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肺结核的CT与病理学相关性

CT-pathology correlation of pulmonary tuberculosis.

作者信息

Im J G, Itoh H, Lee K S, Han M C

机构信息

Department of Radiology, Seoul National University College of Medicine, Korea.

出版信息

Crit Rev Diagn Imaging. 1995;36(3):227-85.

PMID:7546270
Abstract

Pulmonary tuberculosis is a chronic granulomatous disease characterized radiologically by nodules, air-space consolidation, propensity for cavitation, and calcification, and pathologically by caseating granulomas or pneumonia, and a great propensity for fibrosis and dystrophic calcification. Primary tuberculosis typically appears as air-space consolidation with hilar or mediastinal lymphadenitis. Postprimary tuberculosis appears most commonly as nodular and linear opacities at the lung apex. CT findings of early bronchogenic spread of postprimary tuberculosis are centrilobular 2- to 4-mm nodules or branching linear structure, 5- to 8-mm poorly defined nodules, lobular consolidation, cavities, and thickening of interlobular septa. Centrilobular nodules or branching linear lesions and poorly defined nodules on CT scan correspond to caseation materials filling the bronchioles, and centrilobular air-space consolidation with caseation necrosis. Poorly defined nodule or lobular consolidation usually consists of central caseation necrosis and peripheral nonspecific inflammation. Cavitation usually occurs at the centrilobular area and may progress to a larger coalescent cavity. With antituberculous therapy, resolution typically occurs from the peripheral portion of the poorly defined nodule or lobular consolidation and results in varying degrees of fibrous bands, bronchovascular distortion, emphysema, and bronchiectasis. Miliary tuberculosis appears as well-defined randomly distributed nodules on CT scan that correspond with nodules consisting of central caseation necrosis and peripheral epitheloid and fibrous tissue. Analysis of CT images on the basis of pathologic correlation is helpful in understanding the morphology of pulmonary tuberculosis.

摘要

肺结核是一种慢性肉芽肿性疾病,其放射学特征为结节、实变、易形成空洞和钙化,病理学特征为干酪样肉芽肿或肺炎,且极易发生纤维化和营养不良性钙化。原发性肺结核通常表现为实变伴肺门或纵隔淋巴结炎。继发性肺结核最常见的表现是肺尖部的结节状和条索状阴影。继发性肺结核早期支气管播散的CT表现为小叶中心2~4mm的结节或分支状线性结构、5~8mm边界不清的结节、小叶实变、空洞及小叶间隔增厚。CT上的小叶中心结节或分支状线性病灶以及边界不清的结节对应于细支气管内充满干酪样物质,以及小叶中心实变伴干酪样坏死。边界不清的结节或小叶实变通常由中央干酪样坏死和周围非特异性炎症组成。空洞通常发生在小叶中心区域,可进展为更大的融合性空洞。经过抗结核治疗,通常从边界不清的结节或小叶实变的周边部分开始吸收,导致不同程度的纤维条索、支气管血管扭曲、肺气肿和支气管扩张。粟粒性肺结核在CT上表现为边界清晰、随机分布的结节,与由中央干酪样坏死及周围上皮样和纤维组织构成的结节相对应。基于病理相关性分析CT图像有助于理解肺结核的形态。

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