Internal Medicine
Online ISSN : 1349-7235
Print ISSN : 0918-2918
ISSN-L : 0918-2918
CASE REPORTS
Two Siblings with Type 1 Autoimmune Pancreatitis
Takayuki WatanabeMasahiro MaruyamaTetsuya ItoKeita KanaiTakaya OguchiTakashi MurakiHideaki HamanoNorikazu ArakuraMasao OtaShigeyuki Kawa
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2013 Volume 52 Issue 8 Pages 895-899

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Abstract

Type 1 autoimmune pancreatitis (AIP) is characterized by a high serum IgG4 concentration and is closely associated with the HLA-DRB1*04:05-DQB1*04:01 haplotype, for which family studies may disclose its immunogenetic significance. In the present study, we encountered two male siblings with type 1 AIP who exhibited diffuse pancreatic swelling with a capsule-like rim and diffuse pancreatic duct stricture. The younger brother also displayed characteristic IgG4-related sialadenitis and retroperitoneal fibrosis. Contrary to our expectations, the siblings showed only normal or slightly elevated values of serum IgG4 and no HLA DRB1*04:05-DQB1*04:01 haplotype, suggesting that type 1 autoimmune pancreatitis is associated with multiple immunogenetic factors.

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© 2013 by The Japanese Society of Internal Medicine
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