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Immunoglobulin G4‐related disease mimicking gallbladder cancer with associated choledochal cyst: A case report of a malignant masquerade
Immunoglobulin G4 (IgG4)‐related disease is a recently described autoimmune disease that can involve diverse organ systems, causing pancreatitis, cholangitis, retroperitoneal fibrosis, and thyroiditis to name a few. Key histological features include storiform fibrosis, obliterative venulitis, and in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Publishing Asia Pty Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891023/ https://www.ncbi.nlm.nih.gov/pubmed/31832557 http://dx.doi.org/10.1002/jgh3.12154 |
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author | Kulkarni, Aditya A Soni, Praveen Sharma, Vipan K Bal, Amanjit Rana, Surinder S Gupta, Rajesh |
author_facet | Kulkarni, Aditya A Soni, Praveen Sharma, Vipan K Bal, Amanjit Rana, Surinder S Gupta, Rajesh |
author_sort | Kulkarni, Aditya A |
collection | PubMed |
description | Immunoglobulin G4 (IgG4)‐related disease is a recently described autoimmune disease that can involve diverse organ systems, causing pancreatitis, cholangitis, retroperitoneal fibrosis, and thyroiditis to name a few. Key histological features include storiform fibrosis, obliterative venulitis, and intense inflammatory infiltrate composed of lymphoplasmacytic cells. The disease has a tendency to present with mass‐forming lesions, often difficult to differentiate from malignant processes. We report the case of a 48‐year‐old male from an area endemic for gallbladder cancer (north India). He presented with a short history of abdominal pain and was found to have asymmetric thickening of the gallbladder wall with a soft‐tissue mass invading the adjacent liver. In addition, the bile duct was dilated throughout its extent. A clinical and radiological diagnosis of gallbladder cancer with choledochal cyst was made, and the patient underwent radical cholecystectomy with bile duct excision. Histopathology surprisingly demonstrated IgG4‐related disease with no evidence of malignancy. Notably, serum levels of immunoglobulins were found to be normal. Preoperative diagnosis was challenging due to the absence of other manifestations. IgG4‐related disease is a possible diagnostic pitfall and should be included as a possible differential diagnosis for gallbladder masses. |
format | Online Article Text |
id | pubmed-6891023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wiley Publishing Asia Pty Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-68910232019-12-12 Immunoglobulin G4‐related disease mimicking gallbladder cancer with associated choledochal cyst: A case report of a malignant masquerade Kulkarni, Aditya A Soni, Praveen Sharma, Vipan K Bal, Amanjit Rana, Surinder S Gupta, Rajesh JGH Open Case Reports Immunoglobulin G4 (IgG4)‐related disease is a recently described autoimmune disease that can involve diverse organ systems, causing pancreatitis, cholangitis, retroperitoneal fibrosis, and thyroiditis to name a few. Key histological features include storiform fibrosis, obliterative venulitis, and intense inflammatory infiltrate composed of lymphoplasmacytic cells. The disease has a tendency to present with mass‐forming lesions, often difficult to differentiate from malignant processes. We report the case of a 48‐year‐old male from an area endemic for gallbladder cancer (north India). He presented with a short history of abdominal pain and was found to have asymmetric thickening of the gallbladder wall with a soft‐tissue mass invading the adjacent liver. In addition, the bile duct was dilated throughout its extent. A clinical and radiological diagnosis of gallbladder cancer with choledochal cyst was made, and the patient underwent radical cholecystectomy with bile duct excision. Histopathology surprisingly demonstrated IgG4‐related disease with no evidence of malignancy. Notably, serum levels of immunoglobulins were found to be normal. Preoperative diagnosis was challenging due to the absence of other manifestations. IgG4‐related disease is a possible diagnostic pitfall and should be included as a possible differential diagnosis for gallbladder masses. Wiley Publishing Asia Pty Ltd 2019-02-22 /pmc/articles/PMC6891023/ /pubmed/31832557 http://dx.doi.org/10.1002/jgh3.12154 Text en © 2019 The Authors. JGH Open: An open access journal of gastroenterology and hepatology published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Case Reports Kulkarni, Aditya A Soni, Praveen Sharma, Vipan K Bal, Amanjit Rana, Surinder S Gupta, Rajesh Immunoglobulin G4‐related disease mimicking gallbladder cancer with associated choledochal cyst: A case report of a malignant masquerade |
title | Immunoglobulin G4‐related disease mimicking gallbladder cancer with associated choledochal cyst: A case report of a malignant masquerade |
title_full | Immunoglobulin G4‐related disease mimicking gallbladder cancer with associated choledochal cyst: A case report of a malignant masquerade |
title_fullStr | Immunoglobulin G4‐related disease mimicking gallbladder cancer with associated choledochal cyst: A case report of a malignant masquerade |
title_full_unstemmed | Immunoglobulin G4‐related disease mimicking gallbladder cancer with associated choledochal cyst: A case report of a malignant masquerade |
title_short | Immunoglobulin G4‐related disease mimicking gallbladder cancer with associated choledochal cyst: A case report of a malignant masquerade |
title_sort | immunoglobulin g4‐related disease mimicking gallbladder cancer with associated choledochal cyst: a case report of a malignant masquerade |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891023/ https://www.ncbi.nlm.nih.gov/pubmed/31832557 http://dx.doi.org/10.1002/jgh3.12154 |
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