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Acute Exacerbation of Pleuroparenchymal Fibroelastosis Secondary to Allogenic Hematopoietic Stem Cell Transplantation

机译:继发性造血干细胞移植继承的急性强硬肌肌慢性

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In this article, we report a case with pleuroparenchymal fibroelastosis (PPFE) following hematopoietic stem cell transplantation (HSCT) that developed acute respiratory failure with new bilateral ground glass opacity, which could not be explained by either a pulmonary infection, drug toxicity or extraparenchymal causes. Although combination therapy with multiple immunosuppressants was transiently effective, the patient died from a recurrent exacerbation. Autopsied lungs demonstrated diffuse alveolar damage superimposed on PPFE. There was no evidence of any coexisting interstitial pneumonia with the usual interstitial pneumonia (UIP) pattern. Our case suggests that acute exacerbation can occur in patients with post-HSCT PPFE, even when a coexisting UIP pattern is absent.
机译:在本文中,我们报告了血管发育性干细胞移植(HSCT)后患有胸膜间充感肌肉菌(PPFE)的案例,其产生急性呼吸衰竭,其具有新的双侧覆盖玻璃不透明度,这无法通过肺部感染,药物毒性或印刷原因来解释。虽然多种免疫抑制剂的联合治疗瞬时有效,但患者从复发性加剧中死亡。尸检肺叠加在PPFE上叠加的弥漫性肺泡损伤。没有证据表明任何带有常用的间质肺炎(UIP)模式的患有间质肺炎。我们的病例表明,即使不存在共存UIP模式,患者患者患者可能发生急性加剧。

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