Zhu Mengdie, Gao Xukun, Wang Xiaoping, Meng Li
Department of Radiology, Affiliated Hospital of Qinghai University, Tongren Road No.29, Xining, 810001, People's Republic of China.
BMC Cardiovasc Disord. 2025 Feb 17;25(1):107. doi: 10.1186/s12872-025-04531-z.
Primary cardiac echinococcosis is rare, and cardiac alveolar echinococcosis is even rarer and more unusual. Reported cases of this disease are extremely limited, and multimodal imaging provides an important guide to treatment and decision-making. We report a case of cardiac alveolar echinococcosis. A 31-year-old male patient with no significant history was diagnosed to have a space-occupying lesion in the mediastinum. Transthoracic echocardiography showed a cystic mass anterior to the right lateral aspect of the right atrium, which did not show enhancement on the enhanced scan. Multidetector computed tomography (MDCT) and cardiac magnetic resonance showed a cystic space-occupying lesion in the right lateral aspect of the right atrium, with mild enhancement of the edges of the lesion and multiple small vesicles on the enhancement scan. Clinicians operated on the patient under suspicion of cardiac echinococcosis and successfully removed the lesion. Ultimately, postoperative histopathologic examination revealed cardiac alveolar echinococcosis. The patient recovered well and was discharged with regular postoperative oral albendazole tablets and regular follow-up reviews.
We report a case of cardiac alveolar echinococcosis with multimodal imaging features and therapeutic strategies, an extremely rare cardiac occupying disease. Multimodal imaging is of great help in the diagnosis of this disease, and surgical resection and histopathological diagnosis are essential. After surgery, treatment and follow-up will be carried out based on the results of the histological examination. This rare case emphasizes the integrated diagnosis of cardiac alveolar echinococcosis with clinical, multimodal imaging and pathologic data.
原发性心脏包虫病较为罕见,而心脏泡型包虫病更为罕见且不常见。该疾病的报道病例极为有限,多模态成像为治疗和决策提供了重要指导。我们报告一例心脏泡型包虫病病例。一名31岁无显著病史的男性患者被诊断为纵隔占位性病变。经胸超声心动图显示右心房右侧缘前方有一囊性肿块,增强扫描未见强化。多排螺旋计算机断层扫描(MDCT)和心脏磁共振成像显示右心房右侧缘有一囊性占位性病变,病变边缘轻度强化,增强扫描可见多个小囊泡。临床医生在怀疑心脏包虫病的情况下对患者进行了手术,并成功切除了病变。最终,术后组织病理学检查显示为心脏泡型包虫病。患者恢复良好,出院时带常规术后口服阿苯达唑片并定期进行随访复查。
我们报告一例具有多模态成像特征及治疗策略的心脏泡型包虫病病例,这是一种极为罕见的心脏占位性疾病。多模态成像对该疾病的诊断有很大帮助,手术切除及组织病理学诊断至关重要。术后将根据组织学检查结果进行治疗及随访。这一罕见病例强调了心脏泡型包虫病需结合临床、多模态成像及病理数据进行综合诊断。