Morphological, immunohistochemical, and genetic analyses of bronchiolar adenoma and its putative variants

Abstract We collected 26 cases of bronchiolar adenoma (BA) and its variants, and performed a comprehensive characterization using a combination of morphological, immunohistochemical, and genetic assessments. Of these 26, 13 were classic bilayered cases, including 10 proximal and 3 distal‐type BAs. O...

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Main Authors: Jinchen Shao, Jiani C Yin, Hairong Bao, Ruiying Zhao, Yuchen Han, Lei Zhu, Xue Wu, Yang Shao, Jie Zhang
Format: Article
Language:English
Published: Wiley 2021-05-01
Series:The Journal of Pathology: Clinical Research
Subjects:
Online Access:https://doi.org/10.1002/cjp2.197
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spelling doaj-6c3b286dabfe44989f37db4b16a0f7f62021-04-26T10:28:15ZengWileyThe Journal of Pathology: Clinical Research2056-45382021-05-017328730010.1002/cjp2.197Morphological, immunohistochemical, and genetic analyses of bronchiolar adenoma and its putative variantsJinchen Shao0Jiani C Yin1Hairong Bao2Ruiying Zhao3Yuchen Han4Lei Zhu5Xue Wu6Yang Shao7Jie Zhang8Department of Pathology, Shanghai Chest Hospital Shanghai Jiao Tong University Shanghai PR ChinaNanjing Geneseeq Technology Inc. Nanjing PR ChinaNanjing Geneseeq Technology Inc. Nanjing PR ChinaDepartment of Pathology, Shanghai Chest Hospital Shanghai Jiao Tong University Shanghai PR ChinaDepartment of Pathology, Shanghai Chest Hospital Shanghai Jiao Tong University Shanghai PR ChinaDepartment of Pathology, Shanghai Chest Hospital Shanghai Jiao Tong University Shanghai PR ChinaNanjing Geneseeq Technology Inc. Nanjing PR ChinaNanjing Geneseeq Technology Inc. Nanjing PR ChinaDepartment of Pathology, Shanghai Chest Hospital Shanghai Jiao Tong University Shanghai PR ChinaAbstract We collected 26 cases of bronchiolar adenoma (BA) and its variants, and performed a comprehensive characterization using a combination of morphological, immunohistochemical, and genetic assessments. Of these 26, 13 were classic bilayered cases, including 10 proximal and 3 distal‐type BAs. Of note, we also identified 13 cases that lacked a continuous basal cell layer. In five cases, the adenomas were partially classic bilayered, leaving a single layer of columnar or cuboidal epithelial cells in some areas of the lesion (BA with monolayered cell lesions). In the other eight cases, the glandular or papillary structures were entirely composed of monolayered columnar or cuboidal epithelial cells, which were morphologically identical to the luminal epithelial cells of classic BA (monolayered BA‐like lesions). Immunohistochemical analysis revealed thyroid transcription factor 1 expression by ciliated columnar epithelial cells, basal cells, and nonciliated columnar and cuboidal epithelial cells. Basal cells also expressed p40 and p63. Twenty‐five cases underwent next‐generation sequencing using a 422‐cancer‐gene panel (GeneseeqPrime). Oncogenic driver mutations were detected in 23 cases, including 13 (52%) with EGFR mutations, 4 (16%) with KRAS G12D/V mutations, 3 (12%) with BRAF V600E mutations, 2 (8%) with ERBB2 exon 20 insertions, and 1 (4%) with a RET fusion. EGFR exon 20 insertions were present in 100% of BAs with monolayered cell lesions, 37.5% of monolayered BA‐like lesions, and 8% of classic BA (Fisher's exact test, p = 0.002, false discovery rate = 0.014). Collectively, our study revealed a gradual morphological transition between BA and its variants. The genetic composition of BAs with monolayered structures differed significantly from those of classic BAs or lung adenocarcinoma.https://doi.org/10.1002/cjp2.197bronchiolar adenomamonolayered lesionsnext‐generation sequencingEGFR exon 20 insertions
collection DOAJ
language English
format Article
sources DOAJ
author Jinchen Shao
Jiani C Yin
Hairong Bao
Ruiying Zhao
Yuchen Han
Lei Zhu
Xue Wu
Yang Shao
Jie Zhang
spellingShingle Jinchen Shao
Jiani C Yin
Hairong Bao
Ruiying Zhao
Yuchen Han
Lei Zhu
Xue Wu
Yang Shao
Jie Zhang
Morphological, immunohistochemical, and genetic analyses of bronchiolar adenoma and its putative variants
The Journal of Pathology: Clinical Research
bronchiolar adenoma
monolayered lesions
next‐generation sequencing
EGFR exon 20 insertions
author_facet Jinchen Shao
Jiani C Yin
Hairong Bao
Ruiying Zhao
Yuchen Han
Lei Zhu
Xue Wu
Yang Shao
Jie Zhang
author_sort Jinchen Shao
title Morphological, immunohistochemical, and genetic analyses of bronchiolar adenoma and its putative variants
title_short Morphological, immunohistochemical, and genetic analyses of bronchiolar adenoma and its putative variants
title_full Morphological, immunohistochemical, and genetic analyses of bronchiolar adenoma and its putative variants
title_fullStr Morphological, immunohistochemical, and genetic analyses of bronchiolar adenoma and its putative variants
title_full_unstemmed Morphological, immunohistochemical, and genetic analyses of bronchiolar adenoma and its putative variants
title_sort morphological, immunohistochemical, and genetic analyses of bronchiolar adenoma and its putative variants
publisher Wiley
series The Journal of Pathology: Clinical Research
issn 2056-4538
publishDate 2021-05-01
description Abstract We collected 26 cases of bronchiolar adenoma (BA) and its variants, and performed a comprehensive characterization using a combination of morphological, immunohistochemical, and genetic assessments. Of these 26, 13 were classic bilayered cases, including 10 proximal and 3 distal‐type BAs. Of note, we also identified 13 cases that lacked a continuous basal cell layer. In five cases, the adenomas were partially classic bilayered, leaving a single layer of columnar or cuboidal epithelial cells in some areas of the lesion (BA with monolayered cell lesions). In the other eight cases, the glandular or papillary structures were entirely composed of monolayered columnar or cuboidal epithelial cells, which were morphologically identical to the luminal epithelial cells of classic BA (monolayered BA‐like lesions). Immunohistochemical analysis revealed thyroid transcription factor 1 expression by ciliated columnar epithelial cells, basal cells, and nonciliated columnar and cuboidal epithelial cells. Basal cells also expressed p40 and p63. Twenty‐five cases underwent next‐generation sequencing using a 422‐cancer‐gene panel (GeneseeqPrime). Oncogenic driver mutations were detected in 23 cases, including 13 (52%) with EGFR mutations, 4 (16%) with KRAS G12D/V mutations, 3 (12%) with BRAF V600E mutations, 2 (8%) with ERBB2 exon 20 insertions, and 1 (4%) with a RET fusion. EGFR exon 20 insertions were present in 100% of BAs with monolayered cell lesions, 37.5% of monolayered BA‐like lesions, and 8% of classic BA (Fisher's exact test, p = 0.002, false discovery rate = 0.014). Collectively, our study revealed a gradual morphological transition between BA and its variants. The genetic composition of BAs with monolayered structures differed significantly from those of classic BAs or lung adenocarcinoma.
topic bronchiolar adenoma
monolayered lesions
next‐generation sequencing
EGFR exon 20 insertions
url https://doi.org/10.1002/cjp2.197
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