Xu Z J, Liu T, Chen X B, Jiang S Y, Wang X L, Liu G Z, Wang Y F, Ma X M
Graduate School of Qinghai University, Xining, Qinghai 810001, China.
Co-first authors.
Zhongguo Xue Xi Chong Bing Fang Zhi Za Zhi. 2021 Aug 24;34(3):315-317. doi: 10.16250/j.32.1374.2021088.
Cystic echinococcosis of the abdominal wall is relatively rare. Here, a 54-year-old patient with cystic echinococcosis of the abdominal wall was reported, who was admitted to hospital due to presence of abdominal mass for one year complicated by skin ulceration of the mass for 5 days. The case was initially diagnosed as cystic echinococcosis of the abdominal wall and given sub-abdominal echinococcosis cystectomy. Post-surgical pathological examinations revealed cystic echinococcosis (type of a single locule and multiple daughter cysts). This case report aimed to provide insights into the clinical diagnosis and treatment of cystic echinococcosis of the abdominal wall.
腹壁囊型包虫病相对少见。本文报道了一名54岁腹壁囊型包虫病患者,因腹部肿物1年并肿物皮肤溃疡5天入院。该病例最初诊断为腹壁囊型包虫病,并接受了腹下包虫囊肿切除术。术后病理检查显示为囊型包虫病(单房性及多个子囊型)。本病例报告旨在为腹壁囊型包虫病的临床诊断和治疗提供见解。