refined the
literature review table.
AB, MMA, MS, RA: drafted the discussion part of the manuscript, re-
vised the final version of the manuscript critically based on the re-
viewer and editorial comments.
TA, SH, MFM, EM: Conceived the initial study idea, diagnosed the
case, and gave the final approval for publication.
Registration of research studies
Name of the registry: NA
Unique Identifying number or registration ID: NA
Hyperlink to your specific registration (must be publicly accessible
and will be checked): NA
Consent
Written informed consent was obtained from the patient for publica-
tion of this case report and accompanying images. A copy of the written
consent is available for review by the Editor-in-Chief of this journal on
request.
Guarantor
Talal Almas.
RCSI University of Medicine and Health Sciences.
123 St. Stephen's Green.
Dublin 2, Ireland.
Talalalmas.almas@gmail.com.
Declaration of competing interest
NA.
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10
... Flange with Acute Intestinal Obstruction and Midgut Volvulus: A Case Report been recently subjects of literature reviews. 3,4) However, internal hernias and midgut volvulus are two rare entities. 2,5,6) The interest of this case lies in the exceptional and rare character of the observed association: MD mimicking a postoperative flange complicated by acute intestinal obstruction, and IM by midgut volvulus. ...
... 4,5) Preoperative diagnosis of complicated MD and IM is difficult as it mimics other common acute abdominal conditions; the clinical presentation can often be atypical. 3,10) Indeed, these two congenital malformations are generally discovered intraoperatively. 3,5,11) In this case, classic obstructive syndrome presents a diagnostic and therapeutic challenge, especially for having MD, midgut volvulus, and acute appendicitis. ...
... 3,10) Indeed, these two congenital malformations are generally discovered intraoperatively. 3,5,11) In this case, classic obstructive syndrome presents a diagnostic and therapeutic challenge, especially for having MD, midgut volvulus, and acute appendicitis. Usually, symptoms include persistent nausea, biliary vomiting, abdominal distension, absolute constipation, and sometimes painless gastrointestinal bleeding. ...
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INTRODUCTION: The interest of this case lies in the exceptional and rare character of the observed association.: Meckel’s diverticulum (MD) mimicking a postoperative flange complicated by acute intestinal obstruction and malrotation by midgut volvulus. CASE PRESENTATION: A 17-year-old black male student, with a body mass index of 28 kg/m² was admitted to the emergency department of a 4th category rural hospital, with paroxystic abdominal pain and vomiting. Medical history revealed an abdominal surgery for an umbilical hernia 3 years earlier. There was no malformation such as imperforate anus, Hirschsprung's disease, esophageal tracheal fistula, or cardiac anomaly in the medical history. An abdominal X-ray confirmed an acute intestinal obstruction showing hydroaeric levels. The diagnosis of acute intestinal obstruction on a flange was retained. A median laparotomy was performed; a solid mass-like lengthy structure mimicking postoperative flange was seen associated with midgut volvulus, while a malposition of the intestine was observed with a mesenteric band, as well as a hyperemic appendix. A 90° rotation stop of the midgut also called a complete common mesentery was in place; we then carried out a Ladd procedure. Morpho-pathological examination of the surgical specimens revealed the following: richly vascularized fibro-adipose tissues with no evidence of malignancy in the diverticular specimen, and acute pan-appendicitis with no evidence of malignancy in the appendicular specimen. The patient started to ingest food orally on the third postoperative day, and he was discharged uneventfully on the fifth day. CONCLUSION: MD, although generally a tubular structure, may sometimes appear as a non-tubular mass during clinical examination. Intestinal obstruction due to MD associated with midgut volvulus is exceptional. Management of this association should be based on accurate knowledge of the morpho-embryological specificities during gut development.
