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Respiratory bronchiolitis-associated interstitial lung disease with fibrosis is a lesion distinct from fibrotic nonspecific interstitial pneumonia: a proposal

机译:呼吸性细支气管炎相关的间质性肺疾病伴纤维化是一种不同于纤维化非特异性间质性肺炎的病变:

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Nine cases of clinical and radiographic chronic interstitial lung disease are presented that have features of respiratory bronchiolitis-associated interstitial lung disease, but were associated with a respiratory bronchiolitis having extensive paucicellular lamellar eosinophilic collagenous thickening of alveolar septa in a patchy, particularly subpleural distribution. Patients were middle-aged with shortness of breath, mixed obstructive and restrictive lung disease with markedly reduced diffusing capacity and radiographs demonstrating centrilobular micronodules, occasional ground glass opacities and emphysema. All were alive at follow-up. The morphology of this process raises the differential diagnosis with the fibrotic form of nonspecific interstitial pneumonia and highlights the role of cigarette smoking as a potential cause of fibrotic lung disease.
机译:提出了9例临床和放射学上的慢性间质性肺病病例,这些病例具有呼吸性细支气管炎相关的间质性肺病的特征,但与呼吸性细支气管炎有关,该细支气管肺泡的薄层状,特别是胸膜下分布的肺泡间隔广泛嗜酸性粒细胞性胶原增厚。患者为中年人,呼吸急促,混合性阻塞性和限制性肺疾病,扩散能力明显降低,X线片显示小叶小结节,偶有毛玻璃样混浊和肺气肿。所有人都还活着。该过程的形态提高了非特异性间质性肺炎的纤维化形式的鉴别诊断,并强调了吸烟是纤维化性肺病的潜在原因。

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