IgG4-related Diseases – A Rare Polycystic Form of Ormond’s Disease
Currently, Ormond’s disease is classified among IgG4-associated diseases. Its clinical manifestation varies and is characterized by the presence of fibrous retroperitoneal tissue that often affects the ureters or abdominal aorta and iliac arteries. We present a unique case of the polycystic form of...
Main Authors: | Miroslav Průcha, Petr Czinner, Petra Prokopová |
---|---|
Format: | Article |
Language: | English |
Published: |
Karolinum Press
2016-01-01
|
Series: | Prague Medical Report |
Subjects: | |
Online Access: | https://pmr.lf1.cuni.cz/117/2/0124/ |
Similar Items
-
Ormond’s Disease – IgG4-related Disease
by: Miroslav Průcha, et al.
Published: (2015-01-01) -
An atypical presentation of Ormond’s disease
by: João Carvão, et al.
Published: (2021-12-01) -
Combination of Steroids and Azathioprine in the Treatment of Ormond’s Disease – A Single Centre Retrospective Analysis
by: Miroslav Průcha, et al.
Published: (2016-01-01) -
Ormond's disease - the current state of knowledge about diagnosis and treatment
by: Sara Dankiewicz, et al.
Published: (2022-09-01) -
Retroperitoneal fibrosis – a report of five cases
by: Marta Runowska, et al.
Published: (2017-07-01)