Department of General Surgery, Harran University Faculty of Medicine, Sanliurfa, Turkey.
J Cardiothorac Surg. 2024 Oct 7;19(1):596. doi: 10.1186/s13019-024-03066-2.
Hydatid cysts, caused by Echinococcus species, are zoonotic diseases frequently observed in endemic regions worldwide, including Turkey. It is most commonly localized in the liver, followed by the lungs. Anaphylaxis and peritonitis, which develop after cyst rupture, are the most significant complications observed in these patients. Early diagnosis and prompt surgical intervention are extremely important. This study presented an extremely rare case of a hepatic hydatid cyst ruptured into the thorax, which may have high morbidity and mortality. A 24-year-old male patient presented to our emergency department with cough, dyspnea, fever, and allergy symptoms. He had a history of hepatic hydatid cyst surgery 5 years ago. Physical examination revealed urticarial lesions on the skin. The body temperature was 39 °C, and the pulse rate was 120 beats/min. Laboratory tests revealed leukocytosis and elevated C-reactive protein. Contrast-enhanced thoracic and abdominal computed tomography was performed. Diagnostic tests revealed that the patient had a ruptured hepatic hydatid cyst in the right thoracic cavity; hence, he was scheduled for emergency surgery. Laparotomy was performed via a right subcostal incision, and the ruptured cyst was located. It was understood that this cyst had fistulized into the diaphragm during a chronic process and subsequently ruptured acutely into the thorax. Partial cystectomy was performed for a ruptured liver cyst. The diaphragm was repaired, and catheters were placed in the thorax and abdomen for drainage. There were no other postoperative complications. Rupture of hydatid cyst disease is frequently observed in endemic regions. The rupture of a hepatic hydatid cyst into the thorax is an extremely rare event. In patients presenting with pulmonary symptoms who have a history of hepatic hydatid cyst surgery, the abdomen should always be thoroughly evaluated, and emergency surgery should be performed if required.
包虫囊肿由细粒棘球绦虫引起,是一种在包括土耳其在内的世界范围内流行的人畜共患疾病。它最常发生在肝脏,其次是肺部。过敏反应和腹膜炎是这些患者最常见的并发症,这些并发症发生在囊肿破裂后。早期诊断和及时手术干预非常重要。本研究报告了一例极其罕见的肝包虫囊肿破裂入胸腔的病例,这种情况可能具有较高的发病率和死亡率。一名 24 岁男性因咳嗽、呼吸困难、发热和过敏症状到急诊就诊。他 5 年前曾因肝包虫囊肿接受过手术。体格检查显示皮肤有荨麻疹样病变。体温为 39°C,脉搏率为 120 次/分。实验室检查显示白细胞增多和 C 反应蛋白升高。进行了增强型胸部和腹部计算机断层扫描。诊断检查显示患者右侧胸腔有破裂的肝包虫囊肿,因此安排了紧急手术。通过右肋下切口进行剖腹手术,并找到了破裂的囊肿。据了解,该囊肿在慢性过程中已与膈肌相通,并随后急性破裂入胸腔。对破裂的肝囊肿进行部分囊肿切除术。修复了膈肌,并在胸部和腹部放置了引流管。术后无其他并发症。包虫囊肿病在流行地区经常破裂。肝包虫囊肿破裂入胸腔是一种极其罕见的事件。对于有肝包虫囊肿手术史且出现肺部症状的患者,应始终彻底评估腹部,并在需要时进行急诊手术。