高级别左房多形性肉瘤：病例报告与文献复习
High-Grade Left Atrial Pleomorphic Sarcoma: Case Report and Review.
作者信息
Zapata Laguado Martin Ignacio, Palacios Rojas Jonathan Orlando, Gómez Lopez Efraín Alonso, Velasco Morales Martha Lucía, Orozco de la Hoz Carlos Eduardo
机构信息
Department of Internal Medicine, Universidad El Bosque, Bogotá, Colombia.
Department of Critical Care, Universidad la Sabana, Bogotá, Colombia.
出版信息
Case Rep Oncol. 2017 Dec 20;10(3):1138-1143. doi: 10.1159/000485561. eCollection 2017 Sep-Dec.
Primary pleomorphic sarcoma of the left atrium is a rare tumor. There is no actual evidence of the management of this pathological entity, so the main treatment is individualized, surgical management being the cornerstone of the treatment. We present a 78-year-old female who had a clinical picture of heart failure, documenting an atrial mass of the left atrium, with high-grade pleomorphic sarcoma revealed in histopathology. The tumor was surgical removed, with no clinical evidence of residual mass. The tumor recurred again within 3 years, to which the patient succumbed.
左心房原发性多形性肉瘤是一种罕见的肿瘤。目前尚无针对这种病理实体的实际治疗证据，因此主要治疗方法是个体化的，手术治疗是治疗的基石。我们报告一名78岁女性，她有心力衰竭的临床表现，经检查发现左心房有肿块，组织病理学显示为高级别多形性肉瘤。肿瘤通过手术切除，术后无残留肿块的临床证据。但肿瘤在3年内再次复发，患者最终因肿瘤去世。
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