| Literature DB >> 11509804 |
M André1, I Delèvaux, B de Fraissinette, J Ponsonnaille, N Costes Chalret, B Wechsler, J C Piette, O Aumaître.
Abstract
Erdheim-Chester disease is a rare form of non-Langerhans' cell histiocytosis. This disorder is characterized by a bone involvement and several extraskeletal manifestations. We describe the case of a patient with a pleural and pericardial effusion leading to tamponade. Pathological examination of pericardium and mediastinal adenopathy was normal. The abdominal computed tomography scan showed two enlarged kidneys suggestive of Erdheim-Chester disease. Bone scan scintigraphy demonstrated symmetrical increased labeling of the long bones. The biopsy of perirenal soft tissue confirmed the diagnosis of Erdheim-Chester disease. Copyright 2001 S. Karger AG, BaselEntities:
Mesh:
Year: 2001 PMID: 11509804 DOI: 10.1159/000046267
Source DB: PubMed Journal: Am J Nephrol ISSN: 0250-8095 Impact factor: 3.754