Rosai Dorfman disease: Difference between revisions
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{{SK}} Sinus histiocytosis with massive lymphadenopathy, SHML, Destombes-Rosai-Dorfman syndrome, familial Rosai–Dorfman disease, familial SHML | {{SK}} Sinus histiocytosis with massive lymphadenopathy, SHML, Destombes-Rosai-Dorfman syndrome, familial Rosai–Dorfman disease, familial SHML | ||
==Overview== | |||
'''Rosai–Dorfman disease''' is a rare disorder of [[idiopathic|unknown etiology]] that is characterized by abundant [[histiocyte]]s in the [[lymph node]]s throughout the body.<ref name="Andrews">{{cite book |author=James, William D.; Berger, Timothy G.; et al. |title=Andrews' Diseases of the Skin: clinical Dermatology |publisher=Saunders Elsevier |location= |year=2006 |pages= |isbn=0-7216-2921-0 |oclc= |doi= |accessdate=}}</ref>{{rp|747}} | |||
Revision as of 19:13, 31 July 2012
| Rosai-Dorfman disease | |
| Classification and external resources | |
| |
|---|---|
| Micrograph of a lymph node involved by Rosai-Dorfman disease showing emperipolesis. H&E stain. | |
| ICD-10 | D76.3 (ILDS D76.360) |
| DiseasesDB | 31419 |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Raviteja Guddeti, M.B.B.S. [2]
Synonyms and keywords: Sinus histiocytosis with massive lymphadenopathy, SHML, Destombes-Rosai-Dorfman syndrome, familial Rosai–Dorfman disease, familial SHML
Overview
Rosai–Dorfman disease is a rare disorder of unknown etiology that is characterized by abundant histiocytes in the lymph nodes throughout the body.[1]:747
- ↑ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.