Indeterminate cell histiocytosis

Classification	D ICD-10: D76.3;
External resources	Orphanet: 158019;

Indeterminate cell histiocytosis
Other names	Indeterminate Dendritic Cell Tumor[1]
Specialty	Dermatology

Indeterminate cell histiocytosis is a cutaneous condition felt to be caused by dermal precursors of Langerhans cells.[2]^:720[3]

References

RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Indeterminate cell histiocytosis". www.orpha.net. Retrieved 20 April 2019.
James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 978-0-7216-2921-6.
Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

Histiocytosis (D76.0, 277.89)
WHO-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 histiocyte 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

Classification	D ICD-10: D76.3
External resources	Orphanet: 158019