Multimodal imaging for the diagnosis of cardiac alveolar echinococcosis: a case report.

IF 2.3 3区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS BMC Cardiovascular Disorders Pub Date : 2025-02-17 DOI:10.1186/s12872-025-04531-z
Mengdie Zhu, Xukun Gao, Xiaoping Wang, Li Meng
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Abstract

Background: 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.

Conclusion: 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.

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多模态影像诊断心脏肺泡包虫病1例。
背景:原发性心脏棘球蚴病是罕见的,而心脏肺泡棘球蚴病则更为罕见和罕见。报告的病例极为有限,多模态成像为治疗和决策提供了重要指导。我们报告一例心脏肺泡包虫病。31岁男性患者,无明显病史,诊断为纵隔占位性病变。经胸超声心动图显示右心房右侧前方有囊性肿块,增强扫描未见增强。多层螺旋ct及心脏磁共振示右心房右侧一囊性占位性病变,病灶边缘轻度强化,增强扫描可见多发小泡。临床医生对疑似心包虫病的患者进行了手术,并成功切除了病变。最终,术后组织病理学检查显示心脏肺泡包虫病。患者术后定期口服阿苯达唑片并定期随访,恢复良好出院。结论:我们报告一例具有多模态影像特征和治疗策略的心脏肺泡包虫病,这是一种极为罕见的心脏占位性疾病。多模态影像对本病的诊断有很大的帮助,手术切除和组织病理学诊断是必不可少的。术后根据组织学检查结果进行治疗及随访。本罕见病例强调结合临床、多模式影像及病理资料综合诊断心脏肺泡包虫病。
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来源期刊
BMC Cardiovascular Disorders
BMC Cardiovascular Disorders CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
3.50
自引率
0.00%
发文量
480
审稿时长
1 months
期刊介绍: BMC Cardiovascular Disorders is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of disorders of the heart and circulatory system, as well as related molecular and cell biology, genetics, pathophysiology, epidemiology, and controlled trials.
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