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Malignant pleural mesothelioma presenting as a spontaneous pneumothorax

机译:恶性胸膜间皮瘤表现为自发性气胸

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AbstractMalignant 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 have a history of asbestos exposure. MPM rarely presents as spontaneous pneumothorax. We report two male patients who presented with a spontaneous hydropneumothorax. One was exposed to asbestos and the other was not. Computed tomography showed tiny nodules with pleural thickness. They both underwent pleural effusion cytology and/or pleural biopsy. Therefore, the pathological diagnosis of MPM was obtained in both cases. We also reviewed 16 Japanese MPM cases with pneumothorax including our two patients. More than half of the patients suffered from pneumothorax repeatedly. We emphasize the need to obtain a pathological diagnosis of pleural effusion cytology and/or pleural biopsy in older patients presenting with a spontaneous hydropneumothorax.
机译:摘要恶性胸膜间皮瘤(MPM)被认为是由排列在胸膜腔中的间皮细胞引起的。大多数患者最初会经历隐匿性的胸痛或呼吸急促发作,并且有接触石棉的病史。 MPM很少表现为自发性气胸。我们报告了两名男性患者自发性气胸。一个暴露于石棉,另一个暴露于石棉。计算机体层摄影术显示小结节具有胸膜厚度。他们都接受了胸腔积液细胞学检查和/或胸膜活检。因此,在两种情况下均获得了MPM的病理诊断。我们还回顾了16例日本MPM气胸患者,其中包括2例患者。超过一半的患者反复患有气胸。我们强调需要对患有自发性水气胸的老年患者进行胸腔积液细胞学和/或胸膜活检的病理诊断。

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