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一例具有独特形态的小细胞肺癌合并病例:肿瘤发生机制的研究。

A case of combined small cell lung carcinoma with unique morphology: Investigation of tumorigenesis.

作者信息

Asahina Miki, Fukumura Yuki, Mamat Osman, Saito Tsuyoshi, Hayashi Takuo, Uekusa Toshimasa, Suzuki Kenji, Yao Takashi

机构信息

Department of Human Pathology, Juntendo University, School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo 113-8421, Japan.

Department of Diagnostic Pathology, Kanto Rosai Hospital, 1-1kizukisumiyoshi-cho, Nakahara-ku, Kawasaki City, Kanagawa 211-8510, Japan.

出版信息

Pathol Int. 2018 Nov;68(11):618-623. doi: 10.1111/pin.12726. Epub 2018 Oct 12.

Abstract

Small cell lung carcinoma (SCLC) usually grows in a pure form with no other associated histological components. However, combined small cell lung carcinoma (cSCLC), which is accompanied by other histological components (cSCLCs) may sometimes occur. Herein, we analyzed the tumorigenesis of cSCLC containing a demarcated area of pure SCLC. A 76-year-old man had a 25-mm mass in the perihilar portion of his right upper lung. Histologically, the cSCLC contained two relatively demarcated areas: one area composed of pure SCLC cells and another area of SCLC, squamous-like component (SLC), and spindle cell carcinoma (SpCC) cells. Loss of heterozygosity (LOH) was observed at allele 3p in all tumor components and at 22q in the pure SCLC component. Histological and immunohistochemical analysis and LOH study suggested that all components were likely to be monoclonal in origin and revealed that the pure SCLC component was not the precursor of the cSCLC. In the tumorigenesis of this case, the pure SCLC and the cSCLC may have originated from a common pluripotent tumor cell and then diverged, although we cannot state this conclusively. Further studies with more cases are necessary to test this theory.

摘要

小细胞肺癌(SCLC)通常以纯形式生长,不伴有其他相关组织学成分。然而,有时可能会出现伴有其他组织学成分的小细胞肺癌(cSCLC)。在此,我们分析了含有明确界定的纯SCLC区域的cSCLC的肿瘤发生情况。一名76岁男性右上肺门周围有一个25毫米的肿块。组织学上,cSCLC包含两个相对明确界定的区域:一个区域由纯SCLC细胞组成,另一个区域包含SCLC、鳞状样成分(SLC)和梭形细胞癌(SpCC)细胞。在所有肿瘤成分的3p等位基因以及纯SCLC成分的22q处均观察到杂合性缺失(LOH)。组织学和免疫组化分析以及LOH研究表明,所有成分可能起源于单克隆,并且显示纯SCLC成分不是cSCLC的前体。在该病例的肿瘤发生过程中,纯SCLC和cSCLC可能起源于一个共同的多能肿瘤细胞,然后发生分化,尽管我们不能确定地说明这一点。需要更多病例的进一步研究来验证这一理论。

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