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肺孤立性坏死性肉芽肿:鉴别特征与病因

Solitary necrotizing granulomas of the lung: differentiating features and etiology.

作者信息

Ulbright T M, Katzenstein A L

出版信息

Am J Surg Pathol. 1980 Feb;4(1):13-28.

PMID:7361992
Abstract

The clinical and pathologic features of 86 roentgenographically solitary pulmonary granulomas were reviewed to determine etiology and to provide guidelines for histologic evaluation. Fungal or acid-fast organisms were identified within the tissue in 60 cases (70%) and fragments of a helminth were found in one. The organisms were almost always present in the center of necrotic granulomas, and examination of two blocks containing active granulomas was usually sufficient for their identification. Microbiological cultures were less productive than direct examination of the tissue. In 25 cases an infectious etiology could not be identified: two were diagnosed as hyalinizing granuloma, one as Wegener's granulomatosis, and 22 were not further classified. A prominent overlapping spectrum of histologic features was found between infectious granulomas and Wegener's granulomatosis, suggesting that the latter may represent an abnormal immune response to an infectious agent that is no longer identifiable within the tissue. Caution is urged in diagnosing limited Wegener's granulomatosis and other pulmonary angiitides in patients with roentgenographically solitary granulomas.

摘要

回顾了86例X线表现为孤立性肺肉芽肿的临床和病理特征,以确定病因并为组织学评估提供指导。60例(70%)组织中发现真菌或抗酸菌,1例发现蠕虫碎片。这些微生物几乎总是存在于坏死性肉芽肿的中心,检查两块含有活动性肉芽肿的组织通常足以识别它们。微生物培养的阳性率低于组织直接检查。25例无法确定感染病因:2例诊断为透明变性肉芽肿,1例诊断为韦格纳肉芽肿,22例未进一步分类。在感染性肉芽肿和韦格纳肉芽肿之间发现了显著的组织学特征重叠谱,提示后者可能代表对组织内无法再识别的感染因子的异常免疫反应。对于X线表现为孤立性肉芽肿的患者,在诊断局限性韦格纳肉芽肿和其他肺血管炎时应谨慎。

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