Rosai Dorfman disease: Difference between revisions
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{{Infobox disease | {{Infobox disease | ||
| Name = Rosai-Dorfman disease | | Name = Rosai-Dorfman disease | ||
| DiseasesDB = 31419 | | DiseasesDB = 31419 | ||
| ICD10 = D76.3 ([[ILDS]] D76.360) | | ICD10 = D76.3 ([[ILDS]] D76.360) | ||
| Line 18: | Line 16: | ||
{{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== | ==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}} | '''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}} | ||
==Historica Perspective== | |||
This condition has been named after [[Ronald F. Dorfman]] and [[Juan Rosai]]. The alternative [[eponym]] of this condition is known as Destombes-Rosai-Dorfman syndrome, part of which is named after [[Pierre-Paul Louis Lucien Destombes]]. | |||
Revision as of 19:15, 31 July 2012
| Rosai-Dorfman disease | |
| Classification and external resources | |
| 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
Historica Perspective
This condition has been named after Ronald F. Dorfman and Juan Rosai. The alternative eponym of this condition is known as Destombes-Rosai-Dorfman syndrome, part of which is named after Pierre-Paul Louis Lucien Destombes.
- ↑ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.