A clinicopathologic and molecular analysis of five cases of bronchiolar adenoma with rare mutations.

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作者： Naoko,Takeda-Miyata ^[1] ; Aya,Miyagawa-Hayashino ^[1] ; Shinshichi,Hamada ^[2] ; Michiko,Nagamine ^[1] ; Tomomi,Fujii ^[3] ; Tetsuya,Imura ^[1] ; Hiroaki,Tsunezuka ^[4] ; Masanori,Shimomura ^[4] ; Tadanori,Yamaguchi ^[5] ; Masashi,Yanada ^[6] ; Masayoshi,Inoue ^[4] ; Eiichi,Konishi ^[1]

作者单位： Department of Surgical Pathology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan. ^[1] Department of Pathology, Otsu City Hospital, Shiga, Japan. ^[2] Department of Diagnostic Pathology, Nara Medical University School of Medicine, Nara, Japan. ^[3] Department of Surgery, Division of Thoracic Surgery, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan. ^[4] Department of Clinical Laboratory, Ayabe City Hospital, Kyoto, Japan. ^[5] Department of Thoracic Surgery, Otsu City Hospital, Shiga, Japan. ^[6]

关键词 ALK rearrangement BRAF V600E NRAS bronchiolar adenoma ciliated muconodular papillary tumor

主题词腺瘤(Adenoma);人类(Humans);肺肿瘤(Lung Neoplasms);突变(Mutation);原癌基因蛋白质B-raf(Proto-Oncogene Proteins B-raf);原癌基因蛋白质类p21(ras)(Proto-Oncogene Proteins p21(ras));受体蛋白质酪氨酸激酶类(Receptor Protein-Tyrosine Kinases)

DOI 10.1111/pin.13213

PMID 35234319

发布时间 2022-05-18

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