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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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Prunel, Paul | Verhoest, Grégory | Besnard, Sophie | Rohou, T. | Rioux-Leclercq, Nathalie | Bensalah, Karim

Edité par CCSD ; Elsevier Masson -

International audience. 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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