Chen Guangjie, Li Minju, Wu Dehua, Tang Hongfeng, Tang Daxing
Children's Hospital, Zhejiang University School of Medicine, 57 Zhugan Lane, Hangzhou, 310003, China.
Pediatr Surg Int. 2012 Nov;28(11):1147-50. doi: 10.1007/s00383-012-3164-9. Epub 2012 Aug 26.
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.
儿童原发性脾血管肉瘤极为罕见,预后极差。我们报告了一名2.5岁患有这种罕见疾病并伴有肝转移的男孩。该患者表现为左上腹肿块和贫血。患者接受了多学科治疗,脾切除术后32个月死亡。