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Autoimmune pancreatitis and IgG4-related systemic diseases

Autoimmune pancreatitis (AIP) is a rare form of chronic pancreatitis that is characterized by lymphoplasmacytic infiltrate, storiform fibrosis, obliterative phlebitis, and increased IgG4(+) plasma cells. Serum IgG4 levels usually are elevated. Patients with AIP frequently have disease affecting othe...

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Detaylı Bibliyografya
Asıl Yazarlar: Zhang, Lizhi, Smyrk, Thomas C
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: e-Century Publishing Corporation 2010
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2897107/
https://ncbi.nlm.nih.gov/pubmed/20606730
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