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遗传性平滑肌瘤病和肾细胞癌:儿科患者肾癌的极早期诊断。

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

机构信息

Department of Medical Genetics, St George's Hospital Medical School, Cranmer Terrace, SW17 0RE, London, UK.

出版信息

Fam Cancer. 2010 Jun;9(2):239-43. doi: 10.1007/s10689-009-9306-0.

Abstract

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.

摘要

遗传性平滑肌瘤病和肾细胞癌是一种遗传性癌症综合征,受影响的个体有患皮肤和子宫平滑肌瘤以及肾癌的风险。以前的报告强调了肾肿瘤的侵袭性,尽管原发肿瘤较小,但常伴有早期转移。几乎所有以前报告的患者都是成年人,不同的研究显示肾肿瘤的外显率存在差异。我们报告了一例患者,在发现携带琥珀酸氢酶基因突变(c.1189G > A)后,他在首次常规筛查成像时于 11 岁时被诊断为肾癌,该基因突变是从他母亲那里遗传的。本报告旨在强调需要改进高危人群的筛查指南,包括进行预测性基因检测和在儿童期早期进行肿瘤监测的必要性。

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