... La tomografía computarizada de abdomen y pelvis podría mostrar inflamación u obstrucción en el divertículo, e incluso la angiografía podría identificar la fuente de hemorragia gastrointestinal y la arteria vitelina, remanente de la arteria onfalomesentérica. 10 La prueba más sensible es la gammagrafía con radionúclidos (gammagrafía de Meckel), un estudio nuclear que se realiza mediante la administración de tecnecio-99m, el cual es absorbido por la mucosa gástrica heterotópica permitiendo la visualización del DM, con una sensibilidad del 85% y una especificidad del 95%; 11 sin embargo, hay estudios que reportan una sensibilidad baja, de hasta el 15,3%. 6 La absorción del contraste se puede mejorar usando cimetidina, ranitidina o glucagón. ...
... 6 La absorción del contraste se puede mejorar usando cimetidina, ranitidina o glucagón. 11 Los hallazgos de la gammagrafía pueden estar influenciados por varios factores, como hemorra-gia, inflamación y malformaciones vasculares del tracto gastrointestinal; además, no todos los divertículos contienen tejido ectópico que absorbe el tecnecio, y su disponibilidad en todos los centros limita su uso generalizado. 11 La visualización directa del DM es la forma de realizar un diagnóstico preciso; esto podría realizarse por medio de laparoscopía y laparotomía diagnóstica, o a través de endoscópica del intestino delgado, como la enteroscopía de doble balón y la VCE. ...
... 11 Los hallazgos de la gammagrafía pueden estar influenciados por varios factores, como hemorra-gia, inflamación y malformaciones vasculares del tracto gastrointestinal; además, no todos los divertículos contienen tejido ectópico que absorbe el tecnecio, y su disponibilidad en todos los centros limita su uso generalizado. 11 La visualización directa del DM es la forma de realizar un diagnóstico preciso; esto podría realizarse por medio de laparoscopía y laparotomía diagnóstica, o a través de endoscópica del intestino delgado, como la enteroscopía de doble balón y la VCE. ...
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El divertículo de Meckel es una anomalía congénita común del intestino delgado causada por la falta de cierre completo del conducto onfalomesentérico. La mayoría de los pacientes no presentan síntomas y su diagnóstico se realiza de forma incidental en estudios de imágenes médicas. El síntoma más común es el sangrado rectal indoloro, pero puede presentar-se de diferentes formas. Existen varias herramientas diag-nósticas para el divertículo de Meckel sintomático, como la gammagrafía de Meckel, pero la forma más precisa de diagnosticarlo es a través de la visualización directa, como la videocápsula endoscópica, que es útil para determinar la causa de la hemorragia en el intestino delgado.
... This usually occurs in the fifth week of developmentand causes a true outpouching of the small intestine, located approximately two feet from the ileocecal valve. It is the most common congenital abnormality afflicting the gastrointestinal tract and has been reported in up to 1 -3% of patients [5] MD is a true diverticulum involving all layers of the intestinal wall. Typically occurs within 100 cm proximal to the ileocecal valve on the antimesenteric border. ...
... · It is two times more likely to be symptomatic in males than females, and · 2% become symptomatic (however, most Meckel's diverticula are clinically silent). [4] The However, hemorrhagic, inflammatory, and obstructive complications can arise [5] It presents only when some complication arises. In order of frequency, the complications are: [9] Hemorrhage: It occurs due to peptic ulceration and is the most common cause for painless major ...
... Approximately 4 % of patients experienced one or more complications (Table 1) [9]. Small bowel obstruction and diverticulitis are the most common problems in Meckel's diverticulum due to heterotopic pancreatic or gastric tissue [10]. ...
... Small bowel obstruction and diverticulitis are the most common problems in Meckel's diverticulum due to heterotopic pancreatic or gastric tissue [10]. The strangulation due to a mesodiverticular band trapping around the small bowel or other problems (intussusception, volvulus) caused a bowel obstruction, which led to an intestinal emergency [9]. ...
