Scinovex
articleTop 1% cited

Idiopathic Nonspecific Interstitial Pneumonia: Prognostic Significance of Cellular and Fibrosing Patterns

The American Journal of Surgical Pathology · 2000 · Vol. 24(1) · pp. 19–19
William D. TravisKazuhiro MatsuiJoel MossVictor J. Ferrans

Abstract

Nonspecific interstitial pneumonia (NSIP) has been proposed as a histologic subtype of idiopathic interstitial pneumonia with lung biopsy findings that are inconsistent with those of other idiopathic interstitial pneumonias. NSIP has a broad spectrum of histologic findings and a variable prognosis. The aim of this study was to determine whether it would be preferable to subdivide NSIP into cellular and fibrosing patterns. The authors classified lung biopsies from 101 patients with idiopathic interstitial lung disease as having histologic patterns of desquamative interstitial pneumonia (DIP), usual interstitial pneumonia (UIP), or cellular or fibrosing NSIP. Survival analysis was performed using the Kaplan-Meier method. Due to histologic, clinical, and survival similarities, the patients with idiopathic NSIP with lung biopsies that showed fibrosing as well as fibrosing and cellular patterns were combined into a single group of NSIP, fibrosing pattern. Of the 101 patients, 16 patients (9 women, 7 men) had idiopathic DIP; 56 patients (17 women, 39 men) had idiopathic UIP; 22 patients (7 women, 15 men) had idiopathic NSIP, fibrosing pattern; and 7 patients (2 women, 5 men) had idiopathic NSIP, cellular pattern. The patients had a mean age of 42, 51, 50, and 39 years respectively. Patients with idiopathic NSIP, cellular pattern had a better 5- and 10-year survival than those with idiopathic NSIP, fibrosing pattern (100% vs 90% and 100% vs 35% respectively, p = 0.027). Survival of patients with idiopathic UIP was worse than that of patients with idiopathic NSIP, fibrosing pattern (p = 0.014). The difference, however, was more evident at 5 years (43% vs 90%) than at 10 years (15% vs 35%). The 5- and 10-year survival of patients with idiopathic NSIP, cellular pattern and DIP was 100%, which was significantly better than that of patients with idiopathic UIP (p <0.0001). Based on these data, NSIP should be separated into cellular and fibrosing patterns, because these histologic patterns are associated with different clinical characteristics and prognoses.

Interstitial Lung Diseases and Idiopathic Pulmonary FibrosisOccupational and environmental lung diseasesInhalation and Respiratory Drug DeliveryMedicineIdiopathic interstitial pneumoniaUsual interstitial pneumoniaIdiopathic pulmonary fibrosisPathologyInterstitial lung diseaseLung biopsyLungBiopsyInternal medicine

MeSH terms

AdultAge FactorsAgedBiopsyDiagnosis, DifferentialFemaleHumansLungMaleMiddle AgedPulmonary FibrosisRisk FactorsSmokingTime FactorsSurvival Analysis
Citations
528
FWCI
28.39
field-weighted impact
References
24
Percentile
100%
vs. same field & year
Citations per year
References
Idiopathic Pulmonary Fibrosis: Clinical Relevance of Pathologic Classification
American Journal of Respiratory and Critical Care Medicine · 1998 · 1,258 citations
Nonspecific Interstitial Pneumonia/Fibrosis
The American Journal of Surgical Pathology · 1994 · 756 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.