Rosai-Dorfman Disease.

dc.contributor.authorSharma, Sindhu
dc.contributor.authorBhardwaj, Subhash
dc.contributor.authorHans, Deepa
dc.date.accessioned2016-02-05T06:40:57Z
dc.date.available2016-02-05T06:40:57Z
dc.date.issued2010-10
dc.description.abstractRosai-Dorfman Disease (RDD) or Sinus Histiocytosis with massive lymhadenopathy (SHML) is a rare, benign proliferative disorder of histiocytes, sometimes showing familial incidence. It is mainly characterized by painless bilateral cervical lymph node enlargement and is often associated with fever and leucocytosis. It presents in the first or second decades of life, though any age group can be affected. Without the awareness about RDD, the diagnosis of RDD is unexpected especially in South East Asian Countries where certain lymphadenopathies such as tuberculosis, metastatic nasopharayngeal carcinoma and lymphomas are common. RDD is commonly missed and so its revision would seem worthwhile, this case illustrating the disappearance of the lymphadenopathy without treatment.en_US
dc.identifier.citationSharma Sindhu, Bhardwaj Subhash, Hans Deepa. Rosai-Dorfman Disease. JK Science Journal of Medical Education and Research. 2010 Oct-Dec; 12(4): 194-196en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/171943
dc.language.isoenen_US
dc.source.urihttps://www.jkscience.org/archive/volume124/Rosai-Dorfman%20Disease.pdfen_US
dc.subjectSinus histiocytosis with massive lymphadenopathy (SHML)en_US
dc.subjectLymphophagocytosis. Emperipolesisen_US
dc.subjectRosai- Dorfman disease (RDD)en_US
dc.titleRosai-Dorfman Disease.en_US
dc.typeArticleen_US
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