Hereditary leiomyomatosis and renal cell carcinoma: very early diagnosis of renal cancer in a paediatric patient

被引:43
作者
Alrashdi, Ismail [1 ]
Levine, Samantha [2 ]
Paterson, Joan [3 ]
Saxena, Rohit [4 ]
Patel, Soonie R. [4 ]
Depani, Sarita [5 ]
Hargrave, Darren R. [5 ]
Pritchard-Jones, Kathy [5 ]
Hodgson, Shirley V. [1 ]
机构
[1] St George Hosp, Sch Med, Dept Med Genet, London SW17 0RE, England
[2] St Georges Healthcare Trust, Dept Cellular Pathol, London, England
[3] Addenbrookes Hosp, Addenbrookes Treatment Ctr, Cambridge, England
[4] Mayday Univ Hosp, Dept Paediat, Croydon, England
[5] Royal Marsden Hosp, Paediat Oncol Unit, Sutton, Surrey, England
关键词
Papillary type 2 renal cell carcinoma; Fumarate hydratase; Cutaneous leiomyomatosis; Uterine leiomyomatosis; Hereditary leiomyomatosis; HLRCC; FUMARATE HYDRATASE MUTATIONS; UTERINE LEIOMYOMAS; FH; DEFICIENCY; FIBROIDS; SPECTRUM; FAMILIES; TUMORS; RISK;
D O I
10.1007/s10689-009-9306-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hereditary leiomyomatosis and renal cell cancer is a hereditary cancer syndrome in which affected individuals are at risk for cutaneous and uterine leiomyomas, and renal cancer. Previous reports have stressed the aggressiveness of the renal tumours, often with early metastasis, despite small primary tumour size. Almost all the previously reported patients were adults, and different studies showed variability in penetrance for the renal tumours. We report a patient in whom renal cancer was detected at the age of 11 years at his first routine screening imaging after he was found to carry a fumarate hydratase gene mutation (c.1189G > A) transmitted from his mother. This report serves to emphasize the need to improve guidelines for screening of at risk individuals, including the necessity for predictive genetic testing and early institution of tumour surveillance in childhood.
引用
收藏
页码:239 / 243
页数:5
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