Fumarate hydratase c.914T > C (p.Phe305Ser) is a pathogenic variant associated with hereditary leiomyomatosis and renal cell cancer syndrome

被引:0
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作者
Breen, Kelsey E. [1 ]
Carlo, Maria I. [1 ]
Kemel, Yelena [2 ]
Maio, Anna [1 ]
Chen, Ying-Bei [3 ]
Zhang, Liying [4 ]
Ceyhan-Birsoy, Ozge [3 ]
Mandelker, Diana [3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, 1275 York Ave, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Niehaus Ctr Inherited Canc Genom, Sloan Kettering Inst, 1275 York Ave, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Pathol, 1275 York Ave, New York, NY 10021 USA
[4] Univ Calif Los Angeles, Dept Pathol & Lab Med, Los Angeles, CA USA
来源
关键词
carcinoma; fumarate hydratase; leiomyomatosis; mutation; renal cell; GERMLINE MUTATIONS; CARCINOMA SYNDROME; UTERINE FIBROIDS; FH; FAMILIES; SUSCEPTIBILITY; SURVEILLANCE; GENETICS; SPECTRUM; FEATURES;
D O I
10.1002/mgg3.1293
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Hereditary leiomyomatosis and renal cell cancer syndrome (HLRCC), caused by heterozygous germline pathogenic variants in the FH, confers an increased risk for cutaneous and uterine leiomyomas and renal cancer. Methods About 13,722 advanced cancer patients, including 560 with renal cell carcinoma, had germline analysis performed in the context of tumor-normal sequencing under an IRB approved protocol. Results We report two unrelated individuals with early onset kidney cancer who both carried the c.914C > T (p.Phe305Ser) germline variant in the FH. Both tumors exhibited loss of FH staining by immunohistochemistry and/or positive 2SC staining. Subsequent familial testing discovered that a daughter of a proband who carried the variant had both cutaneous and uterine leiomyomas. Conclusion This combination of evidence suggests that the FH c.914C > T (p.Phe305Ser) is pathogenic for HLRCC.
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页数:7
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