Literature DB >> 16773691

Sclerosing cholecystitis associated with autoimmune pancreatitis.

Terumi Kamisawa1, Yuyang Tu, Hitoshi Nakajima, Naoto Egawa, Kouji Tsuruta, Atsutake Okamoto, Shinichirou Horiguchi.   

Abstract

AIM: To evaluate the histopathological and radiological findings of the gallbladder in patients with autoimmune pancreatitis (AIP).
METHODS: The radiological findings of the gallbladder of 19 AIP patients were retrospectively reviewed. Resected gallbladders of 8 AIP patients were examined histologically and were immunostained with anti-IgG4 antibody. Controls consisted of gallbladders resected for symptomatic gallstones (n = 10) and those removed during pancreatoduodenectomy for pancreatic carcinoma (n = 10), as well as extrahepatic bile ducts and pancreases removed by pancreatoduodenectomy for pancreatic carcinoma (n = 10).
RESULTS: Thickening of the gallbladder wall was detected by ultrasound and/or computed tomography in 10 patients with AIP (3 severe and 7 moderate); in these patients severe stenosis of the extrahepatic bile duct was also noted. Histologically, thickening of the gallbladder was detected in 6 of 8 (75%) patients with AIP; 4 cases had transmural lymphoplasmacytic infiltration with fibrosis, and 2 cases had mucosal-based lymphoplasmacytic infiltration. Considerable transmural thickening of the extrahepatic bile duct wall with dense fibrosis and diffuse lymphoplasmacytic infiltration was detected in 7 patients. Immunohistochemically, severe or moderate infiltration of IgG4-positive plasma cells was detected in the gallbladder, bile duct, and pancreas of all 8 patients, but was not detected in controls.
CONCLUSION: Gallbladder wall thickening with fibrosis and abundant infiltration of IgG4-positive plasma cells is frequently detected in patients with AIP. We propose the use of a new term, sclerosing cholecystitis, for these cases that are induced by the same mechanism as sclerosing pancreatitis or sclerosing cholangitis in AIP.

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Year:  2006        PMID: 16773691      PMCID: PMC4087467          DOI: 10.3748/wjg.v12.i23.3736

Source DB:  PubMed          Journal:  World J Gastroenterol        ISSN: 1007-9327            Impact factor:   5.742


  10 in total

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2.  Close relationship between autoimmune pancreatitis and multifocal fibrosclerosis.

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3.  Clinical differences between primary sclerosing cholangitis and sclerosing cholangitis with autoimmune pancreatitis.

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4.  ERCP features in 27 patients with autoimmune pancreatitis.

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5.  Clinical difficulties in the differentiation of autoimmune pancreatitis and pancreatic carcinoma.

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6.  Involvement of the biliary system in autoimmune pancreatitis: a follow-up study.

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8.  A new clinicopathological entity of IgG4-related autoimmune disease.

Authors:  Terumi Kamisawa; Nobuaki Funata; Yukiko Hayashi; Yoshinobu Eishi; Morio Koike; Kouji Tsuruta; Atsutake Okamoto; Naoto Egawa; Hitoshi Nakajima
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9.  Lymphoplasmacytic chronic cholecystitis and biliary tract disease in patients with lymphoplasmacytic sclerosing pancreatitis.

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  10 in total
  13 in total

1.  Comparison of sclerosing cholangitis with autoimmune pancreatitis and infiltrative extrahepatic cholangiocarcinoma: multidetector-row computed tomography findings.

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6.  IgG4-associated cholecystitis: another clue in the diagnosis of autoimmune pancreatitis.

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Review 8.  IgG4-related sclerosing disease.

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Review 9.  B-mode ultrasonographic diagnosis in gallbladder wall thickening.

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10.  Differentiating immunoglobulin g4-related sclerosing cholangitis from hilar cholangiocarcinoma.

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