Nonspecific interstitial pneumonia: pathologic features and clinical implications

被引:7
|
作者
Myers, Jeffrey L. [1 ]
机构
[1] Univ Michigan, Div Anat Pathol, Ann Arbor, MI 48109 USA
关键词
idiopathic interstitial; pneumonia; pulmonary fibrosis; diffuse interstitial lung disease; lung biopsy; IDIOPATHIC PULMONARY-FIBROSIS; HIGH-RESOLUTION CT; HYPERSENSITIVITY PNEUMONITIS; PROGNOSTIC-SIGNIFICANCE; HISTOLOGIC PATTERN; SURVIVAL; ALVEOLITIS; CLASSIFICATION; DIAGNOSIS; BIOPSY;
D O I
10.1053/j.semdp.2007.06.004
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Nonspecific interstitial pneumonia (NSIP) is a form of chronic interstitial pneumonia that should be separated from the other idiopathic interstitial pneumonias, including most importantly, usual interstitial pneumonia (UIP). Diagnosis is predicated on identification of characteristic findings in a surgical lung biopsy in the appropriate clinical and radiological context. Affected patients may have a variety of underlying or associated conditions, although most have a form of idiopathic lung disease associated with a more favorable prognosis than UIP/idiopathic pulmonary fibrosis (IPF). Keys to distinguishing NSIP from UIP include absence of heterogeneous lung involvement, architectural distortion in the form of fibrotic scar-ring and/or honeycomb change, and fibroblast foci in NSIP. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:183 / 187
页数:5
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