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原发性心包横纹肌肉瘤的多模态影像学评估:一例报告

Multimodality imaging assessment of primary pericardial rhabdomyosarcoma: a case report.

作者信息

Li Xingxuan, Cao Yukun, Shao Guozhu, Cui Yue, Li Yumin, Zhang Kailu, Liu Xiaoqing, Shi Heshui

机构信息

Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Department of Radiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Front Cardiovasc Med. 2023 Aug 14;10:1237951. doi: 10.3389/fcvm.2023.1237951. eCollection 2023.

Abstract

Primary pericardial sarcomas are rare and lethal diseases. To date, only a few cases of primary pericardial sarcomas, such as rhabdomyosarcoma (RMS), have been reported. Since the unusual location of RMS in the pericardium makes it challenging to diagnose, precise diagnostic procedures are required. In this study, we present the case of a 23-year-old man who experienced postprandial obstruction and atypical precordial pain that lasted for a week. Echocardiography revealed a heterogeneous isoechoic pericardial mass with a significant pericardial effusion. Contrast-enhanced CT revealed a massive pericardial effusion along with an irregular, defined, heterogeneously enhancing mass that was located between the pericardium and diaphragm. PET-CT imaging showed an intense FDG uptake in the pericardial mass. Furthermore, cardiac MRI demonstrated malignant characteristics of the pericardial mass and provided a detailed visualization of its exact anatomical connection with both cardiac and extracardiac structures. Finally, a pathologic examination of a puncture biopsy specimen confirmed the diagnosis of primary pericardial RMS. Our case emphasizes the importance of multimodal imaging for the differential diagnosis and evaluation of cardiac involvement, while providing clinicians with crucial information for clinical treatment and decision-making.

摘要

原发性心包肉瘤是罕见的致命疾病。迄今为止,仅报道了少数几例原发性心包肉瘤,如横纹肌肉瘤(RMS)。由于RMS在心包中的异常位置使其诊断具有挑战性,因此需要精确的诊断程序。在本研究中,我们报告了一例23岁男性患者,他经历了餐后梗阻和非典型心前区疼痛,持续了一周。超声心动图显示心包内有一个不均匀的等回声肿块,并伴有大量心包积液。增强CT显示大量心包积液,以及一个不规则、边界清晰、不均匀强化的肿块,位于心包和膈肌之间。PET-CT成像显示心包肿块有强烈的FDG摄取。此外,心脏MRI显示了心包肿块的恶性特征,并详细显示了其与心脏和心脏外结构的确切解剖联系。最后,穿刺活检标本的病理检查证实了原发性心包RMS的诊断。我们的病例强调了多模态成像在鉴别诊断和评估心脏受累方面的重要性,同时为临床医生提供了临床治疗和决策的关键信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf16/10461312/ff289801bf0a/fcvm-10-1237951-g001.jpg

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