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Introduction and Importance: Meckel's diverticulum is a rare congenital condition often detected incidentally. Meckel's diverticulum, a rare disease, may result in acute intestinal obstruction and is frequently misdiagnosed. This study aims to report a case of acute intestinal obstruction due to Meckel's diverticulum. Case presentation A 61-year-old Javanese man was admitted to the emergency room with a history of constipation, nausea, vomiting, and abdominal pain. Physical examination showed abdomen distention, tenderness in the lower quadrant, and hyperactive bowel sound. Rectal examination found that the rectal ampulla was collapsed. A plain abdominal Radiograph showed small bowel dilatation and air-fluid levels. The patient was diagnosed with small bowel obstruction due to suspected left-sided colon cancer and taken up for exploratory laparotomy. Clinical discussion On exploration, Meckel's diverticulum measuring 3.5 cm in length and with a 2 cm base was found about 70 cm proximal to the Bauhin valve; the thin part formed a band that entangled the small bowel. Ileo-ileal resection anastomosis was performed. Clinical discussion Meckel's diverticulum is an intestinal pouch caused by incomplete obliteration of the vitelline duct during gestation. This condition affects 2 % of the population and is within 2 feet of the Bauhin valve. The mesodiverticular band was found to be the source of the bowel obstruction. Surgical resection is required for complicated diverticulum. Conclusion Meckel's diverticulum can be difficult to diagnose and require a higher level of suspicion. Although Meckel's diverticulum is uncommon in adults, it should be considered a cause of small bowel obstruction.
... Intestinal obstruction, Malena or hematochezia, and inflammation are major symptoms [2]. Meckel's diverticulum (MD) is the most common congenital anomaly of the gastrointestinal tract that ensues as a result of partial closure and persistence of the vitelline, or the omphalomesenteric duct during embryogenesis [3]. It is a true diverticulum containing all the layers of the small intestine and is known to contain ectopic gastric mucosa [4]. ...
Article
Meckel’s diverticulum (MD) is a congenital outpouching or bulge in the lower part of the small intestine. It is the most common congenital defect of the gastrointestinal tract. MD is usually asymptomatic but when symptomatic, typically presents in childhood. Meckel’s diverticulum is the most common congenital anomaly of the gastrointestinal system. It originates from failure of the vitelline duct to obliterate completely, which is usually located on the antimesenteric border of the ileum. Its incidence is between 1% and 3%. Meckel’s diverticulum occurs with equal frequency in both sexes, but symptoms from complications are more common in male patients. Most of the Meckel’s diverticula are discovered incidentally during a surgical procedure performed for other reasons. Hemorrhage, small bowel obstruction, and diverticulitis are the most frequent complications. This case was a 75 years old male with abdominal pain and signs and symptoms of acute appendicitis that in surgery has a complicated Meckel's diverticulum that resected and anastomosis of small intestine was done and discharge with no complication and healthy. In summary, although Meckel’s diverticulum is the most prevalent congenital abnormality of the gastrointestinal tract; it is often difficult to diagnose. The complications of Meckel’s diverticulum should be taken into account in the differential diagnosis of small bowel obstruction. Surgical resection has always been the treatment of choice in symptomatic MD. However, there has been debate about the proper management of asymptomatic MD if incidentally discovered during laparotomy or laparoscopy. Fewer studies discouraged the prophylactic removal of MD.
... Common complications associated with Meckel's diverticulum include gastrointestinal bleeding, diverticulitis, and intestinal obstruction [2]. In older adults, intestinal obstruction due to Meckel's diverticulum is exceedingly rare, with only a limited number of cases reported in the medical literature [3][4][5][6][7][8]. ...
Article
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Meckel’s diverticulum is a congenital anomaly resulting from incomplete obliteration of the omphalomesenteric duct during embryonic development. While it is the most common congenital anomaly of the gastrointestinal tract, clinical manifestations are relatively rare and may include gastrointestinal bleeding, diverticulitis, or intestinal obstruction. We present a unique case of a 55-year-old Chinese male patient who presented with features of small bowel obstruction due to adhesion caused by Meckel’s diverticulum. He was treated with exploratory laparotomy and has recovered well. Complications arising from Meckel’s diverticulum are rare but more common in the paediatric population. Most patients present with gastrointestinal bleeding, with a small minority presenting with intestinal obstruction symptoms such as nausea, vomiting, or abdominal pain. The work-up of the patient should include thorough history taking, examination, and abdominal imaging such as a CT scan. This case report highlights the importance of considering Meckel’s diverticulum as a potential cause of intestinal obstruction in adults. Prophylactic resection of Meckel’s diverticulum in adults should be considered if potential complications such as adhesional intestinal obstruction are foreseen.
