Article
Combined Erdheim-Chester disease and Langerhans cell histiocytosis of skin are both monoclonal: a rare case with human androgen-receptor gene analysis.
Journal of the American Academy of Dermatology - 1 Aug 2010
Tsai Jen-Wei, Tsou Jen-Hui, Hung Liang-Yi, Wu Hung-Bo, Chang Kung-Chao
Abstract excerpt
BACKGROUND: Erdheim-Chester disease (ECD) is a rare xanthogranulomatous histiocytic disorder. Langerhans cell histiocytosis (LCH) is a proliferative disorder of histiocytes with a phenotype similar to dendritic Langerhans cells. Both are derived from myeloid stem cells in the bone marrow and, thus, can overlap. OBJECTIVE: We report a rare case of hybrid LCH and ECD of the skin with systemic ECD. METHODS:...
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