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Acute pulmonary edema, capillaritis and alveolar hemorrhage: pulmonary manifestations coexistent in antiphospholipid syndrome and systemic lupus erythematosus?

机译:急性肺水肿,毛细血管炎和肺泡出血:抗磷脂综合征和系统性红斑狼疮并存肺部表现?

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Pulmonary capillaritis and alveolar hemorrhage are rare yet serious and life threatening complications of systemic lupus erythematosus (SLE). Pulmonary manifestations of antiphospholipid syndrome (APS) are similar and include, apart from pulmonary embolism and pulmonary hypertension, pulmonary capillaritis, diffuse alveolar hemorrhage and respiratory insufficiency in patients with catastrophic APS. Herein, we described the radiological features of three patients with pulmonary and SLE-associated APS, manifested with pulmonary edema, capillaritis and alveolar hemorrhage. We observed that the radiological features of pulmonary APS shared close resemblance to those of pulmonary SLE. Based on these findings, we conclude that both entities are not only histologically, but also radiologically indistinguishable from each other, suggesting a mutual pathogenetic mechanism. This raises the question of whether some of the reported lupus pneumonitis cases in the past might be manifestations of APS rather than of SLE.
机译:肺毛细血管炎和肺泡出血很少见,但很严重,严重威胁着系统性红斑狼疮(SLE)的生命。抗磷脂综合征(APS)的肺部表现相似,除了肺栓塞和肺动脉高压外,灾难性APS患者的肺毛细血管炎,弥漫性肺泡出血和呼吸功能不全。在此,我们描述了三例肺和SLE相关的APS患者的放射学特征,表现为肺水肿,毛细血管炎和肺泡出血。我们观察到,肺部APS的放射学特征与肺部SLE的放射学特征非常相似。基于这些发现,我们得出结论,这两个实体不仅在组织学上而且在放射学上彼此之间没有区别,表明了相互的致病机制。这就提出了一个问题,即过去报道的某些狼疮性肺炎病例是否可能是APS而非SLE的表现。

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