Rosai Dorfman disease: appearances can be deceptive
- Chandrasekharan Rajasekharan1,
- Narayanan Santhanavally Ratheesh2,
- Rajan Nandinidevi3,
- Rajasekharan Parvathy4
- 1Department of Internal Medicine, Medical College Hospital, Thiruvananthapuram, Kerala, India
- 2Department of Internal Medicine, Government Medical College Hospital, Thiruvananthapuram, Thiruvananthapuram, Kerala, India
- 3Department of Internal Medicine, Government Medical College Hospital, Thiruvananthapuram, Cochin, Kerala, India
- 4Department of Internal Medicine, M.O.S.C Medical College, Kolenchery, Thiruvananthapuram, Kerala, India
- Correspondence to Professor Chandrasekharan Rajasekharan, drcrajasekharan{at}yahoo.com
Summary
A 14-year-old boy was referred to us with a history of progressive painless massive symmetrical cervical lymphadenopathy, provisionally diagnosed as lymphoma. Multiple biopsies were needed, and confirmed the diagnosis of Rosai Dorfman disease (RDD), which is a very rare benign condition. Sinus histiocytosis with massive lymphadenopathy, also known as RDD, manifests as bulky lymphadenopathy in children and young adults. Extranodal sites such as the skin, upper airways, gastrointestinal tract and central nervous system can be involved. There is a characteristic pattern of lymphoid proliferation with a thick fibrous capsule, distention of lymphoid sinuses, accumulation of plasma cells and proliferation of large, often atypical, histiocytes showing emperipolesis is characteristic. The disease is considered to be benign and usually self-limited. We emphasise the need for doing a repeat lymphnode biopsy even if the prior histopathology is suggestive of reactive lypmhnode hyperplasia in every case of persisting lymphadenopathy.








