Literature DB >> 20157837

A case of incidentally detected IgG4-related sclerosing disease involving inflammatory abdominal aortic aneurysm and autoimmune pancreatitis.

Yasunori Matsuki1, Kimiya Sato, Akira Fujikawa, Yukishige Kyoto, Hiroshi Hashimoto, Yukiya Hakozaki.   

Abstract

A 59-year-old asymptomatic man was incidentally found to have a periaortic mass and an elevated serum amylase level during his medical check-up. Additional findings, such as infiltration of immunoglobulin G4 (IgG4)-producing plasma cells in the mass lesion, elevation of serum IgG4 (1000 mg/dl), and pancreatic duct narrowing as evidenced on a magnetic resonance cholangiopancreatography scan, confirmed the diagnosis as retroperitoneal fibrosis complicated with autoimmune pancreatitis. The patient responded favorably to steroid treatment before the appearance of symptoms.

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Year:  2010        PMID: 20157837     DOI: 10.1007/s10165-010-0272-z

Source DB:  PubMed          Journal:  Mod Rheumatol        ISSN: 1439-7595            Impact factor:   3.023


  2 in total

1.  IgG4-related Inflammatory Abdominal Aortic Aneurysm, Spectrum of IgG4-related Chronic Periaortitis.

Authors:  Satomi Kasashima; Yoh Zen
Journal:  Ann Vasc Dis       Date:  2010-12-02

2.  An aortoduodenal fistula as a complication of immunoglobulin G4-related disease.

Authors:  Momir Sarac; Ivan Marjanovic; Mihailo Bezmarevic; Uros Zoranovic; Stanko Petrovic; Miodrag Mihajlovic
Journal:  World J Gastroenterol       Date:  2012-11-14       Impact factor: 5.742

  2 in total

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