Abstract
Primary rhabdomyosarcoma of the bone is an extremely rare condition with few examples reported in the literature. We present the case of a 34-year-old male who presented with a lesion in the distal femur with initial imaging features consistent with Ewing sarcoma. Histologically, the lesion consisted of atypical pleomorphic polygonal rhabdomyoblasts demonstrating focal desmin and myogenin expression. A diagnosis of pleomorphic rhabdomyosarcoma was rendered. Despite systemic treatment and surgery, this patient experienced a rapidly progressive disease course. We believe this is only the second report in the orthopedic literature of a case of primary pleomorphic rhabdomyosarcoma of the bone. The key imaging, pathologic, and clinical findings are discussed.
Original language | English (US) |
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Pages (from-to) | 1391-1395 |
Number of pages | 5 |
Journal | Skeletal Radiology |
Volume | 45 |
Issue number | 10 |
DOIs | |
State | Published - Oct 1 2016 |
Keywords
- Adult rhabdomyosarcoma
- Pleomorphic rhabdomyosarcoma
- Primary rhabdomyosarcoma of bone
ASJC Scopus subject areas
- Radiology Nuclear Medicine and imaging