Caso Clínico: Mesotelioma primario de pericardio

Juan Sebastián Sánchez León, Irene Lucía Torres Washima, Anabel Stefanía Cobos Gálvez, Gladis Margarita Molina Alvarado
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Abstract

BACKGROUND: Primary pericardial mesothelioma is an extremely rare mesodermal tumor, among oncological diseases, with a very low incidence. About 350 cases have been described around the world, most of them diagnosed post-mortem. The short term prognosis is poor, regardless of the treatment, which is mostly palliative. We present a case report regarding this pathology. CASE REPORT: 69 year old patient hospitalized with dyspnea and severe anemia. Complementary workup showed pleural effusion and pericardial effusion. Histopathology report of the pericardial fluid revealed pericardial mesothelioma. EVOLUTION: Due to recurrence of pericardial effusion, it was decided to perform pericardiectomy and left pleurectomy as palliative treatment, to alleviate the patient’s symptoms. Chemotherapy was planned after the procedure, but the patient’s general condition deteriorated severely leading to his death. CONCLUSION: Primary pericardial mesothelioma is a rare tumor, whose symptoms are characterized by the associated pericardial effusion, making the diagnosis difficult due to it low incidence. The prognosis is poor in short- term, and there isn’t an established protocol for the treatment with results that showed improve in mortality. KEYWORDS: MESOTHELIOMA, PERICARDIAL EFFUSION, PERICARDIECTOMY, PLEUROTOMY.
临床病例:原发性心包间皮瘤
背景:原发性心包间皮瘤是一种在肿瘤疾病中极为罕见的中胚层肿瘤,发病率极低。全世界约有350例确诊病例,其中大多数是死后确诊的。无论采用何种治疗方法,短期预后都很差,主要是姑息治疗。我们提出一个关于这种病理的病例报告。病例报告:69岁患者因呼吸困难和严重贫血住院。补充检查显示胸腔积液和心包积液。心包液的组织病理学报告显示心包间皮瘤。演变:由于心包积液复发,决定行心包切除术和左胸膜切除术作为姑息治疗,以缓解患者的症状。手术后计划进行化疗,但病人的一般情况严重恶化,导致他死亡。结论:原发性心包间皮瘤是一种罕见的肿瘤,其症状以伴发心包积液为特征,发病率低,诊断困难。短期预后很差,并且没有一个既定的治疗方案,结果显示死亡率有所提高。关键词:间皮瘤,心包积液,心包切除术,胸膜切开术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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