Sugimoto Shinya, Yamada Hidetaka, Takahashi Masazumi, Morohoshi Yuichi, Yamaguchi Naotaka, Tsunoda Yuya, Hayashi Hiroyuki, Sugimura Haruhiko, Komatsu Hirokazu
Department of Gastroenterology, Yokohama Municipal Citizen's Hospital, 56 Okazawa-cho, Hodogaya-ku, Yokohama, Kanagawa, 240-8555, Japan.
Gastric Cancer. 2014 Oct;17(4):745-9. doi: 10.1007/s10120-013-0278-2. Epub 2013 Jun 29.
A 41-year-old man with no familial history of gastric cancer was diagnosed as with intramucosal early gastric cancer. Two months after the first endoscopic submucosal dissection for signet-ring cell carcinoma (SRCC), the appearance of previously unrecognized multiple erosions of SRCC was noticed. Pathological examination after a total gastrectomy and Roux-en-Y reconstruction with D2 lymph node dissection were performed. Postoperative pathological examination revealed 90 and more lesions, which tempted the attending pathologist to refer to genetic tests for the predisposition though the patient had no familial history of gastric cancer. There were no mutations in all the exons of CDH1 with conventional DNA sequencing, but multiplex ligation-dependent probe amplification, and reverse transcription-polymerase chain reaction analyses disclosed a large genomic deletion (c.1566-?_1711+?del), leading to the mRNA with loss of the exon 11. Among family members, his son was found to be a carrier of this change, while his parents were negative for the familial CDH1 mutation, implying that this change is a de novo event in the proband. The present report is the first description of a de novo large genomic deletion of CDH1 gene associated with early-onset diffuse gastric cancer. When the clinician finds a relatively-young patient who has multiple SRCCs, CDH1 germline mutation should be considered, even for patients with no familial history.
一名无胃癌家族史的41岁男性被诊断为黏膜内早期胃癌。在首次对印戒细胞癌(SRCC)进行内镜下黏膜下剥离术后两个月,发现了此前未被识别的多个SRCC糜烂灶。进行了全胃切除术及D2淋巴结清扫的Roux-en-Y重建术后的病理检查。术后病理检查发现90多个病灶,尽管该患者无胃癌家族史,但这促使主治病理学家考虑进行遗传易感性检测。常规DNA测序显示CDH1所有外显子均无突变,但多重连接依赖性探针扩增及逆转录-聚合酶链反应分析发现一个大的基因组缺失(c.1566-?_1711+?del),导致外显子11缺失的mRNA。在其家庭成员中,发现他的儿子是这种变化的携带者,而他的父母CDH1家族突变检测为阴性,这意味着这种变化在先证者中是一个新生事件。本报告首次描述了与早发性弥漫性胃癌相关的CDH1基因新生大基因组缺失。当临床医生发现一名患有多个SRCC的相对年轻患者时,即使其无家族史,也应考虑CDH1种系突变。