Gonjilashvili Nana, Gagnidze Ekaterine, Ansar Arwa Fareah, Gonjilashvili Ana
Tbilisi State Medical University, Faculty of Medicine, Tbilisi, Georgia.
Jo Ann University Hospital, Department of Cardiology, Tbilisi, Georgia.
Eur J Case Rep Intern Med. 2025 Jul 16;12(8):005667. doi: 10.12890/2025_005667. eCollection 2025.
Cardiac involvement by is extremely rare, accounting for less than 2% of all hydatid disease cases. When it occurs, it commonly affects the left ventricle, while valvular involvement is exceedingly unusual.
We present the case of a 74-year-old woman from rural Georgia who developed progressive exertional dyspnoea and fatigue. Physical examination revealed multiple murmurs, and transthoracic echocardiography identified a mobile, hyperechoic mass attached to the posterior mitral valve leaflet. Transoesophageal echocardiography raised suspicion for a myxoma or vegetation, and surgical excision was pursued due to embolic risk. Intraoperatively, a teardrop-shaped cystic mass containing multiple daughter cysts was found on the P2 segment of the mitral valve. Histopathology confirmed a hydatid cyst, consistent with cardiac echinococcosis. The patient underwent successful segmental excision of the cyst with mitral valve repair and tricuspid annuloplasty. Her postoperative course was complicated by atrial fibrillation and new-onset type 2 diabetes mellitus. She was treated with albendazole and discharged in stable condition.
This report highlights a rare instance of isolated mitral valve echinococcosis, initially misdiagnosed as a myxoma. It underscores the importance of considering parasitic aetiologies in the differential diagnosis of intracardiac masses, particularly in patients with rural backgrounds.
Mitral valve involvement in cardiac echinococcosis is exceedingly rare and may clinically and radiographically mimic myxomas or vegetations.Hydatid disease should be considered in the differential diagnosis of intracardiac masses, especially in patients with epidemiologic exposure to livestock or dogs.Early recognition and surgical intervention, coupled with antiparasitic therapy, are essential for optimal outcomes in rare valvular hydatid disease.
心脏包虫病极为罕见,占所有包虫病病例的比例不到2%。发病时,通常累及左心室,而累及瓣膜的情况极为罕见。
我们报告了一名来自佐治亚州农村的74岁女性病例,她出现了进行性劳力性呼吸困难和疲劳。体格检查发现多处杂音,经胸超声心动图检查发现一个活动的、高回声团块附着于二尖瓣后叶。经食管超声心动图检查怀疑是黏液瘤或赘生物,由于存在栓塞风险,遂进行手术切除。术中,在二尖瓣P2段发现一个泪滴形囊性肿物,内有多个子囊。组织病理学证实为包虫囊肿,符合心脏棘球蚴病。患者成功接受了囊肿节段性切除,并进行了二尖瓣修复和三尖瓣环成形术。术后出现房颤和新发2型糖尿病等并发症。给予阿苯达唑治疗后,患者病情稳定出院。
本报告强调了孤立性二尖瓣棘球蚴病这一罕见病例,最初被误诊为黏液瘤。它强调了在心脏内肿物的鉴别诊断中考虑寄生虫病因的重要性,特别是对于有农村背景的患者。
二尖瓣受累的心脏棘球蚴病极为罕见,在临床和影像学上可能类似于黏液瘤或赘生物。在心脏内肿物的鉴别诊断中应考虑包虫病,尤其是在有接触家畜或狗的流行病学史的患者中。早期识别和手术干预,结合抗寄生虫治疗,对于罕见的瓣膜性包虫病取得最佳治疗效果至关重要。