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Multidisciplinary Approach to Hypersensitivity Pneumonitis
被引:39
|作者:
Elicker, Brett M.
[1
]
Jones, Kirk D.
[2
]
Henry, Travis S.
[4
]
Collard, Harold R.
[3
]
机构:
[1] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, 505 Parnassus Ave,Box 0628, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Internal Med, San Francisco, CA 94143 USA
[4] Emory Univ, Sch Med, Dept Radiol & Imaging Sci, Atlanta, GA USA
关键词:
diffuse lung disease;
idiopathic pulmonary fibrosis;
hypersensitivity pneumonitis;
interstitial lung disease;
IDIOPATHIC PULMONARY-FIBROSIS;
RESOLUTION COMPUTED-TOMOGRAPHY;
INTERSTITIAL LUNG-DISEASE;
BRONCHOALVEOLAR LAVAGE;
ACUTE EXACERBATIONS;
DIAGNOSTIC YIELD;
CT;
SURVIVAL;
CLASSIFICATION;
PATTERNS;
D O I:
10.1097/RTI.0000000000000186
中图分类号:
R8 [特种医学];
R445 [影像诊断学];
学科分类号:
1002 ;
100207 ;
1009 ;
摘要:
Hypersensitivity pneumonitis (HP) may be a challenging diagnosis given the wide variability of its clinical, radiographic, and pathologic manifestations. A multidisciplinary approach to diagnosis is critical in maintaining a high specificity for HP. An in-depth knowledge of all 3 arms of the multidisciplinary approach helps clinicians, radiologists, and pathologists interpret their own findings in the context of the entire presentation. In some cases, the combination of clinical findings (ie, an identifiable exposure) and typical findings on high-resolution computed tomography is considered diagnostic of HP, and pathologic confirmation is not necessary. As many as 50% of patients do not have a clear exposure, however. These patients may be difficult to distinguish from idiopathic disorders. In these cases, high-resolution computed tomography and pathology are the primary data points that may suggest the correct diagnosis. The goal of this paper is to discuss recent advances in HP and to present the spectrum of clinical, radiographic, and pathologic findings.
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页码:92 / 103
页数:12
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