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Diffuse Alveolar Hemorrhage and Pulmonary Vasculitides: Histopathologic Findings

机译:弥漫性肺泡出血和肺血管素:组织病理学发现

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Vasculitides are a heterogeneous group of disorders in which inflammation of blood vessel walls is present at least some time during the course of the disease. Vasculitides can affect any caliber or type of vessel in many anatomic sites; however, the disease can alter more than just vasculature. Given the diversity of vasculitides, in 2012, a revised classification system was proposed to categorize vasculitides by the type of vessel involved includingsize, function, and structural attributes. In the lung, vasculitis impacts both the pulmonary vessels and parenchyma. Extrapulmonary involvement, particularly with concomitant kidney involvement, is a frequent occurrence. Pulmonary vasculitides often present with hemoptysis, pathologically manifested as diffuse alveolar hemorrhage (DAH) with or without capillaritis and can be life threatening when diffuse throughout the lungs. Etiologies for DAH include both primary and secondary vasculitides, along with collagen-vascular diseases, infection, and drug toxicity. Therefore, diagnosing the specific vasculitic etiology often relies on comprehensive assessment of all clinical, laboratory/serological, imaging, and histopathologic features that may be present. The most common primary pulmonary vasculitides often affect small vessels and are associated with circulating antineutrophilic cytoplasmic antibodies (ANCAs). In the 2012 classification, these include granulomatosis with polyangiitis (formerly Wegener granulomatosis), eosinophilic granulomatosis with polyangiitis (formerly Churg-Strauss' syndrome), and microscopic polyangiitis. Other less frequent vasculitides that are non-ANCA associated or affect medium-to large-sized vessels can have pulmonary involvement. These entities are usually associated with extrapulmonary disease and include polyarteritis nodosa, Takayasu's arteritis, Behcet's disease, and antibasement membrane antibody disease (formerly Goodpasture's syndrome). Although all vasculitides have vessel wall inflammation at some phase in the disease process, their histopathologic findings are as diverse as the group of diseases themselves. The characteristic histologic findings of the pulmonary vasculitides will be reviewed here.
机译:血管素是一种异质的疾病组,其中血管壁的炎症在疾病过程中至少存在一段时间。血管素可以影响许多解剖部位中的任何口径或类型的血管;然而,这种疾病可以改变超过血管系统。鉴于血管素的多样性,2012年,提出了经修订的分类系统,通过涉及,功能和结构属性的船舶的类型分类血管项。在肺中,血管炎均对肺部血管和实质造成的影响。尤其是伴随的肾受累,常见的肾脏受累是经常发生的。肺血管素通常存在于咯血,病理上表现为弥漫性肺泡出血(DAH),有或没有毛细血管炎,并且在整个肺部扩散时可能是危及的。 DAH的病因包括初级和二级血管素,以及胶原血管疾病,感染和药物毒性。因此,诊断特定的血管病病程通常依赖于可能存在的所有临床,实验室/血清学,成像和组织病理学特征的综合评估。最常见的主要肺血管素通常会影响小血管,并且与循环抗胸腺细胞质抗体(ANCAS)相关。在2012年分类中,这些包括肉芽肿病,具有多炔炎(以前Wegener肉芽肿),嗜酸性粒细胞芽孢杆菌病,具有多锰炎(以前的Churg-Strauss'综合征)和微观的多阳炎。其他较少频繁的血管素,其是非ANCA相关或影响培养基的大型血管可以具有肺部受累。这些实体通常与外肺疾病有关,包括多性炎症,高山的动脉炎,Behcet疾病和抗体膜抗体疾病(以前的好福尔本综合症)。虽然所有血管素在疾病过程中具有某种阶段的血管壁炎症,但它们的组织病理学发现与一组疾病本身一样多样化。将在此进行审查肺血管素的特征组织学发现。

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