Abstract
Giant cell tumor of soft tissues (GCT-ST) is a rare entity with unpredictable clinical behavior. However, metastasis and tumor-related death are rarities if these are adequately treated. GCT-ST is required to be distinguished from giant cell-rich tumors of the bone and other soft tissue neoplasms. Coexistence of multiple neurofibromas with GCT-ST is cited in very few literature reports, hence this case report.
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Schedule a callMore From: Archives of Clinical and Experimental Surgery (ACES)
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