Virginia-Maryland College of Veterinary Medicine, Blacksburg, VA.
Virginia Department of Agriculture and Consumer Services, Harrisonburg, VA.
Vet Pathol. 2022 Jul;59(4):586-601. doi: 10.1177/03009858221082228. Epub 2022 Mar 6.
Classification of pneumonia in animals has been controversial, and the most problematic pattern is interstitial pneumonia. This is true from the gross and histologic perspectives, and also from a mechanistic point of view. Multiple infectious and noninfectious diseases are associated with interstitial pneumonia, all of them converging in the release of inflammatory mediators that generate local damage and attract inflammatory cells that inevitably trigger a second wave of damage. Diffuse alveolar damage is one of the more frequently identified histologic types of interstitial pneumonia and involves injury to alveolar epithelial and/or endothelial cells, with 3 distinct stages. The first is the "exudative" stage, with alveolar edema and hyaline membranes. The second is the "proliferative" stage, with hyperplasia and reactive atypia of type II pneumocytes, infiltration of lymphocytes, plasma cells, and macrophages in the interstitium and early proliferation of fibroblasts. These stages are reversible and often nonfatal. If damage persists, there is a third "fibrosing" stage, characterized by fibrosis of the interstitium due to proliferation of fibroblasts/myofibroblasts, persistence of type II pneumocytes, segments of squamous metaplasia of alveolar epithelium, plus inflammation. Understanding the lesion patterns associated with interstitial pneumonias, their causes, and the underlying mechanisms aid in accurate diagnosis that involves an interdisciplinary collaborative approach involving pathologists, clinicians, and radiologists.
动物肺炎的分类一直存在争议,最具问题性的模式是间质性肺炎。从大体和组织学的角度来看,从发病机制的角度来看,情况确实如此。多种感染性和非传染性疾病与间质性肺炎有关,所有这些疾病都集中在释放炎症介质上,这些炎症介质会产生局部损伤,并吸引炎症细胞,从而不可避免地引发第二波损伤。弥漫性肺泡损伤是间质性肺炎中较常识别的组织学类型之一,涉及肺泡上皮和/或内皮细胞的损伤,具有 3 个不同阶段。第一个阶段是“渗出性”阶段,肺泡水肿和透明膜形成。第二个阶段是“增殖性”阶段,II 型肺泡细胞增生和反应性异型增生,间质中淋巴细胞、浆细胞和巨噬细胞浸润,以及早期成纤维细胞增殖。这些阶段是可逆的,通常不会致命。如果损伤持续存在,则进入第三个“纤维化”阶段,特征为间质纤维化,原因是成纤维细胞/肌成纤维细胞增殖、II 型肺泡细胞持续存在、肺泡上皮的鳞状化生段以及炎症。了解与间质性肺炎相关的病变模式、其病因和潜在机制有助于进行准确的诊断,这需要病理学家、临床医生和放射科医生进行跨学科合作。