Department of Pediatric Surgery, Hokkaido University Graduate School of Medicine, Sapporo 060-8638, Japan.
J Pediatr Surg. 2010 Feb;45(2):e13-6. doi: 10.1016/j.jpedsurg.2009.11.018.
Hepatic alveolar echinococcosis (AE) is an endemic disease in certain parts of the world and relatively rare in children. This report describes a 9-year-old girl with hepatic AE invading the diaphragm and directly spreading to the chest and abdominal wall. She was treated by surgical extirpation and albendazole therapy. In advanced hepatic AE, combined therapy of surgical and medical intervention is thought to improve the prognosis.
肝泡型包虫病(AE)是世界某些地区的地方性疾病,在儿童中相对罕见。本报告描述了一例 9 岁女孩患有肝泡型包虫病,侵犯膈肌并直接蔓延至胸腹壁。她接受了手术切除和阿苯达唑治疗。在肝泡型包虫病晚期,手术和药物联合干预被认为可以改善预后。