Ana-Belen Larque’s research while affiliated with Hospital Clínic de Barcelona and other places

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Publications (4)


Figure 1 Knee radiograph and knee CT of Patient #1 showing radiological findings suggestive of prosthetic infection. (A) An AP knee radiograph depicting a unicompartmental prosthesis located in the medial compartment of the knee, revealing an area of osteolysis adjacent to the tibial component (arrow). (B) A knee CT scan in bone reconstruction and coronal plane confirming the observed area of osteolysis in the X-ray (arrow). (C,D) Knee CT in soft tissue reconstruction, presented in axial sections, illustrating abundant joint effusion with synovitis (*) and the presence of a PLN (circle). This PLN exhibits signs of infection, characterized by a rounded morphology, an absent fatty hilum, and imprecise margins with slight adjacent fat trabeculation. CT, computed tomography; AP, anteroposterior; PLN, popliteal lymphadenopathy.
Figure 4 Progressive lateral knee radiographs of Patient #3 performed annually to evaluate prosthetic loosening demonstrate an increase in the density of the popliteal recess each year (arrows), corresponding to the migration of cement to the popliteal recess. No PLNs are observable in the radiographs. Images (A) and (B) serve as controls to evaluate prosthetic loosening, while (C) has already undergone prosthetic replacement. PLN, popliteal lymphadenopathy.
Increased cortical density in popliteal lymphadenopathy as a promising radiological sign to help differentiate adverse local tissue reaction from infections in complications following a knee arthroplasty—three case reports
  • Article
  • Full-text available

November 2024

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9 Reads

Quantitative Imaging in Medicine and Surgery

Marta Porta-Vilaró

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Ana-Belen Larque

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Background Total knee arthroplasty (TKA) is an effective surgical procedure for managing advanced osteoarthritis of the knee, significantly reducing pain and improving function. However, some patients experience complications leading to revision surgery, often caused by periprosthetic joint infection (PJI) in early failures and adverse local tissue reactions (ALTR) or aseptic loosening in late failures. Differentiating between PJI and ALTR is crucial because their clinical presentations can overlap, yet their treatments are distinct. While traditional imaging like radiography is useful for assessing alignment and detecting osteolysis, it may miss subtle pathological changes. Computed tomography (CT) has been increasingly utilized to provide additional diagnostic detail, especially regarding lymphadenopathy, which has been linked to septic complications in hip prostheses. However, the role of popliteal lymphadenopathy (PLN) in knee prosthesis complications remains unexplored. Case Description We present three cases of knee prosthesis complications, diagnosed as either septic or aseptic, where CT imaging revealed distinct patterns of PLN. In the first case, which involved septic loosening, three enlarged PLNs with rounded morphology, normal density, and an absent fatty hilum were observed. The second case, complicated by ALTR and a periprosthetic fracture, showed six PLNs with increased cortical density but a preserved fatty hilum. The third and final case of aseptic loosening revealed three PLNs with increased cortical density and prosthetic debris in the popliteal recess. These findings suggest a range of PLN characteristics depending on the underlying complication, with distinct differences in morphology and cortical density observed between septic and aseptic cases. Conclusions The presence and characteristics of PLN may serve as a valuable imaging biomarker for diagnosing and differentiating knee prosthesis complications. CT evaluation of PLNs could enhance diagnostic accuracy, particularly in distinguishing between PJI and ALTR, prompting further research to validate these findings and explore their diagnostic potential.

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Figure 1 Initial presentation of each case (#1, #2, #3, #4). Fibrogastroscopy (A) revealing an ulcerated, irregular, friable, infiltrative lesion involving the prepyloric region of the antrum and deforming the pylorus in Patient #1 (arrow), an extensive ulcerated lesion on the anterior aspect and greater curvature of the gastric body in Patient #2 (arrow), a protruding lesion on the posterior aspect and lesser curvature of the distal antrum in Patient #3 (arrow) and a deep ulcer on the greater curvature at the mid-body level, characterized by irregular edges and retraction in Patient #4 (arrow). Thoracoabdominal CT in axial plane and soft tissue reconstruction (B) showing thickening of the stomach walls in the antropyloric region (arrow), with small locoregional lymph nodes (*) in Patient #1. Patient #2 exhibited parietal thickening of the greater gastric curvature (white arrow) and a lymph node in the gastrohepatic ligament (*). In patient #3, wall thickening was observed at the antrum (arrow), while Patient #4 showed no signs of local or distant extension. (C) Thoracoabdominal CT in coronal plane and bone reconstruction revealed no evidence of bone metastases in any of the patients. CT, computed tomography.
Figure 7 Progression in the form of multiple osteoblastic BM was observed in periodic CT scans, involving the spine and pelvis in Patient #1 (arrows), and affecting the sternum, scapulae, and ribs in Patients #2 and #3. Patient #4 presents a pattern of endomedullary metastasis with diffuse involvement of the entire skeletal framework. BM, bone metastasis; CT, computed tomography.
Metastatic bone lesion type in gastric cancer patients: imaging findings of case reports

