Succinate dehydrogenase B-deficient renal cell carcinoma with a germline variant in a Japanese patient: a case report.

IF 1 Q4 GENETICS & HEREDITY Human Genome Variation Pub Date : 2022-07-22 DOI:10.1038/s41439-022-00202-z
Shinichiro Higashi, Takeshi Sasaki, Katsunori Uchida, Takumi Kageyama, Makoto Ikejiri, Ryuki Matsumoto, Manabu Kato, Satoru Masui, Yuko Yoshio, Kouhei Nishikawa, Yoshinaga Okugawa, Masatoshi Watanabe, Takahiro Inoue
{"title":"Succinate dehydrogenase B-deficient renal cell carcinoma with a germline variant in a Japanese patient: a case report.","authors":"Shinichiro Higashi,&nbsp;Takeshi Sasaki,&nbsp;Katsunori Uchida,&nbsp;Takumi Kageyama,&nbsp;Makoto Ikejiri,&nbsp;Ryuki Matsumoto,&nbsp;Manabu Kato,&nbsp;Satoru Masui,&nbsp;Yuko Yoshio,&nbsp;Kouhei Nishikawa,&nbsp;Yoshinaga Okugawa,&nbsp;Masatoshi Watanabe,&nbsp;Takahiro Inoue","doi":"10.1038/s41439-022-00202-z","DOIUrl":null,"url":null,"abstract":"<p><p>Succinate dehydrogenase (SDH)-deficient renal cell carcinoma (RCC) is a rare renal cancer. A 75-year-old Japanese female presented with gross hematuria. Computed tomography revealed two tumors in the left kidney, which were resected. Immunohistochemistry indicated negative staining for the B subunit of SDH (SDHB) in the resected specimen, leading to a final diagnosis of SDHB-deficient RCC. Genetic testing for SDHB showed a RCC germline variant in exon 6 (NM_003000.3:c.642 G > C) that was previously reported but associated with a novel phenotype (i.e., RCC). Twenty-six years prior, her daughter, who was 25 years old at the time, had undergone radical nephrectomy for a pathologic diagnosis of renal oncocytoma of the right kidney; SDHB immunostaining of her daughter's tumor was also negative retrospectively. We confirmed that her daughter carried the germline variant in SDHB exon 6, similar to the patient. The patient had no evidence of disease progression at 15 months after surgery.</p>","PeriodicalId":36861,"journal":{"name":"Human Genome Variation","volume":"9 1","pages":"25"},"PeriodicalIF":1.0000,"publicationDate":"2022-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9307839/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Genome Variation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1038/s41439-022-00202-z","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

Succinate dehydrogenase (SDH)-deficient renal cell carcinoma (RCC) is a rare renal cancer. A 75-year-old Japanese female presented with gross hematuria. Computed tomography revealed two tumors in the left kidney, which were resected. Immunohistochemistry indicated negative staining for the B subunit of SDH (SDHB) in the resected specimen, leading to a final diagnosis of SDHB-deficient RCC. Genetic testing for SDHB showed a RCC germline variant in exon 6 (NM_003000.3:c.642 G > C) that was previously reported but associated with a novel phenotype (i.e., RCC). Twenty-six years prior, her daughter, who was 25 years old at the time, had undergone radical nephrectomy for a pathologic diagnosis of renal oncocytoma of the right kidney; SDHB immunostaining of her daughter's tumor was also negative retrospectively. We confirmed that her daughter carried the germline variant in SDHB exon 6, similar to the patient. The patient had no evidence of disease progression at 15 months after surgery.

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
琥珀酸脱氢酶b缺乏性肾细胞癌伴种系变异一例日本患者:病例报告。
琥珀酸脱氢酶(SDH)缺陷肾细胞癌(RCC)是一种罕见的肾癌。一位75岁的日本女性表现为肉眼血尿。计算机断层扫描显示左肾有两个肿瘤,并予以切除。免疫组织化学显示,切除标本中SDHB亚基(SDHB)呈阴性染色,最终诊断为SDHB缺陷型RCC。SDHB的基因检测显示,在第6外显子(NM_003000.3: C .642 G > C)存在RCC种系变异,这是以前报道过的,但与一种新的表型(即RCC)相关。26年前,她25岁的女儿因病理诊断为右肾嗜瘤细胞瘤接受了根治性肾切除术;女儿肿瘤的SDHB免疫染色也为阴性。我们证实她的女儿携带SDHB外显子6的种系变异,与患者相似。术后15个月患者无疾病进展迹象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Human Genome Variation
Human Genome Variation Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
2.30
自引率
0.00%
发文量
39
审稿时长
13 weeks
期刊最新文献
Genotypes and phenotypes of neurofibromatosis type 1 patients in Japan: A Hereditary Tumor Cohort Study. CFAP43 variant in persistent respiratory symptoms after hematopoietic cell transplantation. A case of CDKL5 deficiency disorder with a novel intragenic multi-exonic duplication. A mild case of Cockayne syndrome with a novel start-loss variant of ERCC8. Challenges in classifying human chromosomal heteromorphisms using banding cytogenetics: From controversial guidelines to the need for a universal scoring system.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1