Rare Spindle Cell Hemangioma of Bone: A Case Report
DOI:
https://doi.org/10.21276/apalm.3247Keywords:
Bone tumours, femur, spindle cell haemangioma, vascular tumoursAbstract
Spindle cell haemangioma (SCH), a rare vascular tumour usually appears as a cutaneous nodule and subcutaneous nodules in the extremities in adults in 4 th and 5 th decades of life. Its occurrence in bone and paediatric age group is extremely rare. We report a case of SCH arising at the lateral condyle of femur in a 16 year old female. It is important to avoid misdiagnosis as these lesions are considered to be benign, non neoplastic reactive vascular proliferations, with moderate incidence of recurrence.
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