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Classification of Centrilobular Emphysema Based on CT-Pathologic Correlations

INTRODUCTION: Centrilobular emphysema (CLE) is recognized as low attenuation areas (LAA) with centrilobular distribution on high-resolution computed tomography. The LAA often exhibit a variety of shape or sharpness of border. This study was performed to elucidate the relationship between morphologic...

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Autores principales: Takahashi, Mamoru, Yamada, Gen, Koba, Hiroyuki, Takahashi, Hiroki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527991/
https://www.ncbi.nlm.nih.gov/pubmed/23264837
http://dx.doi.org/10.2174/1874306401206010155
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author Takahashi, Mamoru
Yamada, Gen
Koba, Hiroyuki
Takahashi, Hiroki
author_facet Takahashi, Mamoru
Yamada, Gen
Koba, Hiroyuki
Takahashi, Hiroki
author_sort Takahashi, Mamoru
collection PubMed
description INTRODUCTION: Centrilobular emphysema (CLE) is recognized as low attenuation areas (LAA) with centrilobular distribution on high-resolution computed tomography. The LAA often exhibit a variety of shape or sharpness of border. This study was performed to elucidate the relationship between morphological features of LAA and pathological findings in CLE. MATERIALS AND METHODS: The inflated-fixed lungs from 50 patients with CLE (42 males, 8 females; 14 operated, 36 autopsied) were examined by a method of CT-pathologic correlations that consisted of three steps. The first, CT images of the sliced lungs of the inflated-fixed lung specimens were examined on the shape and the peripheral border of each LAA. The second, the sliced lungs were radiographed in contact with high magnification. The third, the surface of the sliced lungs was observed by using stereomicroscopy. The views at low magnification of stereomicroscope were compared with the radiographs and the CT images of the same sample. RESULTS: Using CT-pathologic correlations, LAAs of CLE were classified into three types as follows; round or oval shape with well-defined border (Type A), polygonal or irregular shape with ill-defined border and less than 5 mm in diameter (Type B), and irregular shape with ill-defined border and 5 mm or over in diameter (Type C). Type A, Type B and Type C LAA were mainly related to dilatation of bronchioles, destruction of proximal part of alveolar ducts, and destruction of distal part of alveolar ducts, respectively. Type A, Type B and Type C were dominant LAA in 5 (10%), 29 (58%) and 12 (24%) patients, respectively. However, remained 4 patients (8%) did not show dominant LAA type. CONCLUSION: Morphological features of LAA in CLE may depend on dilatation or destruction of certain parts of the secondary lobule. Type B LAA was the commonest type in CLE.
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spelling pubmed-35279912012-12-21 Classification of Centrilobular Emphysema Based on CT-Pathologic Correlations Takahashi, Mamoru Yamada, Gen Koba, Hiroyuki Takahashi, Hiroki Open Respir Med J Article INTRODUCTION: Centrilobular emphysema (CLE) is recognized as low attenuation areas (LAA) with centrilobular distribution on high-resolution computed tomography. The LAA often exhibit a variety of shape or sharpness of border. This study was performed to elucidate the relationship between morphological features of LAA and pathological findings in CLE. MATERIALS AND METHODS: The inflated-fixed lungs from 50 patients with CLE (42 males, 8 females; 14 operated, 36 autopsied) were examined by a method of CT-pathologic correlations that consisted of three steps. The first, CT images of the sliced lungs of the inflated-fixed lung specimens were examined on the shape and the peripheral border of each LAA. The second, the sliced lungs were radiographed in contact with high magnification. The third, the surface of the sliced lungs was observed by using stereomicroscopy. The views at low magnification of stereomicroscope were compared with the radiographs and the CT images of the same sample. RESULTS: Using CT-pathologic correlations, LAAs of CLE were classified into three types as follows; round or oval shape with well-defined border (Type A), polygonal or irregular shape with ill-defined border and less than 5 mm in diameter (Type B), and irregular shape with ill-defined border and 5 mm or over in diameter (Type C). Type A, Type B and Type C LAA were mainly related to dilatation of bronchioles, destruction of proximal part of alveolar ducts, and destruction of distal part of alveolar ducts, respectively. Type A, Type B and Type C were dominant LAA in 5 (10%), 29 (58%) and 12 (24%) patients, respectively. However, remained 4 patients (8%) did not show dominant LAA type. CONCLUSION: Morphological features of LAA in CLE may depend on dilatation or destruction of certain parts of the secondary lobule. Type B LAA was the commonest type in CLE. Bentham Open 2012-12-14 /pmc/articles/PMC3527991/ /pubmed/23264837 http://dx.doi.org/10.2174/1874306401206010155 Text en © Takahashi et al.; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Takahashi, Mamoru
Yamada, Gen
Koba, Hiroyuki
Takahashi, Hiroki
Classification of Centrilobular Emphysema Based on CT-Pathologic Correlations
title Classification of Centrilobular Emphysema Based on CT-Pathologic Correlations
title_full Classification of Centrilobular Emphysema Based on CT-Pathologic Correlations
title_fullStr Classification of Centrilobular Emphysema Based on CT-Pathologic Correlations
title_full_unstemmed Classification of Centrilobular Emphysema Based on CT-Pathologic Correlations
title_short Classification of Centrilobular Emphysema Based on CT-Pathologic Correlations
title_sort classification of centrilobular emphysema based on ct-pathologic correlations
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3527991/
https://www.ncbi.nlm.nih.gov/pubmed/23264837
http://dx.doi.org/10.2174/1874306401206010155
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