Literature DB >> 23364926

High-resolution CT scan findings in familial interstitial pneumonia do not conform to those of idiopathic interstitial pneumonia.

Ho Yun Lee1, Joon Beom Seo1, Mark P Steele2, Marvin I Schwarz3, Kevin K Brown3, James E Loyd4, Janet L Talbert3, David A Schwartz3, David A Lynch5.   

Abstract

BACKGROUND: The aim of this study was to describe the high-resolution CT (HRCT) scan features that characterize familial interstitial pneumonia (FIP).
METHODS: FIP was defined by the presence of two or more cases of probable or definite idiopathic interstitial pneumonia (IIP) in individuals related within three degrees. The cases were collected consecutively from three centers. We identified 371 individuals with potential FIP from 289 families, including 340 individuals who had HRCT scans. Two chest radiologists independently reviewed the HRCT scans, scoring the extent and distribution of HRCT scan findings, and assessed the overall radiologic diagnosis.
RESULTS: HRCT scan abnormalities suggestive of IIP were present in 85% (289 of 340 subjects). The most frequent findings were reticular pattern (n = 238, 82%) and ground-glass opacity (GGO) associated with reticular abnormality (n = 231, 80%). Other changes included GGO in 116 (40%), honeycombing in 92 (32%), and micronodules in 65 (22%). In the 289 cases with evidence of IIP, the findings were diffusely distributed in the craniocaudal plane in 186 (64%), and the lower lung zones were predominantly involved in 89 (31%). In the axial plane, 194 (67%) had a subpleural distribution; 88 (30%) were diffuse. The imaging pattern was classified as definite or probable usual interstitial pneumonia (UIP) in only 62 subjects (22%) and definite or probable nonspecific interstitial pneumonia (NSIP) in 35 subjects (12%). In 160 subjects (55%), the imaging findings did not conform to previously described UIP or NSIP patterns.
CONCLUSIONS: Reticulation and a mixed GGO/reticular pattern are the most common HRCT scan findings in FIP. The parenchymal abnormalities are most often diffuse in the craniocaudal dimension and have a predominantly peripheral distribution in the axial dimension. Although a radiologic UIP pattern is not uncommon, most cases do not conform to typical UIP or NSIP patterns.

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Mesh:

Year:  2012        PMID: 23364926      PMCID: PMC3515030          DOI: 10.1378/chest.11-2812

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  25 in total

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2.  Clinical and pathologic features of familial interstitial pneumonia.

Authors:  Mark P Steele; Marcy C Speer; James E Loyd; Kevin K Brown; Aretha Herron; Susan H Slifer; Lauranell H Burch; Momen M Wahidi; John A Phillips; Thomas A Sporn; H Page McAdams; Marvin I Schwarz; David A Schwartz
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3.  Fleischner Society: glossary of terms for thoracic imaging.

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5.  Gene expression profiling of familial and sporadic interstitial pneumonia.

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Review 6.  Idiopathic pulmonary fibrosis: is it a familial disease?

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Authors:  Carolina Althoff Souza; Nestor L Müller; Kyung Soo Lee; Takeshi Johkoh; Hiromitsu Mitsuhiro; Semin Chong
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Authors:  Rachel K Putman; Gunnar Gudmundsson; Gisli Thor Axelsson; Tomoyuki Hida; Osamu Honda; Tetsuro Araki; Masahiro Yanagawa; Mizuki Nishino; Ezra R Miller; Gudny Eiriksdottir; Elías F Gudmundsson; Noriyuki Tomiyama; Hiroshi Honda; Ivan O Rosas; George R Washko; Michael H Cho; David A Schwartz; Vilmundur Gudnason; Hiroto Hatabu; Gary M Hunninghake
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Authors:  Jonathan A Kropski; Jason M Pritchett; Donald F Zoz; Peter F Crossno; Cheryl Markin; Errine T Garnett; Amber L Degryse; Daphne B Mitchell; Vasiliy V Polosukhin; Otis B Rickman; Leena Choi; Dong-Sheng Cheng; Melinda E McConaha; Brittany R Jones; Linda A Gleaves; Frank B McMahon; John A Worrell; Joseph F Solus; Lorraine B Ware; Jae Woo Lee; Pierre P Massion; Rinat Zaynagetdinov; Eric S White; Jonathan D Kurtis; Joyce E Johnson; Steve D Groshong; Lisa H Lancaster; Lisa R Young; Mark P Steele; John A Phillips Iii; Joy D Cogan; James E Loyd; William E Lawson; Timothy S Blackwell
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5.  Accumulation of periostin in acute exacerbation of familial idiopathic pulmonary fibrosis.

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7.  MUC5B promoter polymorphism and interstitial lung abnormalities.

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8.  CT Imaging Phenotypes of Pulmonary Fibrosis in the MUC5B Promoter Site Polymorphism.

Authors:  Jonathan H Chung; Anna L Peljto; Ashish Chawla; Janet L Talbert; David F McKean; Byung-Hak Rho; Tasha E Fingerlin; Marvin I Schwarz; David A Schwartz; David A Lynch
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9.  Development and Progression of Interstitial Lung Abnormalities in the Framingham Heart Study.

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Review 10.  Familial Pulmonary Fibrosis: Genetic Features and Clinical Implications.

Authors:  David Zhang; Chad A Newton
Journal:  Chest       Date:  2021-06-26       Impact factor: 9.410

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