Non-Langerhans cell histiocytosis
Non-Langerhans cell histiocytosis refers to a family of histiocytosis characterized by the absence of Langerhans cells.[2]
| Non-Langerhans cell histiocytosis | |
|---|---|
| Other names | Histiocytosis, Non-Langerhans-Cell [1] |
| Specialty | Hematology |
Many manifest cutaneously.[3]
the spectrum of non-langerhans cell histiocytoses include:
- Benign cephalic histiocytosis
- Generalized eruptive histiocytoma
- Indeterminate cell histiocytosis
- Juvenile xanthogranuloma
- Progressive nodular histiocytoma
- Necrobiotic xanthogranuloma
- (Giant Cell) Reticulohistiocytoma
- Multicentric reticulohistiocytosis
- Rosai–Dorfman disease
- Xanthoma disseminatum
- Kikuchi disease
- Erdheim–Chester disease.[4]
References
- "Non-Langerhans-Cell Histiocytosis". NIH. The Genetic and Rare Diseases Information Center (GARD). Retrieved 19 March 2019.
- Weitzman S, Jaffe R (September 2005). "Uncommon histiocytic disorders: the non-Langerhans cell histiocytoses". Pediatr Blood Cancer. 45 (3): 256–64. doi:10.1002/pbc.20246. PMID 15547923.
- Philip T. Cagle; Timothy C. Allen; Roberto Barrios (1 December 2007). Color atlas and text of pulmonary pathology. Lippincott Williams & Wilkins. pp. 210–. ISBN 978-0-7817-8208-1. Retrieved 14 November 2010.
- Rao RN, Chang CC, Uysal N, Presberg K, Shidham VB, Tomashefski JF (February 2005). "Fulminant multisystem non-langerhans cell histiocytic proliferation with hemophagocytosis: a variant form of Erdheim-Chester disease". Arch. Pathol. Lab. Med. 129 (2): e39–43. doi:10.1043/1543-2165(2005)129<e39:FMNCHP>2.0.CO;2 (inactive 2019-10-22). PMID 15679446.
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