Unusual Multiorgan Immunoglobulin G4 (IgG4) Inflammation: Autoimmune Pancreatitis, Mikulicz Syndrome, and IgG4 Mastitis

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F13%3A00069408" target="_blank" >RIV/00216224:14110/13:00069408 - isvavai.cz</a>
Alternative codes found
RIV/61988987:17110/13:A140194P RIV/65269705:_____/13:#0002070 RIV/00159816:_____/13:00060700 RIV/00216208:11140/13:10296044
Result on the web
<a href="http://dx.doi.org/10.5009/gnl.2013.7.5.621" target="_blank" >http://dx.doi.org/10.5009/gnl.2013.7.5.621</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.5009/gnl.2013.7.5.621" target="_blank" >10.5009/gnl.2013.7.5.621</a>

Result language
angličtina
Original language name
Unusual Multiorgan Immunoglobulin G4 (IgG4) Inflammation: Autoimmune Pancreatitis, Mikulicz Syndrome, and IgG4 Mastitis
Original language description
Autoimmune pancreatitis (AIP) type 1 is commonly associated with simultaneous involvement of extrapancreatic organs. We describe a case report of a 58-year-old female with findings of AIP (according to Asian criteria), IgG4-positive mastitis, and histologically verified Mikulicz syndrome. The effect of corticoid therapy supported the diagnosis of AIP and simultaneously led to the eradication of recurrent mastitis. Our case report supports the concept of systemic IgG4 syndrome with multisystem involvement.
Czech name
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Czech description
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Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FE - Other fields of internal medicine
OECD FORD branch
—

Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2013
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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