Nonspecific interstitial pneumonia

被引:31
作者
Flaherty, Kevin R. [1 ]
Martinez, Fernando J. [1 ]
机构
[1] Univ Michigan, Med Ctr, Dept Internal Med, Div Pulm & Crit Care Med, Ann Arbor, MI 48109 USA
关键词
nonspecific interstitial pneumonia; pulmonary fibrosis;
D O I
10.1055/s-2006-957336
中图分类号
R4 [临床医学];
学科分类号
1002 [临床医学]; 100602 [中西医结合临床];
摘要
Nonspecific interstitial pneumonia (NSIP) describes a histopathologic pattern that can be seen in patients with immunodeficiency, drug or environmental exposures, and connective tissue diseases. The clinical diagnosis of NSIP, however, should be reserved for idiopathic cases in which no causative factor is identified. Patients typically present with cough, dyspnea, restrictive pulmonary physiology with decreased gas transfer, and ground-glass infiltrates on high-resolution computed tomography (HRCT). Response to immunosuppressive therapy is often successful; however, patients with progressive disease are at increased risk of subsequent mortality and should be considered for alternative treatment strategies such as lung transplantation.
引用
收藏
页码:652 / 658
页数:7
相关论文
共 79 条
[1]
Non-specific interstitial pneumonia: findings on sequential CT scans of nine patients [J].
Akira, M ;
Inoue, G ;
Yamamoto, S ;
Sakatani, M .
THORAX, 2000, 55 (10) :854-859
[2]
[Anonymous], 2002, AM J RESP CRIT CARE, V165, P277, DOI [DOI 10.1164/AJRCCM.165.2.ATS01, 10.1164/ajrccm.165.2.ats01]
[3]
Nonspecific interstitial pneumonia associated with polymyositis and dermatomyositis - Serial high-resolution CT findings and functional correlation [J].
Arakawa, H ;
Yamada, H ;
Kurihara, Y ;
Nakajima, Y ;
Takeda, A ;
Fukushima, Y ;
Fujioka, M .
CHEST, 2003, 123 (04) :1096-1103
[4]
HRCT diagnosis of diffuse parenchymal lung disease: interobserver variation [J].
Aziz, ZA ;
Wells, AU ;
Hansell, DM ;
Bain, GA ;
Copley, SJ ;
Desai, SR ;
Ellis, SM ;
Gleeson, FV ;
Grubnic, S ;
Nicholson, AG ;
Padley, SPG ;
Pointon, KS ;
Reynolds, JH ;
Robertson, RJH ;
Rubens, MB .
THORAX, 2004, 59 (06) :506-511
[5]
Prognostic significance of histopathologic subsets in idiopathic pulmonary fibrosis [J].
Bjoraker, JA ;
Ryu, JH ;
Edwin, MK ;
Myers, JL ;
Tazelaar, HD ;
Schroeder, DR ;
Offord, KP .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 157 (01) :199-203
[6]
ACUTE HYPOXEMIC RESPIRATORY-FAILURE IN CHILDREN FOLLOWING BONE-MARROW TRANSPLANTATION - AN OUTCOME AND PATHOLOGICAL-STUDY [J].
BOJKO, T ;
NOTTERMAN, DA ;
GREENWALD, BM ;
DEBRUIN, WJ ;
MAGID, MS ;
GODWIN, T .
CRITICAL CARE MEDICINE, 1995, 23 (04) :755-759
[7]
Histopathologic subsets of fibrosing alveolitis in patients with systemic sclerosis and their relationship to outcome [J].
Bouros, D ;
Wells, AU ;
Nicholson, AG ;
Colby, TV ;
Polychronopoulos, V ;
Pantelidis, P ;
Haslam, PL ;
Vassilakis, DA ;
Black, CM ;
du Bois, RM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 165 (12) :1581-1586
[8]
Interstitial lung disease in a baby with a de novo mutation in the SFTPC gene [J].
Brasch, F ;
Griese, M ;
Tredano, M ;
Johnen, G ;
Ochs, M ;
Rieger, C ;
Mulugeta, S ;
Müller, KM ;
Bahuau, M ;
Beers, MF .
EUROPEAN RESPIRATORY JOURNAL, 2004, 24 (01) :30-39
[9]
Nonspecific interstitial pneumonia and usual interstitial pneumonia with mutation in surfactant protein C in familial pulmonary fibrosis [J].
Chibbar, R ;
Shih, F ;
Baga, M ;
Torlakovic, E ;
Ramlall, K ;
Skomro, R ;
Cockcroft, DW ;
Lemire, EG .
MODERN PATHOLOGY, 2004, 17 (08) :973-980
[10]
Enhanced monocyte chemoattractant protein-3/CC chemokine ligand-7 in usual interstitial pneumonia [J].
Choi, ES ;
Lakubzick, C ;
Carpenter, KJ ;
Kunkel, SL ;
Evanoff, H ;
Martinez, FJ ;
Flaherty, KR ;
Toews, GB ;
Colby, TV ;
Kazerooni, EA ;
Gross, BH ;
Travis, WD ;
Hogaboam, CM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 170 (05) :508-515