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Malignant pleural mesothelioma in a child with ataxia-telangiectasia

机译:小儿共济失调毛细血管扩张性恶性胸膜间皮瘤

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摘要

Ataxia-telangiectasia (AT) is a hereditary disorder characterized by progressive neurological dysfunction, oculocutaneous telangiectasia, immunodeficiency, cancer susceptibility, and radiation sensitivity. Pleural neoplasms are extremely rare in the pediatric population, even in patients with AT. We describe the case of a 16-year-old male with AT who developed a malignant pleural mesothelioma (MPM). Benign or infectious lung and pleural diseases are common in those with AT. Hence, delayed diagnosis of respiratory neoplasms can occur in these patients. This report highlights the need of heightened vigilance in patients with AT with recurrent or persistent pleuropulmonary disease. To our knowledge, no other cases of MPM in children with AT have been reported.
机译:共济失调毛细血管扩张症(AT)是一种遗传性疾病,其特征是进行性神经功能障碍,眼皮肤毛细血管扩张,免疫缺陷,癌症易感性和放射敏感性。即使在患有AT的患者中,胸膜肿瘤在儿科人群中也极为罕见。我们描述了一个16岁的男性,患有AT的病例,该男性发生了恶性胸膜间皮瘤(MPM)。良性或感染性肺和胸膜疾病常见于AT患者。因此,这些患者可能会出现呼吸道肿瘤的延迟诊断。该报告强调了患有复发性或持续性胸膜肺疾病的AT患者需要提高警惕。据我们所知,尚无AT儿童患MPM的其他报道。

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