Literature DB >> 14769733

Prognostic implications of histologic patterns in multiple surgical lung biopsies from patients with idiopathic interstitial pneumonias.

Hannah Monaghan1, Athol U Wells, Thomas V Colby, Roland M du Bois, David M Hansell, Andrew G Nicholson.   

Abstract

STUDY
OBJECTIVES: To determine the prevalence and prognostic significance of histologic discordance in multiple lung biopsy specimens obtained from patients investigated for suspected cryptogenic fibrosing alveolitis (CFA)/idiopathic pulmonary fibrosis (IPF).
METHODS: and results: Between 1984 and 2001, 64 patients undergoing investigation for CFA/IPF were identified in whom multiple biopsies were performed that showed either a pattern of usual interstitial pneumonia (UIP) or nonspecific interstitial pneumonia (NSIP). These cases were classified into three groups: concordant UIP-UIP (n = 25, 39.1%), discordant UIP-NSIP (n = 8,12.5%), and concordant NSIP-NSIP (n = 31, 48.4%). The discordant UIP group had survival, clinical, and physiologic features similar to those of the concordant UIP group, and prognosis in both concordant and discordant UIP groups was significantly worse than that of the concordant NSIP group (p = 0.02 and p = 0.04, respectively). The age of the concordant UIP group was higher than that of the concordant NSIP group, with the mean age of the discordant group being intermediate. There were no significant differences among the three groups in smoking history, duration of dyspnea, presence or absence of crackles, FVC, diffusion capacity of the lung for carbon monoxide, or PaO(2).
CONCLUSIONS: Patients with discordant UIP-NSIP results on multiple biopsies show clinical behavior similar to those with concordant UIP-UIP and should be regarded as having CFA/IPF in the correct clinical context, rather than "idiopathic NSIP" for the purposes of management. Multiple biopsies should be considered in all patients in order to improve the prognostic information provided by lung biopsy.

Entities:  

Mesh:

Year:  2004        PMID: 14769733     DOI: 10.1378/chest.125.2.522

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  29 in total

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Review 2.  [Idiopathic interstitial pneumonias: from classification to diagnostic work-up].

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Journal:  Radiologe       Date:  2007-05       Impact factor: 0.635

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4.  Idiopathic or connective tissue disease-associated interstitial lung disease: a case of HRCT mimicry.

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Review 6.  Classification and natural history of the idiopathic interstitial pneumonias.

Authors:  Dong Soon Kim; Harold R Collard; Talmadge E King
Journal:  Proc Am Thorac Soc       Date:  2006-06

7.  Bone Marrow-Derived Cells in the Pathogenesis of Lung Fibrosis.

Authors:  Bethany B Moore; Victor J Thannickal; Galen B Toews
Journal:  Curr Respir Med Rev       Date:  2005

8.  Interstitial Lung Disease Associated with Connective Tissue Diseases.

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9.  Diffuse alveolar hemorrhage in coumarin users: a fibrosing interstitial pneumonia trigger?

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Review 10.  Animal models of fibrotic lung disease.

Authors:  Bethany B Moore; William E Lawson; Tim D Oury; Thomas H Sisson; Krishnan Raghavendran; Cory M Hogaboam
Journal:  Am J Respir Cell Mol Biol       Date:  2013-08       Impact factor: 6.914

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