A Case of Autoimmune Pancreatitis Diagnosed by Immunohistochemical Staining of IgG4 / 대한소화기내시경학회지
Korean Journal of Gastrointestinal Endoscopy
; : 205-209, 2007.
Article
in Korean
| WPRIM (Western Pacific)
| ID: wpr-147160
Responsible library:
WPRO
ABSTRACT
Autoimmune pancreatitis is a distinct entity with characteristic morphological, histological and clinical features. Since the first report in 1961, there have been many reports on autoantibodies associated with autoimmune pancreatitis. Lymphoplasmacytic infiltration with fibrosis is the characteristic histological feature of autoimmune pancreatitis. Elevation of immunoglobulin G4 (IgG4), a subtype of IgG, can be seen in autoimmune pancreatitis. A few reports of autoimmune pancreatitis based on immunostaining of IgG4 have been published, but no reports have been published in Korea. We present here the first report of autoimmune pancreatitis, based on an increased serum IgG4 level and plasma cell infiltration that showed IgG4 positivity by immunohistochemical staining of the major papilla.
Full text:
Available
Database:
WPRIM (Western Pacific)
Main subject:
Pancreatitis
/
Plasma Cells
/
Autoantibodies
/
Fibrosis
/
Immunoglobulin G
/
Immunoglobulins
/
Korea
Type of study:
Diagnostic study
Country/Region as subject:
Asia
Language:
Korean
Journal:
Korean Journal of Gastrointestinal Endoscopy
Year:
2007
Document type:
Article