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Presacral Schwannoma Resected Via Anterior Trans Peritoneal Approach: A Case Report

Authors:
  • Pai Onco Care Centre, Hubli,, Karnataka, India.
Gastroenterology & Hepatology: Open Access
Presacral Schwannoma Resected Via Anterior Trans
Peritoneal Approach: A Case Report
Volume 3 Issue 2- 2015
1Department of Surgical Oncology, Kerudi Cancer Hospital and
Research Centre, Bagalkot, Karnataka, India
2Department of Radiodiagnosis, Kerudi Cancer Hospital and
Research Centre, Bagalkot, Karnataka, India
3Department of Pathology, SRL Diagnostics, Bangalore,
Karnataka, India
*Corresponding author: Vishwas D Pai, Department of
Surgical Oncology, Kerudi Cancer Hospital and Research
Centre, Bagalkot 587101, Karnataka, India, Tel: +91-
9449333502; E-mail:
Received: October 28, 2015 | Published: December 29,
2015
Submit Manuscript | http://medcraveonline.com Gastroenterol Hepatol Open Access 2015, 3(2): 00080
Abbreviations: CECT: Contrast Enhanced Computed
Tomography; MRI: Magnetic Resonance Imaging; CT: Computed
Tomography
Introduction
Schwannomas are the most common types of peripheral nerve
neoplasms arising from the Schwann cells of the neural sheath.
Although they may occur in any part of the body, only 6% are
          
estimate since majority of these remain asymptomatic. Because
of the location, these tumors can grow to very large size before

because of the narrow working space available and proximity to
the vital structures including external iliac vessels as well as the
ureter. In addition, abundant vascularity of the presacral plexus of
  
the type of the tumor on preoperative imaging studies is essential
to determine the appropriate approach for these rare tumors. We
are presenting a case of presacral schwannoma resected via an
open, intraperitoneal approach.
Case Report
A 40 year old gentleman presented with pain in the lower
abdomen of 1 year duration. On evaluation with contrast
enhanced computed tomography of abdomen (CECT), a soft
tissue mass of size 10 x 8 x 6 cm was detected in the presacral

it as dumb-bell shaped tumor with no intra spinal extension
representing a nerve sheath tumour (Figure 1a). Intra operatively,

right external iliac artery and vein. Tumor was then separated
from the sacrum by sharp and blunt dissection. Excision of the
tumor was completed after clipping the 5th lumbar nerve root
on the right side (Figure 1b). Duration of the surgery was 100
minutes and there was 100 ml of blood loss. Post operative course
was uneventful and he was discharged on 4th post operative day.

as a benign schwannoma (Figure 1c).
Discussion
Presacral schwannomas are rare accounting for 1-5% of
spinal schwannomas [2-4]. Less than 30 cases of presacral
schwannoma have been reported in English literature [5]. Klimo

     
sacrum but erode the wall of the sacrum and extend into the
adjacent spaces. Type 3 tumors are located predominantly in the
presacral or retro peritoneal area [6].
Most of these tumors remain asymptomatic and are detected
      
symptoms. Because of their slow growing nature and their
location in the presacral fossa they can reach very large size while
being asymptomatic and can even erode the sacrum. MRI is more

