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Vol. 12. Issue 5.
Pages 581-601 (September - October 2006)
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Vol. 12. Issue 5.
Pages 581-601 (September - October 2006)
Artigo de Revisão / Revision Article
Open Access
Pneumonias intersticiais idiopáticas – Uma revisão da literatura
Interstitial idiopathic pneumonias – A literature review
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Paulo José de Lima Mota1
1 Interno (5.º ano) do Internato Complementar de Pneumologia do Hospital de Pulido Valente, Lisboa.
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Resumo

As pneumonias intersticiais idiopáticas (PII) são um grupo de doenças de difícil estudo e abordagem clínica, devido a vários factores, dos quais se destacam a sua raridade e a enorme discrepância nas descrições dos achados clínicos, imagiológicos e histológicos pe-los vários autores. Um dos espelhos desta discrepância é o problema da classificação das várias entidades que constituem este grupo e que apenas em 2002 co-meçou a esboçar algum consenso entre as autorida-des na matéria.

O objectivo desta revisão é compilar a literatura mais relevante, de modo a facilitar a compreensão de um tema tão complexo.

Rev Port Pneumol 2006; XII (5): 581-601

Palavras-chave:
Pneumonias intersticiais idiopáticas
fibrose pulmonar idiopática
Abstract

Interstitial idiopathic pneumonias are a group of diseases whose rarity and variety of clinical, radiological and pathological descriptions creates difficulties in study and management. An example of this is the classification method for this group, with only 2002 seeing some consensus.

The aim of this article is to review the main literature to contribute to an understanding of this subject.

Rev Port Pneumol 2006; XII (5): 581-601

Key-words:
Interstitial idiopathic pneumonias
idiopathic pulmonary fibrosis
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Bibliografia
[1.]
M.J. Thomeer, et al.
Comparison of registries of interstitial lung diseases in three European countries.
Eur Respir J, 18 (2001), pp. 114s-118s
[2.]
J.H. Ryu, et al.
Idiopathic Pulmonary Fibrosis: Current Concepts.
Mayo Clin Proc, 73 (1998), pp. 1085-2001
[3.]
T.J. Gross, G.W. Hunninghake.
Idiopathic Pulmonary Fibrosis.
N Engl J Med, 345 (2001), pp. 517-525
[4.]
American Thoracic Society/European Respiratory Society International Multidisciplinary Consensus Classification of the Idiopathic Interstitial Pneumonias.
Am J Respir Crit Care Med, 165 (2002), pp. 277-304
[5.]
M. Harasawa, Y. Fukuchi, H. Morinari.
Interstitial pneumonia of unknown etiology, University of Tokyo Press, (1989),
[6.]
R.G. Crystal, J. Gadek, V. Ferrans.
Interstitial lung diseases: current concept of pathogenesis, staging and therapy.
Am J Med, 70 (1981), pp. 542-568
[7.]
L. Hamman, A.R. Rich.
Acute diffuse interstitial fibrosis of the lungs.
Bull Johns Hopkins Hosp, 74 (1944), pp. 177-212
[8.]
J. Olson, T.V. Colby, C.G. Elliott.
Hamman-Rich syndrome revisited.
Mayo Clin Proc, 65 (1990), pp. 1538-1548
[9.]
J.G. Scadding, K.F. Hinson.
Diffuse fibrosing alveolitis (diffuse interstitial fibrosis of the lungs): correlation of histology at biopsy with prognosis.
Thorax, 22 (1967), pp. 291-304
[10.]
A.A. Katzenstein, R.F. Fiorelli.
Nonspecific Interstitial Pneumonia/Fibrosis – Histologic Features and Clinical Significance.
Am J Surg Pathol, 18 (1994), pp. 136-147
[11.]
R.M. Du Bois, A.U. Wells.
Cryptogenic fibrosing alveo-litis/idiopathic pulmonary fibrosis.
Eur Respir J, 18 (2001), pp. 43s-55s
[12.]
C.B. Carrington, et al.
Natural history and treated course of usual and desquamative interstitial pneumonia.
N Engl J Med, 298 (1978), pp. 801-809
[13.]
A.G. Davison, et al.
Cryptogenic organizing pneumonitis.
Q J Med, 207 (1983), pp. 382-394
[14.]
J.L. Myers, et al.
Respiratory bronchiolitis causing interstitial lung disease. A clinicopathologic study of six cases.
Am Rev Respir Dis, 135 (1987), pp. 880-884
[15.]
A.L. Katzenstein, J.L. Myers.
Idiopathic Pulmonary Fi-brosis, clinical relevance of pathological classification.
Am J Respir Crit Care Med, 157 (1998), pp. 1301-1315
[16.]
G.R. Epler, et al.
Bronchiolitis obliterans organizing pneumonia.
N Engl J Med, 312 (1985), pp. 152-158
[17.]
J.F. Cordier.
Cryptogenic organizing pneumonitis.
Clin Chest Med, 14 (1993), pp. 677-692
[18.]
Idiopathic Pulmonary Fibrosis: Diagnosis and Treatment – International Consensus Statement.
Am J Respir Crit Care Med, 161 (2000), pp. 646-664
[19.]
G.M. Verleden, et al.
Genetic predisposition and patho-genetic mechanisms of interstitial lung diseases of unknown origin.
Eur Respir J, 18 (2001), pp. 17S-29S
[20.]
M. Demedts, et al.
Interstitial lung diseases: an epide-miological overview.
Eur Respir J, 18 (2001), pp. 2S-16S
[21.]
T.E. King, et al.
Idiopathic pulmonary fibrosis: diagnosis and treatment.
Am J Respir Crit Care Med, 161 (2000), pp. 646-664
[22.]
Z.D. Daniil, et al.
A histologic pattern of nonspecific interstitial pneumonia is associated with a better prognosis than usual interstitial pneumonia with cryptogenic fibrosing alveolitis.
Am J Respir Crit Care Med, 160 (1999), pp. 899-905
[23.]
T.E. King, R.L. Mortenson.
Cryptogenic organizing pneumonitis.
The North American experience. Chest, 102 (1992), pp. 8S-13S
[24.]
D. Moniz.
Pneumonias intersticiais idiopáticas – abordagem diagnóstica.
Rev Port Pneumol, VII (2001), pp. 386-392
[25.]
R. Ziesche, et al.
A preliminary study of long-term treatment with interferon gamma-1b and low-dose pred-nisolone in patients with idiopathic pulmonary fibrosis.
N Engl J Med, 341 (1999), pp. 1262-1269
[26.]
G. Raghu, et al.
A Placebo-Controlled Trial of Interferon Gamma-1b in Patients with Idiopathic Pulmonary Fibrosis.
N Engl J Med, 350 (2004), pp. 125-133
[27.]
T.E. King, et al.
Analyses of Efficacy End Points in a Controlled Trial of Interferon-γ 1b for Idiopathic Pulmonary Fibrosis.
Chest, 127 (2005), pp. 171-177
[28.]
International guidelines for the selection of lung transplant candidates.
Am J Respir Crit Care Med, 58 (1998), pp. 335-339
[29.]
J.A. Bjoraker, et al.
Prognostic significance of histopathologic subsets in idiopathic pulmonary fibrosis.
Am J Respir Crit Care Med, 157 (1998), pp. 199-203
[30.]
C.B. Carrington, et al.
Natural history and treated course of usual and desquamative interstitial pneumonia.
N Engl J Med, 298 (1978), pp. 801-809
Copyright © 2006. Sociedade Portuguesa de Pneumologia/SPP
Pulmonology
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