Internal Medicine
Online ISSN : 1349-7235
Print ISSN : 0918-2918
ISSN-L : 0918-2918
CASE REPORTS
Autoimmune Pancreatitis with Histologically Proven Lymphoplasmacytic Sclerosing Pancreatitis with Granulocytic Epithelial Lesions
Tsukasa IkeuraMakoto TakaokaKazushige UchidaMasaaki ShimataniHideaki MiyoshiTakeo KusudaAkiko KurishimaYuri FukuiKimi SumimotoSohei SatoiChisato OheYoshiko UemuraA-Hon KwonKazuichi Okazaki
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ジャーナル オープンアクセス

2012 年 51 巻 7 号 p. 733-737

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Recent histological and clinical studies have suggested the existence of 2 distinct types of autoimmune pancreatitis (AIP): type 1 AIP related to IgG4, exhibiting lymphoplasmacytic sclerosing pancreatitis (LPSP), and type 2 AIP related to granulocyte epithelial lesions (GELs), exhibiting idiopathic duct-centric chronic pancreatitis (IDCP). We herein present a case of type 1 AIP with histologically proven LPSP with GELs. This patient had neither serum IgG4 elevation nor MPD narrowing. In this case, the clinically and histologically atypical findings for type 1 AIP are intriguing.
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© 2012 by The Japanese Society of Internal Medicine
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