CASE REPORT |
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Year : 2020 | Volume
: 7
| Issue : 2 | Page : 74-77 |
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Histiocytic sarcoma: An encounter with a rarity
Neeraja S Kartha, K Sobhanakumari, Predesh Jose
Department of Dermatology, Venereology and Leprosy, Government T. D. Medical College, Alappuzha, Kerala, India
Correspondence Address:
Dr. Neeraja S Kartha Department of Dermatology, Venereology and Leprosy, Government T. D. Medical College, Alappuzha, Kerala India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/ijdpdd.ijdpdd_4_20
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Histiocytic sarcoma is a rare hematolymphoid neoplasm originating from histiocytic cell clones. The lesions can occur in nodal or extranodal sites. A minority of cases present as unique cutaneous lesions. The definitive diagnosis is made by immunohistochemistry. The treatment depends on the severity of the disease. Herein, we report a case of histiocytic sarcoma in a 65-year-old female presenting with subcutaneous swellings and ulcerated coalescing nodules on the forearms and thighs with metastasis to the lung and treated with systemic chemotherapy.
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