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| Year:
2013 |
Month:
September
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Volume:
2 |
Issue:
3 |
Page:
22 - 23 |
Rosai-Dorfman Disease- A Surprise diagnosis in Follow up of SCC Pyriform Sinus -Post Surgery and CTRT
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Correspondence
Nandeesh M., Anitha T.K., Santosh R.,
Dr. Nandeesh M.,
#902, DMWIMS Doctors quaters, Naseera nagar, Meppadi, Wayanad, Kerala-673577, India.
Email: nandums2009@gmail.com
Ph: 9544954402 :
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Rosai-Dorfman disease also known as Sinus Histiocytosis with massive Lymphadenopathy (SHML). SHML was first described by Rosai and Dorfman in 1969 (1) and is now considered a non malignant inflammatory disorder in which the precise origin of pathologic cells is still controversial (2). SHML is a rare self-limited pseudolymphomatous disorder of unknown etiology usually present with cervical lymphadenopathy, fever, elevated ESR and hematological abnormalities (3).There is a higher prevalence in males, and among Afro-Caribbeans as compared to Caucasians and Asians. Also, a familial association has been observed in some cases (4). We present a case of 60-year-old male patient with a case of Rosai-Dorfman Disease in Follow up of SCC Pyriform Sinus-Post Surgery and CTRT
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