Rosai Dorfman Disease with malignant transformation to Histiocytic Sarcoma: A diagnostic conundrum

Author:

Thakur Shilpi1,Abraham Reema M.2,Pushpam Deepam3,Ahmed Shamim4,Mallick Saumyaranjan1

Affiliation:

1. Department of Pathology, All India Institute of Medical Sciences, New Delhi, India

2. Department of Hematology, All India Institute of Medical Sciences, New Delhi, India

3. Department of Medical Oncology, All India Institute of Medical Sciences, New Delhi, India

4. Department of Nuclear Medicine, All India Institute of Medical Sciences, New Delhi, India

Abstract

ABSTRACT Histiocytic disorders mostly occur as de-novo nodal or extranodal benign masses with rare secondary malignant transformation. A 10-year-old female presented with 10-cm cervical swelling since 9 months associated with fever. Computed tomography revealed left cervical lymphadenopathy and bilateral lung nodules. Lymph node excision biopsy showed effacement of architecture by atypical histiocytes with marked nuclear pleomorphism and frequent mitosis. Focal areas showed mature histiocytes with emperipolesis. The cells were immunopositive for CD68, CD163, and S100 (focal), whereas they were negative for Langerin and CD1a. The Ki67 proliferative index was 30%. A diagnosis of histiocytic sarcoma in a background of Rosai-Dorfman disease was made.

Publisher

Medknow

Reference10 articles.

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5. Sinus histiocytosis with massive lymphadenopathy--a review of seven cases;Agarwal;Indian J Pathol Microbiol,2006

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