Erdheim-Chester disease: Report of a case and literature review

被引：1

作者：

Prunel, P. ^{[1
]}

Verhoest, G. ^{[1
]}

Besnard, S. ^{[2
]}

Rohou, T. ^{[3
]}

Rioux-Leclercq, N. ^{[4
]}

Bensalah, K. ^{[1
]}

机构：

[1] CHU Rennes, Hop Pontchaillou, Serv Urol, F-35033 Rennes, France

[2] CHU Rennes, Hop Pontchaillou, Serv Med Interne, F-35033 Rennes, France

[3] CHU Rennes, Hop Pontchaillou, Serv Radiol, F-35033 Rennes, France

[4] CHU Rennes, Hop Pontchaillou, Serv Anat & Cytol Pathol, F-35033 Rennes, France

来源：

PROGRES EN UROLOGIE | 2012年 / 22卷 / 05期

关键词：

Erdheim-Chester disease; Hystiocytose; Retroperitonale fibrosis;

D O I：

10.1016/j.purol.2011.11.003

中图分类号：

R5 [内科学]; R69 [泌尿科学（泌尿生殖系疾病）];

学科分类号：

1002 ; 100201 ;

摘要：

The Erdheim-Chester disease is a rare non-Langerhans hystiocytose acquired in adults. It results from a xanthogranulomatous infiltration, consists of histioccytes foamy and is characterized by heterogeneous systemic manifestations. The most frequent clinical manifestations of the disease are the bone with a long bone uptake on bone scintigraphy99Tc (Dion et al., 2006 [1]) and urological damage with an array of pseudo retroperitoneal fibrosis. We report the case of a 64-year-old man in whom was founded in the course of acute obstructive renal disease with Erdheim-Chester pseudofibrose retroperitoneal. (C) 2011 Elsevier Masson SAS. All rights reserved.

引用

页码：310 / 312

页数：3

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