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Cryptogenic organizing pneumonia

机译:隐源性组织性肺炎

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摘要

Organizing pneumonia (OP) is a pathological pattern defined by the characteristic presence of buds of granulation tissue within the lumen of distal pulmonary airspaces consisting of fibroblasts and myofibroblasts intermixed with loose connective matrix. This pattern is the hallmark of a clinical pathological entity, namely cryptogenic organizing pneumonia (COP) when no cause or etiologic context is found. The process of intraalveolar organization results from a sequence of alveolar injury, alveolar deposition of fibrin, and colonization of fibrin with proliferating fibroblasts. A tremendous challenge for research is represented by the analysis of features that differentiate the reversible process of OP from that of fibroblastic foci driving irreversible fibrosis in usual interstitial pneumonia because they may determine the different outcomes of COP and idiopathic pulmonary fibrosis (IPF), respectively. Three main imaging patterns of COP have been described: (1) multiple patchy alveolar opacities (typical pattern), (2) solitary focal nodule or mass (focal pattern), and (3) diffuse infiltrative opacities, although several other uncommon patterns have been reported, especially the reversed halo sign (atoll sign). Definitive diagnosis is based on (1) a suggestive clinical radiological presentation, (2) the demonstration of the characteristic pathological pattern at lung histopathology, and (3) exclusion of possible causes. Transbronchial biopsies or a transthoracic biopsy may also contribute to the pathological diagnosis. Rapid clinical and imaging improvement is obtained with corticosteroid therapy. Because of the risk of misdiagnosing alternative conditions that may mimic OP, only typical cases may be managed without histopathological confirmation, and patients should be followed with particular attention paid to any clue of alternate diagnosis, especially in case of incomplete response to treatment. Patients and clinicians must be aware of frequent relapses after stopping corticosteroid treatment.
机译:组织性肺炎(OP)是一种病理模式,其特征是远端肺空域管腔内肉芽组织芽的特征性存在,其由成纤维细胞和成肌纤维细胞与疏松结缔组织混合而成。这种模式是临床病理实体的标志,即未发现原因或病因的情况下的隐源性组织性肺炎(COP)。肺泡内组织的过程是由一系列的肺泡损伤,纤维蛋白的肺泡沉积以及纤维蛋白在增殖性成纤维细胞中定植而引起的。在正常的间质性肺炎中,将OP的可逆过程与驱动不可逆性纤维化的成纤维细胞灶的可逆过程区分开来的特征分析,代表着研究的巨大挑战,因为它们可能分别确定COP和特发性肺纤维化(IPF)的不同结果。 COP的三种主要成像模式已被描述:(1)多个斑块状肺泡混浊(典型模式),(2)孤立性局灶性结节或肿块(局部模式)和(3)弥漫性浸润性混浊,尽管已经发现了其他几种罕见的模式报告,特别是反转的晕轮符号(环礁符号)。明确的诊断基于(1)提示性临床放射学表现,(2)肺组织病理学特征性病理模式的证实以及(3)排除可能的原因。经支气管活检或经胸活检也可能有助于病理诊断。皮质类固醇疗法可实现快速的临床和影像学改善。由于可能会误诊可能模仿OP的其他疾病,因此只有在没有组织病理学证实的情况下才可以治疗典型病例,并且应特别注意患者的其他诊断线索,尤其是对治疗反应不完全的情况。患者和临床医生必须注意停止糖皮质激素治疗后经常复发。

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