Metachronous Malignant Fibrous Histiocytoma- A Rare Case Report

Authors

  • Amit Yadav Dept. of Pathology, Vardhman Mahavir Medical College & Safdarjung Hospital, New Delhi, India
  • Gireesha Rawal Dept. of Pathology, Vardhman Mahavir Medical College & Safdarjung Hospital, New Delhi, India
  • Indrani Dhawan Dept. of Pathology, Vardhman Mahavir Medical College & Safdarjung Hospital, New Delhi, India
  • Sufian Zaheer Dept. of Pathology, Vardhman Mahavir Medical College & Safdarjung Hospital, New Delhi, India
Abstract:

Malignant fibrous histiocytoma (MFH) is one of the most common types of soft tissue sarcomas in adults. Distant metastases are developed in 30–40% of patients with MFH, with the most common site being the lung. However, metachronous MFH has not been reported previously in literature. This report describes a case of a 30-year-old man, who had two metachronous thigh tumors, both of which were confirmed to be MFH on histopathology and immunohistochemistry evaluations. A contemporary multidisciplinary approach to therapy including surgery, radiation and chemotherapy was advocated. Two primary sites of MFH raised the possibility of a genetic abnormality that could predispose such a patient to develop multiple primary sites of the same tumor.

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Journal title

volume 13  issue 4

pages  474- 478

publication date 2018-09-01

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