Maladie d'Erdheim-Chester : à propos d'un cas et revue de la littérature. [Erdheim-Chester disease: Report of a case and literature review]. - Archive ouverte HAL Access content directly
Journal Articles Progrès en Urologie Year : 2012

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

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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.
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Dates and versions

inserm-00693604 , version 1 (02-05-2012)

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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, 2012, 22 (5), pp.310-2. ⟨10.1016/j.purol.2011.11.003⟩. ⟨inserm-00693604⟩
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