Messaoudi Houssem, Zayène Bochra, Ben Ismail Imen, Lajmi Mokhles, Lahdhili Hatem, Hachicha Saber, Chenik Slim
Department of Cardiac and Thoracic Surgery, The Military Hospital of Instruction of Tunis, Tunisia.
Department of Cardiac and Thoracic Surgery, The Military Hospital of Instruction of Tunis, Tunisia.
Int J Surg Case Rep. 2020;76:130-133. doi: 10.1016/j.ijscr.2020.09.070. Epub 2020 Sep 16.
The lung is the second most commonly affected organ by hydatidosis, and the bilateral involvement is rare even in endemic regions.
We report the case of a 27-year-old patient who presented with right basithoracic pain and cough evolving for three months. Thoracic CT scan revealed two homogeneous, rounded cystic formations enhancing after injection of the contrast media, located in the lateral basal segments of the lower lobe. An abdominal CT scan was performed to rule out a hepatic localization of the hydatid cyst, revealed a cystic formation of the left psoas muscle. The diagnosis of bilateral hydatid lung cyst associated with hydatid psoas muscle location was then made. The patient underwent a two-stage thoracic surgery. The second step involved partial cystectomy of the psoas muscle hydatid cyst via a left iliac incision and using an extraperitoneal approach. The postoperative course was uneventful.
Management of bilateral pulmonary hydatid cyst is controversial. Some authors recommend operating bilateral cysts in two-stage surgery, with an interval of three to four weeks between procedures. The involvement of the psoas muscle is rare and is generally secondary to the rupture of splenic, hepatic or renal hydatid cysts. Generally, its diagnosis is delayed as the latter is most of the time asymptomatic.
Bilateral pulmonary hydatidosis associated with hydatid cyst of the psoas muscle is a rare entity. Radiological investigations and especially CT scan are the mainstay of diagnosis. Surgery remains to be the treatment modality of choice.
肺是包虫病第二常见受累器官,即使在流行地区双侧受累也很罕见。
我们报告一例27岁患者,其右侧胸廓下部疼痛伴咳嗽3个月。胸部CT扫描显示两个均匀的圆形囊性结构,注射造影剂后强化,位于下叶外侧基底段。行腹部CT扫描以排除肝包虫囊肿定位,结果显示左腰大肌有一个囊性结构。由此诊断为双侧肺包虫囊肿合并腰大肌包虫囊肿。患者接受了两阶段胸外科手术。第二步通过左髂切口经腹膜外途径对腰大肌包虫囊肿进行部分囊肿切除术。术后过程顺利。
双侧肺包虫囊肿的治疗存在争议。一些作者建议采用两阶段手术治疗双侧囊肿,手术间隔3至4周。腰大肌受累罕见,通常继发于脾、肝或肾包虫囊肿破裂。一般来说,其诊断会延迟,因为大多数情况下后者无症状。
双侧肺包虫病合并腰大肌包虫囊肿是一种罕见疾病。影像学检查尤其是CT扫描是诊断的主要手段。手术仍然是首选的治疗方式。