November 2024

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6 Reads

Quantitative Imaging in Medicine and Surgery

Background Gastric cancer (GC) is the fifth most common cancer globally and the third leading cause of cancer-related deaths. While it predominantly metastasizes to the liver, peritoneum, and lungs, bone metastasis (BM) is a rare but severe complication. BM occurs in 1–20% of GC cases and is associated with a poor prognosis. Typically, BM in GC presents at advanced stages, often with non-specific symptoms, making early detection challenging. Case Description This retrospective study analyzed 118 GC patients treated at our institution from 2010 to 2020. Among them, eight patients (6.8%) developed BM, with an equal split between osteoblastic and osteolytic types. Osteoblastic BM was observed exclusively in men, with a mean age of 72.25 years. The median time from GC diagnosis to BM onset was 27.5 months. BM was primarily detected through periodic thoracoabdominal CT scans, and bone scintigraphy confirmed the osteoblastic nature of the lesions. All patients had advanced GC and were under palliative care at the time of BM diagnosis. The average survival time from BM diagnosis was 8.5 months. Conclusions BM in GC patients is rare but significantly worsens the prognosis. The findings suggest that osteoblastic BM may be more common in GC than previously reported, potentially due to improved imaging techniques and extended patient survival. This study underscores the importance of vigilant radiological monitoring in GC patients, particularly those with non-specific symptoms suggestive of BM. Enhanced collaboration between oncology and palliative care teams is essential to manage symptoms effectively and improve patient quality of life. Future research should focus on the incidence and management of BM in GC, particularly the role of targeted therapies in improving patient quality of life. Keywords Bone metastasis (BM); gastric cancer (GC); osteoblastic; disease progression; case report


Corrigendum: Ex vivo normothermic preservation of a kidney graft from uncontrolled donation after circulatory death over 73 hours

March 2024

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28 Reads

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1 Citation


Hemodynamic and biochemical analyses during kidney perfusion. (A) Mean perfusion pressure. (B) Flow rate during perfusion. (C) Renal resistance index (RRI) during perfusion. (D) Perfusate hemoglobin during perfusion. The black arrows represent red blood cell transfusions. (E) Perfusate pH during kidney perfusion. (F) Perfusate sodium during perfusion. (G) Perfusate potassium during perfusion. (H) Lactate levels during perfusion. (I) Kidney urine output.
Macro- and microscopical assessment of the kidney graft during perfusion. (A) Macroscopical assessment before perfusion onset (time 0). (B) Macroscopical assessment at 24 h of perfusion. (C) Macroscopical assessment at 48 h of perfusion. (D) Macroscopical assessment at 73 h of perfusion. (E) H&E staining of a kidney biopsy at time 0 (optical microscope, ×20). (F) H&E staining of a kidney biopsy at 24 h (optical microscope, ×20). (G) H&E staining of a kidney biopsy at 48 h (optical microscope, ×20). (H) H&E staining of a kidney biopsy at 72 h (optical microscope, ×20). H&E, hematoxylin–eosin.
(A) Real-time qPCR analysis for KIM-1 expression. (B) Real-time qPCR analysis for TGFβ expression. (C) Real-time qPCR analysis for VEGF expression. (D) Real-time qPCR analysis for TIMP1 expression. (E) Real-time qPCR analysis for β-catenin expression. (F) Real-time qPCR analysis for Ki67 expression.
Ex vivo normothermic preservation of a kidney graft from uncontrolled donation after circulatory death over 73 hours

January 2024

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61 Reads

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2 Citations

The transplant community is focused on prolonging the ex vivo preservation time of kidney grafts to allow for long-distance kidney graft transportation, assess the viability of marginal grafts, and optimize a platform for the translation of innovative therapeutics to clinical practice, especially those focused on cell and vector delivery to organ conditioning and reprogramming. We describe the first case of feasible preservation of a kidney from a donor after uncontrolled circulatory death over a 73-h period using normothermic perfusion and analyze hemodynamic, biochemical, histological, and transcriptomic parameters for inflammation and kidney injury. The mean pressure and flow values were 71.24 ± 9.62 mmHg and 99.65 ± 18.54 mL/min, respectively. The temperature range was 36.7°C–37.2°C. The renal resistance index was 0.75 ± 0.15 mmHg/mL/min. The mean pH was 7.29 ± 0.15. The lactate concentration peak increased until 213 mg/dL at 6 h, reaching normal values after 34 h of perfusion (8.92 mg/dL). The total urine output at the end of perfusion was 1.185 mL. Histological analysis revealed no significant increase in acute tubular necrosis (ATN) severity as perfusion progressed. The expression of KIM-1, VEGF, and TGFβ decreased after 6–18 h of perfusion until 60 h in which the expression of these genes increased again together with the expression of β-catenin, Ki67, and TIMP1. We show that normothermic perfusion can maintain a kidney graft viable ex vivo for 3 days, thus allowing a rapid translation of pre-clinical therapeutics to clinical practice.

Citations (2)


... And finally, in a recent trial by OrganOx Ltd., the first evidence of prolongation of total preservation times using NMP technology exists, potentially impacting clinical practice as priorly seen in liver transplantation [37]. Preclinical data suggest that prolonged kidney preservation through NMP might be feasible within the next years: 73 h of NMP have been reported-the longest experimentally perfused kidney grafts to date [98]. Multiple benefits of extended kidney NMP exist: organ storage under preserved metabolism, improved reconditioning, use as a platform for novel therapeutics, and potentially organ regeneration can be facilitated with the application of this technology [99,100]. ...

Reference:

Normothermic Machine Perfusion of Kidney Grafts: Devices, Endpoints, and Clinical Implementation
Corrigendum: Ex vivo normothermic preservation of a kidney graft from uncontrolled donation after circulatory death over 73 hours

... Perfusion parameters like hemoglobin concentration, oxygen saturation, temperature, flow, pressure, renal resistance index, and urine production are tracked throughout perfusion. Using a historical control group of SCS kidneys, their chosen primary endpoint is defined as adverse events, while DGF, PNF, graft renal function, patient and graft survival, and others are considered secondary endpoints [39,40]. Using an uncontrolled DCD graft, this device was able to preserve its viability for 73 h [40]. ...

Ex vivo normothermic preservation of a kidney graft from uncontrolled donation after circulatory death over 73 hours