Bacha S, Chaouch N, Mlika M, Racil H, Cheikhrouhou S, Chabbou A
Service de pneumologie, pavillon 2, hôpital de pneumo-phtisiologie Abderrahmane Mami, 2080 Ariana, Tunisie.
Service de pneumologie, pavillon 2, hôpital de pneumo-phtisiologie Abderrahmane Mami, 2080 Ariana, Tunisie.
Rev Mal Respir. 2016 Sep;33(7):626-9. doi: 10.1016/j.rmr.2015.10.740. Epub 2015 Nov 17.
Intrathoracic mesothelial cysts are congenital lesions due to an abnormal development of the pericardial coelom. They are usually asymptomatic and found incidentally on chest radiography or computed tomography. As their classic anatomical location is in the cardiophrenic angle, they are also referred to pleuropericardial cysts.
A 50-year-old male presented with a history of chest pain. Physical examination and chest X-ray were normal. Computed tomography (CT) scan revealed a cystic lesion in the posterior and upper mediastinum. The cyst was surgically removed through a posterolateral thoracotomy. Histopathological examination confirmed that it was a mesothelial cyst. The surgical resection of the cyst lead to relief of the thoracic pain over a three-year follow-up period. CT-scan showed an aberrant right subclavian artery or arteria lusoria, which is an anomaly of the aortic arch secondary to abnormal embryogenesis. We know no other report of concurrent ectopic coelomic cyst and aberrant right subclavian artery.
Although the majority of coelomic cysts needs only radiological and clinical follow-up, surgical resection should be performed when the patient is symptomatic or when the diagnosis is uncertain.
胸内间皮囊肿是由于心包体腔发育异常导致的先天性病变。它们通常无症状,在胸部X线或计算机断层扫描时偶然发现。由于其典型的解剖位置在心膈角,它们也被称为胸膜心包囊肿。
一名50岁男性,有胸痛病史。体格检查和胸部X线检查正常。计算机断层扫描(CT)显示后上纵隔有一个囊性病变。通过后外侧开胸手术切除囊肿。组织病理学检查证实为间皮囊肿。在三年的随访期内,囊肿的手术切除使胸痛得到缓解。CT扫描显示有一支迷走右锁骨下动脉,即继发于异常胚胎发育的主动脉弓异常。我们未发现其他关于并发异位体腔囊肿和迷走右锁骨下动脉的报告。
虽然大多数体腔囊肿仅需进行影像学和临床随访,但当患者出现症状或诊断不确定时,应进行手术切除。