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
收藏
页码:310 / 312
页数:3
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