先天性动静脉瘘少见。最近我们收治一例,病变累及右臀及右下肢,臀部并发巨大血管瘤,临床罕见,手术治愈出院。随防二年健在。现报告如下:病例简介患者,女,17岁,右臀包块及右下肢增粗9年,门诊诊断“神经纤维瘤”,于1987年10年收住院。患者于1978年始,于右臀、右小腿外侧出现一包块,渐增大,近三年生长更快,患部感酸痛,坠 Congenital arteriovenous fistula is rare. Recently, we treated one patient. The lesions involved the right buttocks and the right lower limbs. The hips were complicated with massive hemangiomas. Clinically rare, the patients were cured and discharged. After two years of prevention. The report is as follows: Case Description Patients, females, 17 years old, with right hip mass and right lower extremity thickened for 9 years, diagnosed with “neural fibroids” in the outpatient department and admitted to hospital in 1987. In 1978, the patient developed a mass on the outside of the right hip and right lower leg, gradually increased, and grew faster in the past three years.