Rare case of both kidneys spontaneous rupture in
patient with retroperitoneal fibrosis (Ormond’s disease) Article published in Urologia Polska 2008/61/4.
authors
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Radosław Starownik1, Krzysztof Bar1, Anna Bednarek-Skublewska2, Waldemar Białek1, Jacek Ki¶1, Dariusz Borowiec1, Waldemar Lasota1
- 1Katedra i Klinika Urologii i Onkologii Urologicznej Uniwersytetu Medycznego w Lublinie
2Katedra i Klinika Nefrologii Uniwersytetu Medycznego w Lublinie
keywords
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kidney retroperitoneal fibrosis
summary
- Retroperitoneal fibrosis (Ormond’s disease, RPF) is relatively unusual condition characterized by widespread fibrosis, usually occurring
- in the retroperitoneum. RPF is composed of proliferating fibrous tissue dissecting through adipose tissue the abdominal aorta and
- branches of common iliac vessels artery region. This fibrotic tissue usually involves the ureters causing their compression with secondary
- hydronephrosis.
- We introduce case of both kidneys spontaneous rupture in patient with Ormond’s disease.
references
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