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Isolated pulmonary mucormycosis in an immunocompetent patient: a case report and systematic review of the literature

机译:免疫因职患者的分离的肺粘膜病:文献的案例报告和系统审查

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Pulmonary mucormycosis caused by Mucorales is a highly lethal invasive fungal infection usually found in immunocompromised patients. Isolated pulmonary mucormycosis in immunocompetent patients is very rare. Here, we present a case of a 32-year-old male who developed pulmonary mucormycosis without any known immunodeficiency. The patient presented to our hospital because of cough and chest pain along with blood in the sputum. He was first treated for community-acquired pneumonia until bronchoalveolar lavage fluid culture confirmed the growth of Absidia. His symptoms were relieved with the use of amphotericin B, and he eventually recovered. We also provide a systematic review of relevant literature to summarize the characteristics of pulmonary mucormycosis in immunocompetent patients. Pulmonary mucormycosis has variable clinical presentations and is difficult to identify. Due to its high fatality rate, clinicians should make judgements regarding suspected cases correctly and in a timely manner to avoid misdiagnosis and delayed treatment.
机译:粘液引起的肺粘膜霉菌是一种高度致命的侵袭性真菌感染,通常在免疫疗效中发现。孤立的肺粘膜粘膜粘膜霉菌在免疫功能性患者中非常罕见。在这里,我们提出了一个32岁的男性,在没有任何已知的免疫缺陷的情况下开发了肺粘膜霉菌症。由于咳嗽和胸部疼痛以及痰中的血液,患者呈现给我们的医院。他首先对社区获得的肺炎治疗,直至支气管肺泡灌洗液培养培养确认了吸收的生长。使用两性霉素B,他的症状得到了缓解,他最终恢复。我们还提供了对相关文献的系统审查,总结了免疫活性患者肺粘膜霉菌的特征。肺粘膜粘性症具有可变的临床介绍,并且难以识别。由于其高死亡率,临床医生应当正确地对涉嫌病例进行判断,并及时避免误诊和延迟治疗。

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