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A Metal-Associated Epithelioid Angiosarcoma: A Case Report and Literature Review
Sean Chan1, Jonathan Horng1, Morgan E Hasegawa1
1Department of Surgery, Division of Orthopaedics University of Hawai'i John A Burns School of Medicine.
Hawai'I Journal of Health & Social Welfare
|June 5, 2026
Summary
Epithelioid angiosarcoma, a rare bone cancer, can develop near orthopedic implants. This case highlights a misdiagnosis of chronic osteomyelitis in a patient with a history of ballistic injury.
Area of Science:
- Orthopedic oncology
- Vascular tumors
- Skeletal malignancies
Background:
- Angiosarcoma is a rare, aggressive bone malignancy (<1% of bone sarcomas).
- Epithelioid angiosarcoma, a subtype, presents with pleomorphic cells and vascular differentiation, often in deep soft tissues.
- Association with orthopedic implants or foreign bodies is exceptionally rare.
Purpose of the Study:
- To report a rare case of epithelioid angiosarcoma.
- To discuss the diagnostic challenges in cases with orthopedic implants and prior trauma.
- To highlight the importance of considering rare malignancies in complex orthopedic cases.
Main Methods:
- Case report presentation.
- Review of patient history including ballistic injury and intramedullary nail fixation.
- Histopathological analysis of the tumor.
Main Results:
- A 54-year-old male presented with epithelioid angiosarcoma.
- The patient had a history of proximal femur ballistic injury and intramedullary nail fixation.
- Initial diagnosis was misconstrued as chronic osteomyelitis.
Conclusions:
- Epithelioid angiosarcoma can arise in the context of orthopedic implants and prior ballistic trauma.
- Misdiagnosis as chronic osteomyelitis can occur, underscoring the need for vigilance.
- This case emphasizes the importance of thorough evaluation for rare bone tumors in patients with complex orthopedic histories.