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首页> 外文期刊>Leukemia and lymphoma >Myelofibrosis after essential thrombocythemia complicated by alveolar proteinosis.
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Myelofibrosis after essential thrombocythemia complicated by alveolar proteinosis.

机译:原发性血小板增多症后并发肺泡蛋白沉着症的骨髓纤维化。

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摘要

Hematological diseases are often accompanied by respiratory disorders. Pulmonary alveolar proteinosis (PAP) is a rare disease characterized by excessive accumulation of surfactant in the alveolar space. We describe a case of PAP complicated by myelofibrosis following essential thrombocythemia. The patient developed high fever, respiratory failure, and leuko-erythroblastosis during the progressive course of PAP. These symptoms were alleviated by prednisolone. The level of serum IL-6 was elevated when PAP was progressing rapidly. This may explain why the symptoms were alleviated by the steroids.
机译:血液疾病常伴有呼吸系统疾病。肺泡蛋白沉着症(PAP)是一种罕见的疾病,其特征在于肺泡空间中表面活性剂的过度积累。我们描述了在原发性血小板增多症后并发骨髓纤维化的PAP病例。患者在PAP的进行过程中出现高烧,呼吸衰竭和白细胞成纤维细胞增多。泼尼松龙可缓解这些症状。当PAP快速发展时,血清IL-6水平升高。这可以解释为什么类固醇可以缓解症状。

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