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Epithelioid Angiosarcoma in Femur: A Case Presentation.
Yunus Oc1, Bekir Eray Kilinc2, Rodi Ertugrul1
1Orthopaedics and Traumatology Department, Sisli Hamidiye Etfal Training and Research Hospital, Istanbul, Turkey.
Epithelioid angiosarcoma, a rare bone tumor mimicking carcinoma, was diagnosed in a young male with hip pain. Imaging suggested an aneurysmal bone cyst, highlighting diagnostic challenges.
Area of Science:
- Oncology
- Pathology
- Radiology
Background:
- Primary malignant vascular tumors are rare, comprising <1% of primary bone tumors.
- Epithelioid angiosarcoma is an uncommon subtype with an epithelioid phenotype, often mimicking carcinomas.
- These tumors typically occur in extraskeletal locations, with bone involvement being rare.
Observation:
- A 31-year-old male presented with left hip pain.
- Radiography revealed a cystic, expansile mass in the trochanteric region of the femur.
- CT showed a 7 cm cystic mass with septa; MRI suggested an aneurysmal bone cyst.
Findings:
- Histological examination and biopsy confirmed epithelioid angiosarcoma.
- The excised specimen further verified the preoperative diagnosis.
- This case highlights the rarity of epithelioid angiosarcoma in bone.
Implications:
- Accurate diagnosis of epithelioid angiosarcoma requires careful histological evaluation.
- Radiological features can mimic other bone lesions, necessitating a high index of suspicion.
- Understanding rare bone tumor presentations is crucial for effective patient management.
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