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British Journal of Radiology (2005) 78, 845-847
© 2005 British Institute of Radiology
doi: 10.1259/bjr/23127241

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Case report

Rosai-Dorfman disease: unusual cause of diffuse and massive retroperitoneal lymphadenopathy

K S Sodhi, MD1, S Suri, MD, FICR, DABR1, R Nijhawan, MD2, M Kang, MD1 and V Gautam, MD1

Department of 1 Radiodiagnosis and 2 Cytology & Gynaecological Pathology, Postgraduate Institute of Medical Education and Research (P.G.I.M.E.R.), Chandigarh, 160012 India

Rosai-Dorfman disease (RDD), originally described as sinus histiocytosis with massive lymphadenopathy, is a rare histiocytic proliferative disorder with a distinctive microscopic appearance. Patients usually present with massive cervical lymphadenopathy. However other nodal sites (mediastinal and inguinal) are also frequently involved. The retro-peritoneum is an infrequent site of involvement. This uncommon entity should also be included in the list of differential diagnoses of diffuse and massive lymphadenopathy, which includes includes infectious/granulomatous conditions, lymphomatous and metastatic disease.







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