Evidence map›Paper›PMID 36988010›Full record

ArticleHistology and histopathology2023

Clinicopathological features and genomic analysis of bronchiolar adenoma.

Jiaqi Bo, Xue Chen, Tingting Zhang, Xuyou Zhu, Long Zhang, Yuting Liu, Haoyang Zhang, Caixia Wu, Shunyan Mou, Xianghua Yi and 2 more

Abstract read
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In one paragraph

Article in Histology and histopathology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 26% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 3 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 1 country.

Jiaqi BoDepartment of Pathology, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Xue Chen *Department of Pathology, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Tingting Zhang *Department of Pathology, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Xuyou Zhu *Department of Pathology, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Long ZhangDepartment of Pathology, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Yuting LiuDepartment of Pathology, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Haoyang ZhangDepartment of Pathology, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Caixia WuDepartment of Pathology, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Shunyan MouDepartment of Pathology, Tongji Hospital, Tongji University School of Medicine, Shanghai, China.
Xianghua YiDepartment of Pathology, Tongji Hospital, Tongji University School of Medicine, Shanghai, China. yixhxf@163.com.
Weiwei RuiDepartment of Pathology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. rww11847@rjh.com.cn.
Yu ZengDepartment of Pathology, Tongji Hospital, Tongji University School of Medicine, Shanghai, China. yuzeng2013@163.com.
Tongji University · CNTongji Hospital · CN

Funding

Clinical Research Project of Tongji Hospital of Tongji University ITJ(QN) 1907National Natural Science Foundation of China 81401882National Natural Science Foundation of China 82170082Research Project of Shanghai Putuo District Eastern integrated health care system YLT2103Shanghai Municipal Science and Technology Commission 2021 Medical Innovation Research Project 21Y11908800
6 · The paper itself

Abstract

backgroundBronchiolar adenoma (BA) is a rare tumor of the bronchioles with a double-layer structure, including the basal cell layer and the superficial cell layer, and it has a good prognosis. However, the concept of a putative variant of BA has been proposed in the recent literature.

methodsData on 17 cases of BA were collected from our center. The clinical data, morphology, immunophenotype, and molecular changes were retrospectively analyzed. We also collected the molecular changes in BA reported in the previous literature and summarized the putative driver mutations of BA.

resultsOut of 17 BAs, 13 were classic cases with a double-layer structure, including 9 proximal-type and 4 distal-type BAs. Of note, we also identified 3 cases that lacked a continuous basal cell layer, including 2 cases of mixed-type BA with monolayered lesions (basal cells were undetected in some areas) and 1 case of a monolayered BA-like lesion (basal cells were completely undetected). The immunohistochemical findings of monolayer cell lesions were closer to those of minimally invasive adenocarcinoma. We also found one case in which BA transformed into invasive adenocarcinoma accompanied by mutations in the TP53, JAK2, NF1 and RB1 genes. Combined with the previous literature, the most common putative driver gene mutations in 62 BA lesions were EGFR (25/62; 41%) and BRAF (21/62; 34.4%).

conclusionTypical BA has a double-layer cell structure; however, there is also a putative variant of BA, which has a monolayer cell structure and lacks the basal cell layer. Transformation from BA into invasive adenocarcinoma is unusual but can occur.

Indexed as

AdenocarcinomaAdenomaLung NeoplasmsBronchiolesGenomicsHumansMutationRetrospective Studies

Identifiers

PMID36988010
OpenAlexW4361305473

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.