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Case Reports
. 2022 May-Jun;12(3):1012-1016.
doi: 10.1016/j.jceh.2021.11.001. Epub 2021 Nov 16.

IgG4-Related Sclerosing Cholangitis with Cholecystitis Mimicking Cholangiocarcinoma: A Case Report

Affiliations
Case Reports

IgG4-Related Sclerosing Cholangitis with Cholecystitis Mimicking Cholangiocarcinoma: A Case Report

Babu L Meena et al. J Clin Exp Hepatol. 2022 May-Jun.

Abstract

IgG4-related diseases are rare multisystem disorders involving salivary glands, retroperitoneum, pancreas, biliary tract, and liver. Isolated biliary strictures and gall bladder involvement are rare in such patients, and presentation with cholangitis and weight loss can misguide the diagnosis toward malignancy. Here, we report an interesting case of IgG4-related biliary stricture with gall bladder involvement, presented with cholangitis and weight loss. The initial symptoms and imaging were guided toward the malignant possibilities of cholangiocarcinoma and pancreatic carcinoma. However, endosonography, serology, and histopathology clinched the diagnosis of IgG4-related disease. The patient was managed without any biliary intervention and with antibiotics, steroids, and steroid-sparing agents. There was a relapse of disease during the steroids taper that improved after hiking its doses. The disease responded with medical management on follow-up. We demonstrated the effectiveness of steroid-sparing agents to treat IgG4-related diseases, especially to avert the steroid-related adverse effects. This case highlights the possible mislead for the diagnosis and delayed management of IgG4 disease due to shared clinical features with hepatobiliary malignancies and the effectiveness of noninvasive measures of management.

Keywords: AIP, Autoimmune pancreatitis; ANA, Antinuclear antibody; CA 19-9, Carbohydrate antigen 19-9; CT, Computed tomography; EUS, endoscopic ultrasound; FNAC, Fine needle aspiration cytology; HISTORt, Histology, Imaging, Serology, treatment response, relapse; HOP, Head of pancreas; HPF, High power field; IgG4 cholangitis; IgG4 cholecystitis; IgG4 disease; IgG4HBD, IgG4-related hepatobiliary disease; IgG4RD, IgG4-related disease; IgG4SC, IgG4 sclerosing cholangitis; MRCP, magnetic resonance cholangiopancreatography; PSC, Primary sclerosing cholangitis; RF, Rheumatoid factor; RNA, Ribonucleic acid; cholangiocarcinoma; periampullary carcinoma.

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Figures

Figure 1
Figure 1
a: MRCP image showing central and peripheral IHBRD, dilated CBD (14 mm), with abrupt cutoff and stricture at the distal end. b: Endoscopic ultrasound showing diffuse symmetrical mural thickening of the wall of gall bladder with a pericholecystic halo. c: Ampullary Biopsy- IgG4 immunostain, low power view shows diffuse positivity of the plasma cells (>10/hpf), few IgG4 negative plasma cells also seen. d: Repeat MRCP at six months of immunosuppression; MRCP image shows mildly prominent CBD 8 mm and minimal central IHBRD with smooth tapering of the distal end. e: Repeat EUS at six months of immunosuppression shows resolution of gall bladder wall thickening.

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