Histopathologic variability in usual and nonspecific interstitial pneumonias

被引:465
作者
Flaherty, KR
Travis, WD
Colby, TV
Toews, GB
Kazerooni, EA
Gross, BH
Jain, A
Strawderman, RL
Flint, A
Lynch, JP
Martinez, FJ
机构
[1] Univ Michigan Hlth Syst, Div Pulm & Crit Care Med, Ann Arbor, MI USA
[2] Univ Michigan Hlth Syst, Dept Radiol, Ann Arbor, MI USA
[3] Univ Michigan Hlth Syst, Dept Pathol, Ann Arbor, MI USA
[4] Univ Michigan, Sch Publ Hlth, Dept Biostat, Ann Arbor, MI 48109 USA
[5] Armed Forces Inst Pathol, Dept Pulm & Mediastinal Pathol, Washington, DC 20306 USA
[6] Mayo Clin, Dept Pathol, Scottsdale, AZ USA
关键词
pulmonary fibrosis; usual interstitial pneumonia; nonspecific interstitial pneumonia; idiopathic interstitial pneumonia; idiopathic pulmonary fibrosis;
D O I
10.1164/ajrccm.164.9.2103074
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Findings of surgical lung biopsy (SLB) are important in categorizing patients with idiopathic interstitial pneumonia (IIP). We investigated whether histologic variability would be evident in SLB specimens from multiple lobes in patients with IIP. SLBs from 168 patients, 109 of whom had. multiple lobes biopsied, were reviewed by three pathologists. A diagnosis was assigned to each lobe. A different diagnosis was found between lobes in 26% of the patients. Patients with usual interstitial pneumonia (UIP) in all lobes were categorized as concordant for UIP (n = 51) and those with UIP in at least one lobe were categorized as discordant for UIP (n = 28). Patients with nonspecific interstitial pneumonia (NSIP) in all, lobes were categorized as having fibrotic (n = 25) or cellular NSIP (n = 5). No consistent distribution of lobar histology was noted. Patients concordant for UIP were older (63 +/- 9 [mean +/- SD] yr; p < 0.05 as compared with all other groups) than those discordant for UIP (57 +/- 12 yr) or with fibrotic NSIP (56 +/- 11 yr) or cellular NSIP (50 +/- 9 yr). Semiquantitative high-resolution computed tomography demonstrated a varied profusion of fibrosis (p < 0.05 for all group comparisons), with more fibrosis in concordant UIP (2.13 <plus/minus> 0.62) than in discordant UIP (1.42 +/- 0.73), fibrotic NSIP (0.83 +/- 0.58), or cellular NSIP (0.44 +/- 0.42). Survival was better for patients with NSIP than for those in both UIP groups (p < 0.001), although survival in the two UIP groups was comparable (p = 0.16). Lobar histologic variability is frequent in patients with IIP, patients with a histologic pattern of UIP in any lobe should be classified as having UIP.
引用
收藏
页码:1722 / 1727
页数:6
相关论文
共 24 条
[1]  
[Anonymous], 2000, AM J RESP CRIT CARE, V161, P646, DOI DOI 10.1164/AJRCCM.161.2.ATS3-00
[2]   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
[3]   QUANTITATIVE ASSESSMENT OF LUNG PATHOLOGY IN IDIOPATHIC PULMONARY FIBROSIS [J].
CHERNIACK, RM ;
COLBY, TV ;
FLINT, A ;
THURLBECK, WM ;
WALDRON, J ;
ACKERSON, L ;
KING, TE .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1991, 144 (04) :892-900
[4]   A histologic pattern of nonspecific interstitial pneumonia is associated with a better prognosis than usual interstitial pneumonia in patients with cryptogenic fibrosing alveolitis [J].
Daniil, ZD ;
Gilchrist, FC ;
Nicholson, AG ;
Hansell, DM ;
Harris, J ;
Colby, TV ;
du Bois, RM .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 160 (03) :899-905
[5]   Steroids in idiopathic pulmonary fibrosis: A prospective assessment of adverse reactions, response to therapy, and survival [J].
Flaherty, KR ;
Toews, GB ;
Lynch, JP ;
Kazerooni, EA ;
Gross, BH ;
Strawderman, RL ;
Hariharan, K ;
Flint, A ;
Martinez, FJ .
AMERICAN JOURNAL OF MEDICINE, 2001, 110 (04) :278-282
[6]   Influence of sample number and biopsy site on the histologic diagnosis of diffuse lung disease [J].
Flint, A ;
Martinez, FJ ;
Young, ML ;
Whyte, RI ;
Toews, GB ;
Lynch, JP .
ANNALS OF THORACIC SURGERY, 1995, 60 (06) :1605-1607
[7]   Clinical features of three fatal cases of non-specific interstitial pneumonia [J].
Fujita, J ;
Yamadori, I ;
Bandoh, S ;
Mizobuchi, K ;
Suemitsu, I .
INTERNAL MEDICINE, 2000, 39 (05) :407-411
[8]   Idiopathic pulmonary fibrosis - Predicting response to therapy and survival [J].
Gay, SE ;
Kazerooni, EA ;
Toews, CB ;
Lynch, JP ;
Gross, BH ;
Cascade, PN ;
Spizarny, DL ;
Flint, A ;
Schork, MA ;
Whyte, RI ;
Popovich, J ;
Hyzy, R ;
Martinez, FJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1998, 157 (04) :1063-1072
[9]   High-resolution computed tomography in the evaluation of fibrosing alveolitis [J].
Hansell, DM .
CLINICS IN CHEST MEDICINE, 1999, 20 (04) :739-+
[10]   Nonspecific interstitial pneumonia:: Variable appearance at high-resolution chest CT [J].
Hartman, TE ;
Swensen, SJ ;
Hansell, DM ;
Colby, TV ;
Myers, JL ;
Tazelaar, HD ;
Nicholson, AG ;
Wells, AU ;
Rau, JH ;
Mu'adhdhin, DE ;
du Bois, RM ;
Müller, NL .
RADIOLOGY, 2000, 217 (03) :701-705