Combined chest wall and liver hydatid cyst

Feridoun Sabzi, Reza Faraji
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Abstract

The most common location of a hydatid cyst (HC) is the liver, followed by the lungs and other organs. Hydatid cysts in the anterior chest wall are an exceedingly rare complication and much rarer if it is associated with liver HC. A 53-year-old man presented to our clinic with a painless anterior chest wall mass (ACWM). Thoraco-abdominal computed tomography revealed simple cystic masses localized in the ACWM in subcutaneous tissue with no invasion of the peripheral soft tissue and no pulmonary or rib involvement. An echinococcal indirect hemagglutination test was negative. Dermoid cyst was considered as a diagnosis and the encapsulated masses were dissected through its plane in peripheral tissue adhesion and removed completely. Macroscopic and microscopic examination of the specimens confirmed hydatid cysts. Further organ evaluation revealed the liver hydatid cyst. The patient was referred for surgery where he underwent laparotomy and drainage of cyst content and capitonaged into peritoneal cavity. This case report demonstrates that hydatid cysts should be considered as a possible cause for palpable lesions in the chest wall, especially in endemic locations.
合并胸壁肝包虫病
包虫病最常见的部位是肝脏,其次是肺和其他器官。前胸壁的包虫囊肿是一种非常罕见的并发症,如果它与肝HC相关联则更为罕见。一名53岁男性以无痛性前胸壁肿块(ACWM)就诊。胸腹计算机断层扫描显示单纯囊性肿块位于ACWM皮下组织,未侵犯周围软组织,未累及肺或肋骨。棘球蚴间接血凝试验呈阴性。诊断为皮样囊肿,经皮样囊肿外周组织粘连平面剥离包被肿块,完全切除。肉眼及显微镜检查证实为包虫囊肿。进一步的脏器检查显示为肝包虫囊肿。患者接受手术,开腹引流囊肿内容物,并将其放入腹腔。本病例报告表明,包虫囊肿应被认为是胸壁可触及病变的可能原因,特别是在流行的地方。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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