Non-Langerhans cell histiocytosis
| Non-Langerhans cell histiocytosis | |
|---|---|
| Classification and external resources | |
| MeSH | D015616 |
Non-Langerhans cell histiocytosis refers to a family of histiocytosis characterized by the absence of Langerhans cells.[1]
Many manifest cutaneously.[2]
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.[3]
References
- ↑ 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. PMID 15679446.
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