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Clinical, radiological, and pathological evaluation of “NSIP with OP overlap” pattern compared with NSIP in patients with idiopathic interstitial pneumonias - 18/11/20

Doi : 10.1016/j.rmed.2020.106201 
Noriyuki Enomoto a, b, , Hiromitsu Sumikawa c, Hiroaki Sugiura d, Masashi Kitani e, Tomonori Tanaka f, Hironao Hozumi a, Tomoyuki Fujisawa a, Takafumi Suda a
a Second Division, Department of Internal Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan 
b Health Administration Center, Hamamatsu University School of Medicine, Hamamatsu, Japan 
c Department of Diagnostic Radiology, Sakai City Medical Centre, Osaka, Japan 
d Department of Radiology, National Defense Medical College, Saitama, Japan 
e Department of Pathology, National Hospital Organization Tokyo National Hospital, Tokyo, Japan 
f Department of Diagnostic Pathology, Kobe University Hospital, Hyogo, Japan 

Corresponding author. Health Administration Center Hamamatsu University School of Medicine, 1-20-1 Handayama, Hamamatsu, 431-3192, Japan.Health Administration Center Hamamatsu University School of Medicine1-20-1 HandayamaHamamatsu431-3192Japan

Abstract

Background

Nonspecific interstitial pneumonia (NSIP) and organizing pneumonia (OP) are major subtypes of idiopathic interstitial pneumonias (IIPs) and closely related to connective tissue diseases (CTDs). “NSIP with OP overlap” is a controversial finding that has recently appeared in the criteria of interstitial pneumonia with autoimmune features (IPAF). However, details of this controversial entity are not well known.

Objective

To determine the frequency of “NSIP with OP overlap” pattern in IIPs and to identify differences from idiopathic NSIP (iNSIP).

Methods

In 524 patients with interstitial pneumonia from 39 institutes who underwent surgical lung biopsy, 444 were diagnosed as IIPs by a multidisciplinary discussion meeting via a cloud-based integrated database. Among these patients, 44 (9.9%) who had iNSIP and 21 (4.7%) with histopathologically-defined “NSIP with OP overlap” pattern (a pathological NSIP and OP pattern, but without a UIP pattern) were retrospectively studied.

Results

Patients with “NSIP with OP overlap” pattern showed a significantly greater extent of consolidation (p < 0.001), more subpleural ground glass attenuation (p = 0.036), and more peripheral + bronchovascular distribution (p = 0.009) on high-resolution computed tomography than those with iNSIP. The incidences of newly-developed CTDs during follow-up was similar between the groups and polymyositis/dermatomyositis was the most frequent CTD in both groups. Nearly half of the patients fulfilled IPAF criteria, but no significant difference was found between iNSIP and “NSIP with OP overlap” pattern (47.7% vs. 42.9, p = 0.712). The incidence of acute exacerbation and the survival rates were similar between the groups.

Conclusions

The incidence of “NSIP with OP overlap” pattern is 4.7% in IIPs. The frequency of newly-developed CTDs during follow-up, mainly polymyositis/dermatomyositis, the frequency of acute exacerbation, and the survival rate in “NSIP with OP overlap” pattern are similar to those of iNSIP.

Il testo completo di questo articolo è disponibile in PDF.

Highlights

A controversial disease entity of “NSIP with OP overlap” pattern attracts attention in IPAF criteria.
In 444 patients with IIPs, 21 (4.7%) were classified as histopathologically-defined “NSIP with OP overlap” pattern.
The frequency of CTDs, mainly PM/DM, and that of acute exacerbation in “NSIP with OP overlap” pattern were similar to those of idiopathic NSIP.
Prognosis in patients with “NSIP with OP overlap” pattern was favorable and also similar to that of idiopathic NSIP.

Il testo completo di questo articolo è disponibile in PDF.

Keywords : Idiopathic interstitial pneumonia, Interstitial pneumonia with autoimmune features, Nonspecific interstitial pneumonia, Organizing pneumonia, Unclassifiable interstitial pneumonia


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