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一颗“出血的心”:心包血管肉瘤病例报告及文献复习

A bleeding heart: case report and review of pericardial angiosarcoma.

作者信息

Madan Ujjwal, Mahadevia Himil, Sharma Parth, Gunta Satya Preetham, Tawfik Ossama, Fritchie Karen, Magadan Julian

机构信息

University of Missouri Kansas City, Division of Internal Medicine, Kansas City, MO, USA.

Medical College of Wisconsin, Division of Cardiology, Milwaukee, WI, USA.

出版信息

Autops Case Rep. 2024 May 22;14:e2024488. doi: 10.4322/acr.2024.488. eCollection 2024.

Abstract

Primary cardiac tumors are rare. The cardiac sarcomas are the most common malignant cardiac tumors. These tumors have a dismal prognosis with an overall median survival of 25 months. Clinical features include dyspnea, arrhythmias, pericardial effusions, heart failure, and sudden cardiac death. The diagnosis is often challenging. Therefore, the cardiac imaging workup plays a central role in addition to a high clinical suspicion in the setting of atypical presentations that do not respond to standard therapies. The echocardiography, computed tomography, and cardiac MRI are crucial in clinching the diagnosis. Multimodal treatment with surgery, chemotherapy, and radiotherapy has been shown to improve outcomes, as opposed to using either of these modalities alone. We describe the case of a 30-year-old gentleman with COVID-19 infection who developed recurrent hemorrhagic pericardial effusions refractory to standard treatment and was eventually diagnosed as a case of pericardial angiosarcoma after his biopsy revealed the diagnosis and staging was performed using PET-CT-FDG scan. Our case re-emphasizes the importance of considering a malignant etiology early in the course of the disease presentation, especially in recurrent hemorrhagic effusions despite an inflammatory cytologic diagnosis of fluid. It also highlights the place for cardiac CT and MRI to ascertain the location and spread and to plan the further course of treatment. If diagnosed early, the estimated survival time can be prolonged by instituting a multimodal approach.

摘要

原发性心脏肿瘤较为罕见。心脏肉瘤是最常见的恶性心脏肿瘤。这些肿瘤预后不佳,总体中位生存期为25个月。临床特征包括呼吸困难、心律失常、心包积液、心力衰竭和心源性猝死。诊断往往具有挑战性。因此,除了在对标准治疗无反应的非典型表现情况下高度怀疑外,心脏影像学检查起着核心作用。超声心动图、计算机断层扫描和心脏磁共振成像对于确诊至关重要。与单独使用这些治疗方式之一相比,手术、化疗和放疗的多模式治疗已显示可改善预后。我们描述了一名30岁感染新型冠状病毒肺炎的男性患者,他出现了对标准治疗无效的复发性出血性心包积液,活检确诊后经PET-CT-FDG扫描进行分期,最终被诊断为心包血管肉瘤。我们的病例再次强调了在疾病表现过程早期考虑恶性病因的重要性,尤其是在尽管液体的炎症细胞学诊断存在,但仍有复发性出血性积液的情况下。它还突出了心脏CT和MRI在确定位置和扩散以及规划进一步治疗方案方面的作用。如果早期诊断,通过采用多模式方法可延长估计生存时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06fa/11129860/ecc0f3ef24e1/autopsy-14-e2024488-g01.jpg

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本文引用的文献

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