Yamamoto Yoichi, Sakamoto Yuzuru, Kamiyama Toshiya, Nagatsu Akihisa, Asahi Yoh, Orimo Tatsuya, Kakisaka Tatsuhiko, Kamachi Hirofumi, Otsuka Takuya, Mitsuhashi Tomoko, Taketomi Akinobu
Department of Gastroenterological Surgery I, Hokkaido University Hospital, North 14, West 5, Kita-ku, Sapporo, 060-8648, Japan.
Department of Surgical Pathology, Hokkaido University Hospital, North 14, West 5, Kita-ku, Sapporo, 060-8648, Japan.
Surg Case Rep. 2022 Apr 8;8(1):63. doi: 10.1186/s40792-022-01417-6.
Alveolar echinococcosis (AE) is a rare parasitic disease caused by the larva of Echinococcus multilocularis. It nearly always occurs in the liver, and cardiac involvement is extremely rare. Liver resection is the most effective intervention for AE because the only potentially curative treatment is removal of the lesion. Even when complete resection is not performed, long-term survival can be expected after surgical removal of most of the lesion with lifelong administration of albendazole (ABZ).
A 64-year-old man who lived in Hokkaido was referred to our hospital due to abnormalities in biliary enzymes. According to the findings from enhanced computed tomography and magnetic resource imaging of the abdomen, transthoracic echocardiography and serologic tests, he was diagnosed with hepatic AE with rupture into the pericardium. He underwent extended left hemi-hepatectomy with reconstruction of the inferior vena cava and opening of the pericardium with drainage as reduction surgery. Pathological examination revealed echinococcal infection in the pericardium as well as the liver. He started chemotherapy with 400 mg ABZ per Day 67 days after surgery. Although the surgical margin was positive in the pathological findings, he was alive 19 months later with no regrowth of the echinococcal lesion.
AE with cardiac involvement is extremely rare. Even if the complete removal of cardiac-involved AE is not possible, surgical debulking with lifelong ABZ treatment can successfully manage the disease.
肺泡型棘球蚴病(AE)是一种由多房棘球绦虫幼虫引起的罕见寄生虫病。几乎总是发生在肝脏,累及心脏极为罕见。肝切除术是治疗AE最有效的干预措施,因为唯一可能治愈的方法是切除病灶。即使未进行完整切除,在手术切除大部分病灶并终身服用阿苯达唑(ABZ)后,也有望实现长期生存。
一名居住在北海道的64岁男性因胆汁酶异常转诊至我院。根据腹部增强计算机断层扫描和磁共振成像、经胸超声心动图及血清学检查结果,他被诊断为肝AE并破入心包。他接受了扩大左半肝切除术,同时重建下腔静脉并打开心包引流作为减瘤手术。病理检查显示心包和肝脏均有棘球蚴感染。术后67天,他开始每天服用400mg ABZ进行化疗。尽管病理检查显示手术切缘阳性,但19个月后他仍存活,棘球蚴病灶无复发。
累及心脏的AE极为罕见。即使无法完全切除累及心脏的AE,手术减瘤并终身接受ABZ治疗也可成功控制该病。