Skip to Main content Skip to Navigation
Journal articles

Maladie d'Erdheim-Chester : à propos d'un cas et revue de la littérature. [Erdheim-Chester disease: Report of a case and literature review].

Abstract : 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.
Document type :
Journal articles
Complete list of metadatas

https://www.hal.inserm.fr/inserm-00693604
Contributor : Hervé de Villemeur <>
Submitted on : Wednesday, May 2, 2012 - 6:43:33 PM
Last modification on : Wednesday, May 16, 2018 - 11:24:04 AM

Identifiers

Citation

Paul Prunel, Grégory Verhoest, Sophie Besnard, T. Rohou, Nathalie Rioux-Leclercq, et al.. Maladie d'Erdheim-Chester : à propos d'un cas et revue de la littérature. [Erdheim-Chester disease: Report of a case and literature review].. Progrès en Urologie, Elsevier Masson, 2012, 22 (5), pp.310-2. ⟨10.1016/j.purol.2011.11.003⟩. ⟨inserm-00693604⟩

Share

Metrics

Record views

351