Congenital Angiosarcoma, a Case Report and Review of Literature

Angiosarcoma, originating from vessels, constitutes about 0.2% to 0.3% of all pediatric soft tissue sarcomas. Prognosis of angiosarcoma is poor and depends on patient’s age, tumor location, size, histological grade and extent of tumor progression.

We report a rare case of a congenital angiosarcoma of scalp with dural and skull bone invasion in a one-month-old boy. His mother noticed the mass 2 days after birth as a very small insignificant nodule, but it grew rapidly afterward.

The treatment consisted of only a wide surgical resection. After 15 months there was no sign of local recurrence or metastasis was noticeable and the tumor showed favorable outcome. This case indicates the possibility of a better clinical behavior in congenital angiosarcoma.