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胸部疾病中的假象:间质性混浊。

Mimics in chest disease: interstitial opacities.

机构信息

Department of Radiology, University Hospital of Alexandroupolis, Democritus University of Thrace, Dragana, 68100, Alexandroupolis, Greece,

出版信息

Insights Imaging. 2013 Feb;4(1):9-27. doi: 10.1007/s13244-012-0207-7. Epub 2012 Dec 18.

Abstract

Septal, reticular, nodular, reticulonodular, ground-glass, crazy paving, cystic, ground-glass with reticular, cystic with ground-glass, decreased and mosaic attenuation pattern characterise interstitial lung diseases on high-resolution computed tomography (HRCT). Occasionally different entities mimic each other, either because they share identical HRCT findings or because of superimposition of patterns. Idiopathic pulmonary fibrosis (IPF), fibrosis associated with connective tissue disease, asbestosis, end-stage sarcoidosis or chronic hypersensitivity pneumonitis (HP) may present with lower zone, subpleural reticular pattern associated with honeycombing. Lymphangiomyomatosis may be indistinguishable from histiocytosis or extensive emphysema. Both pulmonary oedema and lymphangitic carcinomatosis may be characterised by septal pattern resulting from thickened interlobular septa. Ill-defined centrilobular nodular pattern may be identically present in HP and respiratory bronchiolitis-associated with interstitial lung disease (RBILD). Sarcoidosis may mimic miliary tuberculosis or haematogenous metastases presenting with miliary pattern, while endobronchial spread of tuberculosis may be indistinguishable from panbronchiolitis, both presenting with tree-in-bud pattern. Atypical infection presenting with ground-glass mimics haemorrhage. Ground-glass pattern with minimal reticulation is seen in desquamative interstitial pneumonia (DIP), RBILD and non-specific interstitial pneumonia (NSIP). Obliterative bronchiolitis and panlobular emphysema may present with decreased attenuation pattern, while obliterative bronchiolitis, chronic pulmonary embolism and HP may manifest with mosaic attenuation pattern. Various mimics in interstitial lung diseases exist. Differential diagnosis is narrowed based on integration of predominant HRCT pattern and clinical history. Teaching Points • To learn about the different HRCT patterns, which are related to interstitial lung diseases. • To be familiar with the more "classical" entities presenting with each HRCT pattern. • To discuss possible overlap of different HRCT patterns and the more common mimics in each case. • To learn about some clues that help differentiate the various diagnostic mimics on HRCT.

摘要

肺间质疾病在高分辨率 CT(HRCT)上的表现为间隔、网状、结节状、网状结节状、磨玻璃、鹅卵石、囊性、磨玻璃伴网状、囊性伴磨玻璃、衰减减少和马赛克。偶尔不同的实体彼此相似,要么是因为它们具有相同的 HRCT 发现,要么是因为模式的叠加。特发性肺纤维化(IPF)、结缔组织疾病相关纤维化、石棉肺、终末期结节病或慢性过敏性肺炎(HP)可能表现为下区、胸膜下网状模式伴蜂窝肺。淋巴管肌瘤病可能与组织细胞增多症或广泛肺气肿无法区分。肺充血和淋巴管癌病都可能表现为增厚的小叶间隔导致的间隔模式。边界不清的中心小叶结节模式可能在 HP 和与间质性肺病相关的呼吸细支气管炎(RBILD)中同样存在。结节病可能模拟血源性转移的粟粒性肺结核,表现为粟粒性模式,而肺结核的支气管内播散与 panbronchiolitis 无法区分,两者都表现为树芽征。表现为磨玻璃影的不典型感染类似于出血。脱屑性间质性肺炎(DIP)、RBILD 和非特异性间质性肺炎(NSIP)可见最小程度的网状磨玻璃影。闭塞性细支气管炎和全小叶肺气肿可能表现为衰减减少模式,而闭塞性细支气管炎、慢性肺栓塞和 HP 可能表现为马赛克衰减模式。肺间质疾病存在各种类似物。基于主要 HRCT 模式和临床病史的综合,鉴别诊断范围缩小。教学要点 • 了解与肺间质疾病相关的不同 HRCT 模式。 • 熟悉每种 HRCT 模式表现的更“经典”实体。 • 讨论不同 HRCT 模式的重叠以及每种情况下更常见的类似物。 • 了解有助于在 HRCT 上区分各种诊断类似物的一些线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d143/3579994/a117a7eadf4a/13244_2012_207_Fig1_HTML.jpg

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