一例罕见的原发性心脏人工瓣膜相关淋巴瘤

Sagila George, B. Gehrs, S. Srour
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引用次数: 1

摘要

原发性心脏肿瘤是极为罕见的肿瘤,发病率低于0.4%,约占心脏肿瘤的2%,不到结外淋巴瘤的0.5%。1,4-6涉及心脏瓣膜的原发性淋巴瘤由于其罕见性,在少数病例报告和小病例系列中有描述。7-10大多数PCL病例表现为充血性心力衰竭或心律失常,11,而原发性瓣膜相关淋巴瘤(PV-AL)通常是在瓣膜修复或置换过程中偶然诊断出来的。病理生理学尚不清楚,但少数病例与EB病毒(EBV)有关。7文献中先前描述的病例总体预后较差,迄今为止没有标准化的治疗方法。我们在这里提供了一个罕见的原发性人工瓣膜相关心脏大B细胞淋巴瘤病例,该病例在瓣膜修复后通过辅助化疗成功治疗,并取得了良好的长期疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An unusual case of primary cardiac prosthetic valve-Associated lymphoma
Primary cardiac tumors are extremely rare neoplasms with an incidence of less than 0.4%.1-3 Primary cardiac lymphoma (PCL), the majority of which is non-Hodgkin lymphoma, accounts for around 2% of cardiac tumors and less than 0.5% of extranodal lymphomas.1,4-6 Primary lymphoma involving cardiac valves has been described in few case reports and small case series owing to its rarity.7-10 Most cases of PCL present with manifestations of congestive heart failure or cardiac arrhythmias,11 whereas primary valve-associated lymphoma (PV-AL) is usually diagnosed incidentally during valve repair or replacement. The pathophysiology remains unclear, but a few cases have been associated with Epstein Barr virus (EBV).7 Cases previously described in the literature carried an overall poor prognosis and to date there is no standardized treatment approach. We provide here an unusual case of primary prosthetic valve-associated cardiac large B-cell lymphoma, which was successfully treated with adjuvant chemotherapy after valve repair and which resulted in an excellent long-term outcome.
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