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Malignant pleural mesothelioma presenting as spontaneous pneumothorax: a case series and review.

机译:恶性胸膜间皮瘤表现为自发性气胸:病例系列和审查。

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BACKGROUND: Malignant pleural mesothelioma (MPM) is thought to arise from the mesothelial cells that line the pleural cavities. Most patients initially experience the insidious onset of chest pain or shortness of breath, and it rarely presents as spontaneous pneumothorax. CASE REPORTS: We report four patients who presented in this manner. Three of the patients were exposed to asbestos directly or indirectly at shipyards during World War II; the fourth was exposed as an insulator's wife. Two of our cases were not recognized to have MPM on histologic examination at first thoracotomy and remained asymptomatic for 12 and 22 months, respectively. In none of the patients described herein, was spontaneous pneumothorax the cause of death. CONCLUSIONS: Since many people were exposed to asbestos during and after World War II, spontaneous pneumothorax in a patient with the possibility of such exposure should raise the suspicion of malignant pleural mesothelioma. Copyright 2000 Wiley-Liss, Inc.
机译:背景:恶性胸膜间皮瘤(MPM)被认为是由排列在胸膜腔内的间皮细胞引起的。大多数患者最初会经历隐匿性的胸痛或呼吸急促发作,并且很少表现为自发性气胸。病例报告:我们报告了四名以这种方式出现的患者。第二次世界大战期间,其中三名患者直接或间接在船厂暴露于石棉之中;第四个人是绝缘子的妻子。我们的两个病例在首次开胸手术时经组织学检查未发现有MPM,分别保持12个月和22个月无症状。在本文所述的患者中,没有人是自发性气胸的死亡原因。结论:由于在第二次世界大战期间和之后,许多人接触了石棉,因此患者中自发性气胸并可能暴露于石棉,这应引起对恶性胸膜间皮瘤的怀疑。版权所有2000 Wiley-Liss,Inc.

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