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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.
https://www.hal.inserm.fr/inserm-00693604
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Submitted on : Wednesday, May 2, 2012 - 6:43:33 PM
Last modification on : Tuesday, November 23, 2021 - 2:24:03 PM
Contributor : Hervé de Villemeur Connect in order to contact the contributor
Submitted on : Wednesday, May 2, 2012 - 6:43:33 PM
Last modification on : Tuesday, November 23, 2021 - 2:24:03 PM