Reticulohistiocytosis From Wikipedia, the free encyclopedia Medical conditionReticulohistiocytosisSpecialtyDermatology Reticulohistiocytosis is a cutaneous condition of which there are two distinct forms:[1]: 718–9 Reticulohistiocytoma Multicentric reticulohistiocytosis Non-X histiocytosis References ↑ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6. vteHistiocytosisWHO-I/Langerhans cell histiocytosis/X-type histiocytosis Letterer–Siwe disease Hand–Schüller–Christian disease Eosinophilic granuloma Congenital self-healing reticulohistiocytosis WHO-II/non-Langerhans cell histiocytosis/Non-X histiocytosis Juvenile xanthogranuloma Hemophagocytic lymphohistiocytosis Erdheim-Chester disease Niemann–Pick disease Sea-blue histiocytosis Benign cephalic histiocytosis Generalized eruptive histiocytoma Xanthoma disseminatum Progressive nodular histiocytosis Papular xanthoma Hereditary progressive mucinous histiocytosis Reticulohistiocytosis (Multicentric reticulohistiocytosis, Reticulohistiocytoma) Indeterminate cell histiocytosis WHO-III/malignant histiocytosis Histiocytic sarcoma Langerhans cell sarcoma Interdigitating dendritic cell sarcoma Follicular dendritic cell sarcoma Ungrouped Rosai–Dorfman disease This cutaneous condition article is a stub. You can help Wikipedia by expanding it.vte Related Articles