... More often, it has a strangulation character in the form of a volvulus of the small intestine around a fixed diverticulum or there is an internal strangulation of the intestinal loops. The main manifestations are abdominal pain, vomiting, flatulence [9][10][11][12][13][14]35]. ...
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Introduction. Meckel's diverticulum (MD) is a congenital anomaly of the gastrointestinal tract. In most cases, uncomplicated DM is silent. It is mainly diagnosed when complications arise or accidentally during diagnostic procedures or surgical interventions. A recognised effective diagnostic method is laparoscopy, which allows to assess the localisation and degree of pathological changes in the diverticulum. Treatment of complicated DM is surgical. The volume of surgery depends on the diameter of the diverticulum, the nature of complications, the prevalence of the inflammatory process at the base of the diverticulum and the ileum wall, and the spread of peritonitis. In this report, we would like to share our own successful experience of treating a patient with DM complicated by necrosis and volvulus of the small intestine. Case report. A 42-year-old male patient was hospitalised with complaints of abdominal pain, fever up to 38°C, and nausea. During the examination, the abdomen was distended, painful in all parts, spared during breathing. In the right iliac region and in the right lateral canal, there were weakly positive symptoms of peritoneal irritation, peristalsis was weakened. Ultrasound examination of the abdominal cavity revealed free fluid in the right hypochondrium and pelvic cavity, dilatation of the small intestine loops. Plain radiography of the abdominal cavity: pneumatosis of the intestine, small intestinal fluid levels. Video laparoscopy was performed to clarify the diagnosis under endotracheal anaesthesia. During the revision of the abdominal cavity, a defect of up to 5.0 cm in the mesentery of the small intestine with a large-sized and necrotic altered DM and a wrap around it of small intestinal loops with necrosis was detected. Resection of the necrotic loops of the small intestine with DM was performed with the application of a «side-to-side» intestinal anastomosis. The postoperative period was uneventful. The patient was discharged on day 10. Discussion. Due to the lack of characteristic symptoms, the diagnosis of DM, even in cases of complications, is sometimes established late, which entails problems in the further treatment of patients. Today, laparoscopy is the leading and most informative method in the diagnosis of DM. In some cases, it is the first stage of surgical intervention. Intestinal obstruction is one of the most common complications of DM. It is caused by small intestine torsion around a fixed diverticulum, nodule formation, and diverticulum invasion. Early diagnosis is important because delayed surgery increases mortality. We present a clinical case of complicated DM with symptoms typical of small bowel obstruction. The standard methods used at the first stage of diagnosis did not allow to establish the cause of intestinal obstruction. Only the use of laparoscopy made it possible to establish an accurate diagnosis. To date, the question of the need to remove an accidentally found DM remains unresolved. It is believed that an individual approach is advisable. In cases of complications, the choice of surgical intervention depends on the diameter of the diverticulum base, the severity of morphological changes in its wall and the wall of the small intestine. Conclusions. The absence of specific symptoms and low informational content of routine diagnostic methods are the reason for the untimely diagnosis of DM, which often causes the development of severe complications. Laparoscopy is the only significant diagnostic and treatment method that allows for an accurate diagnosis and, in some cases, diverticulectomy. An individual approach is recommended in the treatment of DM, depending on the clinical situation.
... 11 Delayed diagnosis of MD spells doom as it may result in significant morbidity and mortality. Its early recognition is imperative since a delay in surgery of thirty-six (36) hours or more can triple the mortality rate from 8% to 25% in patients featured with strangulation 10 . Therefore, surgeons/clinicians must be intentional about MD, its presentation, and the best practices for its diagnosis and management. ...
