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Case Report

Farooq Ahmed1 , Mohammed Moinuddin2 and R. G. Devani3

1 Postgraduate, Department of Surgery, KBN Institute of Medical Sciences, Kalaburagi, Karnataka, India; farooqmanur@gmail.com

2 Professor, Department of Surgery, KBN Institute of Medical Sciences, Kalaburagi, Karnataka, India

3 Professor and Head, Department of Surgery, KBN Institute of Medical Sciences, Kalaburagi, Karnataka, India

Author for Correspondence :

Dr. Farooq Ahmed

H no 2-909/43/2/53 Farooq Manzil, Bare Hills, Ring road Kalaburagi 585105. farooqmansur@gmail.com

Received Date: 2017-11-12,
Accepted Date: 2017-12-12,
Published Date: 2018-01-30
Year: 2018, Volume: 8, Issue: 1, Page no. 37-39, DOI: 10.26463/rjms.8_1_1
Views: 824, Downloads: 7
Licensing Information:
CC BY NC 4.0 ICON
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0.
Abstract

Sinus Histiocytosis with Massive Lymphadenopathy, also known as Rosai-Dorfman Disease is a rare histiocytic proliferative disorder of unknown etiology. It presents as massive, bilateral, painless cervical lymphadenopathy. We report a case of RosaiDorfman disease in a 11 year old boy who presented with bilateral painless cervical lymohadenopathy. Only a few such cases have been reported in the literature hence this case is being reported for its rarity.

<p>Sinus Histiocytosis with Massive Lymphadenopathy, also known as Rosai-Dorfman Disease is a rare histiocytic proliferative disorder of unknown etiology. It presents as massive, bilateral, painless cervical lymphadenopathy. We report a case of RosaiDorfman disease in a 11 year old boy who presented with bilateral painless cervical lymohadenopathy. Only a few such cases have been reported in the literature hence this case is being reported for its rarity.</p>
Keywords
Cervical Lymphadenopathy, Histiocytosis, Rosai-Dorfman Disease.
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