Case Report (n=1)
No
Total excision of a rare congenital primary cerebral angiosarcoma in an infant resulted in an uneventful recovery and no recurrence at 11 months.
Answers are grounded in this paper and cite their sources.
May support resectability of neonatal cerebral angiosarcoma; leaves open need for longer follow-up and multicenter series.
Reports of angiosarcoma arising in the central nervous system are rare. The authors present the case of a 30-day-old infant with clinical manifestations of projectile vomiting and tense anterior fontanelle resulting from a left frontotemporal tumor. Total excision of this highly vascular, well-circumscribed tumor was performed without incident, and histopathological examination revealed a malignant angiosarcoma. Immunohistochemical reaction of the neoplastic cells was diffusely positive for endothelium-specific antigens including factor VIII-related antigen, CD31, and CD34. The final diagnosis of congenital primary cerebral angiosarcoma was thus confirmed. The patient's postoperative course was uneventful, and he was discharged 2 weeks after the operation. He was in good condition with no sign of recurrence after 11 months; follow-up computerized tomography, magnetic resonance (MR) imaging, and abdominal ultrasonography studies demonstrated no tumor regrowth. The characteristic findings for this tumor on MR imaging, the immunohistochemical findings, and surgical outcome are discussed.
No takes yet. Share an insight, caveat, or question.
Suzuki et al. (2000) conducted a case report in Congenital primary cerebral angiosarcoma (n=1). Surgical resection was evaluated on Tumor recurrence.
Synapse has enriched 10 related papers. Consider them for comparative context: