| Literature DB >> 22922948 |
Guangjie Chen1, Minju Li, Dehua Wu, Hongfeng Tang, Daxing Tang.
Abstract
Primary splenic angiosarcoma in children is extremely rare and has a very poor prognosis. We reported a 2.5-year-old boy who had this rare entity and hepatic metastasis. The patient presented with left upper quadrant abdominal mass and anemia. The patient received multidisciplinary treatment and died 32 months after splenectomy.Entities:
Mesh:
Year: 2012 PMID: 22922948 DOI: 10.1007/s00383-012-3164-9
Source DB: PubMed Journal: Pediatr Surg Int ISSN: 0179-0358 Impact factor: 1.827