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Introduction: Most cases of Meckel’s Diverticulum (MD) are asymptomatic and when symptomatic, preoperative diagnosis of MD maybe a dilemma. Intestinal obstruction is a major complication in the adult population. Case presentation: We report a case of a 24-year-old female presenting with intestinal obstruction from Meckels Diverticulum. Conclusion: MD is largely asymptomatic in adults, however may be present and should be included in our array of differential diagnoses.
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Introdução: O divertículo de Meckel é uma condição rara que decorre de uma anormalidade do processo embrionário, resultando em uma estrutura abdominal que pode provocar desfechos clínicos importantes nos pacientes. Objetivo: O presente estudo teve como objetivo avaliar os aspectos clínicos, epidemiológicos e fisiopatológicos do divertículo de Meckel e suas complicações, alicerçando a construção do conhecimento com base em relatos de casos e no conhecimento sedimentado na literatura. Materiais e Métodos: Trata-se de uma revisão integrativa de literatura acerca das características clínicas gerais sobre o divertículo de Meckel e suas complicações. Utilizou-se a estratégia PICO para a elaboração da pergunta norteadora. Ademais, realizou-se o cruzamento dos descritores “Divertículo de Meckel”; “Complicações”; “Propedêutica”, nas bases de dados National Library of Medicine (PubMed MEDLINE), Scientific Eletronic Library Online (SCIELO), Ebscohost, Google Scholar e Biblioteca Virtual de Saúde (BVS). Resultados e Discussão: Os artigos demonstraram que a ocorrência do divertículo de Meckel está mais associada ao sexo masculino e em pacientes pediátricos. Também foram discutidos os mecanismos fisiopatológicos para o seu desenvolvimento, bem como as principais manifestações clínicas e as formas diagnósticas. Conclusão: Nesse contexto, o divertículo de Meckel é, na maioria das vezes, uma condição benigna que cursa com sintomatologia de abdome agudo e suas variedades. O diagnóstico é eminentemente clínico e complementado por exames de imagem. O tratamento engloba medidas de analgesia para o controle do quadro agudo e ressecção cirúrgica como opção terapêutica definitiva.
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Most of Meckel's diverticulum (MD) are asymptomatic but when clinical manifestations arise from complications like acute intestinal obstruction, MD must be included in the differential diagnosis. Early surgery is required to prevent strangulation or gangrene.
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Small bowel obstruction (SBO) secondary to intussusception of Meckel’s diverticulum (MD) is a rare cause of acute abdominal pain that may warrant urgent surgical treatment. Volvulus or intussusception of the small bowel with presence of MD as the lead point is the most commonly reported etiology of Meckel’s related obstructions. We report an interesting case of a small bowel obstruction caused by the intussusception of an MD within its own lumen. The case involves a 30-year-old male who presented to the emergency room with acute, severe abdominal pain with an abdominal computed tomography (CT) showing a distal high-grade SBO. Decision was made to take the patient to the operating room urgently due to his clinical examination and radiologic imaging, specifically CT scan. Diagnostic laparoscopy was performed and subsequently converted to an exploratory laparotomy, which revealed the intussuscepted MD with focal necrosis into the distal small bowel causing an SBO. A segmental small bowel resection with hand sewn primary anastomosis was performed. The case presents an interesting challenge in deciding when to take a patient with an SBO to the operating room versus initial conservative management and what the treatment should be if an MD is encountered. In addition, the case emphasizes the importance of history and physical exam findings in coordination with radiologic imaging in helping to make appropriate decisions in a timely manner for operative vs conservative management of an SBO. It reminds us that, Meckel’s diverticulum, although less commonly the cause of a small bowel obstruction in the adult population, needs to be on the differential diagnosis and we need to have a high clinical suspicion for this possibility to ensure appropriate treatment in a timely manner.
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Introduction: Mesodiverticular band (MDB) is a rare congenital intestinal malformation. It originates from the embryonic remnant of the vitelline artery and is usually associated with Meckel’s diverticulum (MD). Persistent MDB may cause small bowel obstruction by trapping a loop of the bowel, hemoperitoneum due to aneurysmal or traumatic rupture of MDB. The purpose of this article is to review the literature of MDB and identify the patterns of presentation, complications, and management options. Methods: We searched PubMed for articles containing terms: “Mesodiverticular band,” “Vitelline band,” and “Vitelline artery remnant.” Abstracts were reviewed in detail and we included all the case reports available in full-text and in English language. We excluded all case reports of patients younger than 18 years of age. Results: Only 20 case reports were included. Only adult patients were included. The male to female ratio was 3:1. The most common presentation was small bowel obstruction followed by hemoperitoneum. The majority required exploratory laparotomy with more than half requiring small bowel resection. One death report secondary to undiagnosed internal hernia. Conclusion: MDB with MD is a rare cause of intestinal obstruction or hemoperitoneum in adults. It remains a diagnostic dilemma as it is usually diagnosed intraoperatively.
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Introduction We report a case of a patient who underwent laparoscopic surgery for intestinal obstruction caused by the mesodiverticular band of Meckel's diverticulum, with pathological specimens showing ectopic pancreas. Presentation of case A 56-year-old woman presented to our hospital with complaints of abdominal pain and vomiting. Upon close examination, we suspected strangulated intestinal obstruction, and performed an emergency surgery. An internal hernia with a band leading to a Meckel's diverticulum was noted. Focusing on the attachment of the band, leading to the Meckel's diverticulum, we suspected a mesodiverticular band and deemed it necessary to be resected. Surgery was completed with resection of the band to relieve the intestinal obstruction, with simultaneous resection of the Meckel's diverticulum. It was necessary to resect Meckel's diverticulum simultaneously for histopathological examination. Histopathological examination revealed a mesodiverticular band in the resected band and ectopic pancreas in the Meckel's diverticulum. Discussion We chose to perform a complete laparoscopic resection because of the presence of simple intestinal obstruction caused by mesodiverticular bands or diverticula. We believe that small laparotomy can be opted in less severe cases, regardless of laparoscopic completion. Conclusion We suspected adherent bowel obstruction and detected a band. We focused on band attachment and determined that the band should be resected if it was attached to Meckel's diverticulum. The resection method should be carefully selected, and the specimen should be histopathalogically examined.
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Background: Meckel diverticulum (MD) is the most common congenital anomaly of the intestines, with an incidence of 2% of the general population. It can present as various clinical features with complications and be life threatening if diagnosis is delayed and treatment late. Case Presentation: We report three pediatric cases with complicated MD: one female presented with small-bowel obstruction, one male with peritonitis, and one female with severe iron-deficiency anemia, without gross gastrointestinal bleeding nor any ectopic gastric mucosa. All patients underwent exploratory laparotomy, segmental small-bowel resection, and primary anastomosis. They successfully recovered and were uneventfully discharged on the fourth, seventh, and 10th postoperative days, respectively. Conclusions: MD can present with various complication spectrums, including small-bowel obstruction, peritonitis, and severe iron-deficiency anemia, which may cause difficulty in definitive diagnosis, particularly in children. Segmental small-bowel resection and primary anastomosis are effective surgical approaches and show good outcomes for MD patients.
