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Primary Cardiac Epithelioid Angiosarcoma in a Latin American Patient: Case Report and Literature Review

机译:拉丁美洲患者的原发性心脏上皮样血管肉瘤:病例报告和文献复习

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摘要

Cardiac angiosarcoma is a rare and clinically challenging pathology. It is a high-grade primary malignant tumor of the heart tissue that has many variants, of which the epithelioid variant is rarely present in the heart or the great vessels. As with many other cardiac tumors, it is mainly a diagnosis of exclusion and the initial diagnostic test is an echocardiogram followed by a biopsy with immunohistochemistry analysis to ascertain the type of tumor. The differential diagnosis of cardiac tumors is challenging due to the overlapping clinical manifestations with different cardiac tumors and systemic diseases. Cardiac angiosarcomas are often aggressive with a poor prognosis even with treatment. Herein, we present a case of the epithelioid variant of a cardiac angiosarcoma in addition to a thorough review of the recent literature on the clinical manifestation, diagnosis, and treatment of this type of tumors.
机译:心脏血管肉瘤是一种罕见的临床挑战性病理。它是心脏组织的高级原发性恶性肿瘤,具有许多变体,其中上皮样变体很少出现在心脏或大血管中。与其他许多心脏肿瘤一样,它主要是排除诊断,最初的诊断检查是超声心动图,然后进行活检并进行免疫组织化学分析以确定肿瘤的类型。由于不同的心脏肿瘤和全身性疾病的临床表现重叠,对心脏肿瘤的鉴别诊断具有挑战性。即使进行治疗,心脏血管肉瘤通常也具有侵袭性,预后差。在此,除了对这类肿瘤的临床表现,诊断和治疗的最新文献进行全面回顾之外,我们还介绍了心脏血管肉瘤上皮样变体的病例。

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