the tumor as well as its relationship with surrounding structures
including intra spinous extension [7].
Complete surgical resection remains the treatment of choice.
In general, posterior approach is preferable for type 1 tumors;
anterior approach is preferable for type 3 tumors and combined
anterior and posterior approach is preferable for type 2 tumors
[8]. Anterior approach may be either trans peritoneal or extra
peritoneal. Majority of the previous reports have reported trans
peritoneal approach although extra peritoneal approach has also
been reported by few authors [9,10]. The present patient had type
3 tumor and hence was resected via anterior trans peritoneal
approach.
Case Report
Abstract
Presacral tumors are rare. Neurogenic tumors in this area are even rarer with
only case report and short case series being reported in literature. Most of
these tumors remain asymptomatic till they reach size large enough to cause
pressure symptoms. Magnetic resonance imaging (MRI) of the pelvis is the
most preferred imaging modality for preoperative diagnosis as well treatment
planning. Complete surgical resection is the treatment of choice. Approach to
surgical resection depends on the type of the tumour. After complete excision
of the tumor, recurrence is rare. Up to 10-50% recurrence has been reported in
literature after incomplete resections. Adjuvant treatment is not recommended
even in incomplete resections or recurrences. We are presenting a case of type
3 presacral schwannoma resected by open, anterior, trans peritoneal approach.
Keywords: Presacral schwannoma; Neurogenic tumors; Anterior transperitoneal
approach
Presacral Schwannoma Resected Via Anterior Trans Peritoneal Approach: A Case Report 2/2
Copyright:
©2015 Pai et al.
Citation: Pai VD, Pawale A, Ravindranath S (2015) Presacral Schwannoma Resected Via Anterior Trans Peritoneal Approach: A Case Report. Gastroenterol
Hepatol Open Access 3(2): 00080. DOI: 10.15406/ghoa.2015.03.00080
Figure 1A: MRI pelvis, axial section showing soft tissue mass arising in the presacral area with no obvious
intra spinous extension.
Figure 1B: Gross picture of specimen of the presacral tumor resected.
Figure 1C: Spindle cell tumor with indented wavy nuclei revealing focal palisade.
Conclusion
Presacral schwannoma are rare nerve sheath tumors. MRI is
the most preferred imaging modality. Complete surgical resection
can be performed safely via anterior transabdominal approach.
References
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(2002) Sacral schwannoma: case report. Turk Neuro chir 12: 247-505.
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Giant intrasacral schwannomas: report of six cases. Acta Neurochir
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M, et al. (2005) Laparoscopic resection of presacral schwannomas.
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6. Klimo P, Rao G, Schmidt RH, Schmidt MH (2003) Nerve sheath
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Neurosurg Focus 15(2): E12.
7. Popuri R, Davies AM (2002) MR imaging features of giant pre-sacral
schwannomas: a report of four cases. Eur Radiol 12(9): 2365-2369.
8. Mazreku A, Karaj A, Avdia I, Bilali S (2010) The presentation and
management of presacral tumors. Acta Chir Iugosl 57(2): 55-59.
9. Rousseau MA, Pascal-Mousselard H, Lazennec JY, Saillant G (2005) The
mini-invasive anterior extra peritoneal approach to the pelvis. Eur J
Surg Oncol 31(8): 924-926.
10. Senoglu M, Bulbuloglu E, Demirpolat G, Altun I, Ciralik H (2010)
The anterior extraperitoneal approach to the rare presacral/
retroperitoneal schwannoma. Bratisl Lek Listy 111(10): 558-561.
ResearchGate has not been able to resolve any citations for this publication.
Article
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Presacral/retroperitoneal schwannomas are extremely unusual and their surgical approach is challenging. Various surgical approaches have been proposed. Here we describe our experience with the anterior extraperitoneal approach for the Type 3 presacral/retroperitoneal schwannoma. A 33-year-old woman presented with a history of infertility and a presacral/retroperitoneal mass. The patient underwent abdominal/pelvic CT and MRI that demonstrated presence of a solid, well circumscribed Type 3 presacral/retroperitoneal schwannoma. The anterior extraperitoneal approach was successfully used to remove the presacral/retroperitoneal schwannoma. The histopathological evaluation confirmed the preoperative diagnosis. The anterior extraperitoneal approach is helpful as an alternative approach in the surgical management of benign Type 3 presacral/retroperitoneal schwannomas (Fig. 4, Ref. 15).
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Nerve sheath tumors that involve the sacrum are rare. Delayed presentation is common because of their slow-growing nature, the permissive surrounding anatomical environment, and nonspecific symptoms. Consequently, these tumors are usually of considerable size at the time of diagnosis. The authors discuss a case of a sacral nerve sheath tumor. They also propose a classification scheme for these tumors based on their location with respect to the sacrum into three types (Types I–III). Type I tumors are confined to the sacrum; Type II originate within the sacrum but then locally metastasize through the anterior and posterior sacral walls into the presacral and subcutaneous spaces, respectively; and Type III are located primarily in the presacral/retroperitoneal area. The overwhelming majority of sacral nerve sheath tumors are schwannomas. Neurofibromas and malignant nerve sheath tumors are exceedingly rare. Regardless of their histological features, the goal of treatment is complete excision. Adjuvant radiotherapy may be used in patients in whom resection was subtotal. Approaches to the sacrum can generally be classified as anterior or posterior. Type I tumors may be resected via a posterior approach alone, Type III may require an anterior approach, and Type II tumors usually require combined anterior–posterior surgery.
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Presacral tumors are particularly rare in the adult. Schwannomas are neurogenic neoplasms, rarely occurring in the retroperitoneum and the pelvis. Presented herein are the cases of 2 female patients with chronic pelvic pain who were discovered to have presacral schwannomas and were managed laparoscopically. Laparoscopy is a safe and efficient option in approaching benign pelvic tumors and might offer the advantage of better visualization of structures due to the magnification of laparoscopic view, especially in narrow anatomic spaces.
Sacral schwannoma: case report
  • Z Karabulut
  • H Besim
  • E O Hamamcı
  • S Bostanoğlu
  • N Erverdi
Karabulut Z, Besim H, Hamamcı EO, Bostanoğlu S, Erverdi N, et al. (2002) Sacral schwannoma: case report. Turk Neuro chir 12: 247-505.