Angiosarcoma in the femoral bone: A case report of a rare bone tumor
Yuni Artha Prabowo Putro, Rahadyan Magetsari, Sharfan Anzhari, Thomas Edison Prasetyo, A. Faiz Huwaidi, Kautsar Akbar

TL;DR
This case report describes a rare angiosarcoma in a man's femur, managed with surgery and radiotherapy, highlighting the importance of early diagnosis and treatment.
Contribution
The paper presents a rare case of angiosarcoma in bone and demonstrates successful management using surgery and radiotherapy.
Findings
Angiosarcoma of the bone is rare and challenging to diagnose due to its similarity to other diseases.
Surgery combined with radiotherapy provided positive clinical outcomes in this patient.
Routine clinicopathological conferences aided in accurate diagnosis and treatment planning.
Abstract
Angiosarcoma is a high-grade endothelial sarcoma rarely found in the bones. Challenges lie in its rareness, high mortality, metastasis, and recurrence. The role of radiotherapy and chemotherapy in managing angiosarcoma remains debatable, while surgery stands out as the optimal treatment for local control. We present a patient with angiosarcoma of the bone, managed through a combination of surgery and radiotherapy. A 66-year-old male presented with pain on the right distal femur and was unable to weight bearing after lifting a box. The X-ray showed a fracture and lytic lesion. The patient has lost 5 kg of body weight in the last 3 months. The Clinicopathological Conference (CPC) suspects a malignancy process, prompting us for wide resection, biopsy, and ORIF with cement augmentation. Histopathology and immunohistochemistry results confirmed the diagnosis of angiosarcoma. We decide to…
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Taxonomy
TopicsVascular Tumors and Angiosarcomas · Cardiac tumors and thrombi · Sarcoma Diagnosis and Treatment