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Background Inverted Meckel’s diverticulum refers to the condition in which the diverticulum inverts on itself. The reasons for such an inversion are poorly understood due to the rarity of the condition. We present a case of inverted Meckel’s diverticulum, an uncommon finding, as a cause of recurrent intussusception. Case presentation A 30-year old Indian woman presented with complaints of pain in the central abdomen for 3 days, accompanied with vomiting and loose stools. Computed tomography images were suggestive of intussusception with intestinal obstruction. Intra-operative findings were suggestive of an intussuscepted segment of ileum measuring 10 cm in length, proximal to ileocecal junction. Ileo–ileal anastomosis was performed after appropriate resection. Upon opening the specimen, we were surprised to find an inverted Meckel diverticulum with lipoma at one end causing the intussusception. The patient made an uneventful recovery and was discharged after 5 days. Conclusion The reasons for inversion include abnormal peristalsis around the diverticulum and non-fixity of the diverticulum itself. The inverted diverticulum itself can cause luminal compromise and acts as a lead point for intussusception leading to obstruction. Computed tomography remains the diagnostic tool of choice for identifying intestinal obstruction and intussusception. Although pathological signs, such as lipoma, can be identified, the identification of any inversion will require a proficient radiologist. Inverted Meckel’s diverticulum is a rare condition which is difficult to diagnose preoperatively. Treatment is surgical, whether diagnosed pre-operatively or intra-operatively, and includes segmental resection and anastomosis. This uncommon condition should be noted as one-off differential diagnosis for intussusception and intestinal obstruction.
Article
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We present two rare cases of small bowel obstruction (SBO) secondary to Meckel’s diverticulum (MD) where the mechanism of obstruction was not readily apparent. Both were cases of virgin abdomen with pre-operative CT scans demonstrating SBO without a clear underlying cause or mass. Diagnostic laparoscopy was performed, which established the underlying cause to be MD, and laparoscopic-assisted resection was undertaken to resect small bowel and perform a side-to-side stapled anastomosis. We subsequently describe the different mechanisms by which MD can cause obstruction as described in the literature.
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Background Meckel’s diverticulum (MD) is the commonest congenital abnormality of the gastrointestinal tract that occurs in 2% of general population. It remains asymptomatic, but it may lead to life-threatening complications. These complications may be misdiagnosed with other gastrointestinal disorders like acute appendicitis, making its diagnosis challenging among pediatricians and pediatric surgeons. In this study, we reported five cases with different presentations of complicated MD in children. Results Five patients with different presentations of MD were reported during the period from January 2016 to January 2020. Patients’ demographics, clinical presentations, investigations, operative data, and postoperative outcome were recorded and analyzed. Conclusions The present study highlights different presentations of MD. Surgical interference is the main key of treatment of symptomatic MD either by wedge resection of a small base diverticulum or by resection anastomosis of the small intestine in wide base and inflamed diverticulum.
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Introduction: The SCARE Guidelines were first published in 2016 and were last updated in 2018. They provide a structure for reporting surgical case reports and are used and endorsed by authors, journal editors and reviewers, in order to increase robustness and transparency in reporting surgical cases. They must be kept up to date in order to drive forwards reporting quality. As such, we have updated these guidelines via a DELPHI consensus exercise. Methods: The updated guidelines were produced via a DELPHI consensus exercise. Members were invited from the previous DELPHI group, as well as editorial board member and peer reviewers of the International Journal of Surgery Case Reports. The expert group completed an online survey to indicate their agreement with proposed changes to the checklist items. Results: 54 surgical experts agreed to participate and 53 (98%) completed the survey. The responses and suggested modifications were incorporated to the 2018 guideline. There was a high degree of agreement amongst the SCARE Group, with all SCARE Items receiving over 70% scores 7-9. Conclusion: A DELPHI consensus exercise was completed, and an updated and improved SCARE Checklist is now presented.
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Meckel’s Diverticulum is a sac-like protrusion of the intestinal wall. It is located at 40–60 cm from the caecum. In the majority of cases, Meckel’s Diverticulum is clinically silent, while complications are found in 4% of the population. Complicated diverticulitis is associated with the formation of abscess, fistula, bowel obstruction or frank perforation. We present a case of a 63-year-old woman with a distended abdomen, pain in the lower right abdominal quadrant, fever 37°C and where emergency exploratory laparotomy revealed that obstruction was caused by a bowel loop trapped by a mesenterium-diverticular band.
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Reporting herewith 2 cases of Meckel's diverticulum presenting with acute intestinal obstruction. The patients were managed surgically. The cases were presented in emergency department and management were based on clinical and imaging after a initial resuscitation. The intra-operative findings are discussed in herewith.