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尿路和骨肿瘤的家族聚集性:探寻一种综合征。

Familial aggregation of urinary tract and bone tumors: searching for a syndrome.

作者信息

Frings Andreas, Geigl Jochen B, Liegl-Atzwanger Bernadette, Leithner Andreas

机构信息

Department of Orthopedic Surgery, Medical University of Graz, Auenbruggerplatz 5, 8036 Graz, Austria.

出版信息

Case Rep Med. 2012;2012:107894. doi: 10.1155/2012/107894. Epub 2012 May 20.

Abstract

Positive family anamnesis is an important risk factor for cancer, and therefore further investigations need to be done if familial aggregation of cancer is observed. Due to a rare combination of urinary tract and bone tumors occurring in the family presented herein we hypothesized a hereditary predisposition and thus, Li-Fraumeni syndrome was considered to be the most likely differential diagnosis. To confirm Li-Fraumeni syndrome, we set out to investigate this case by analyzing the tumor suppressor gene p53. However, taking into account all the diagnostic results obtained, Li-Fraumeni syndrome could not be confirmed, but there is still uncertainty regarding a definitive diagnosis.

摘要

阳性家族史是癌症的一个重要风险因素,因此,如果观察到癌症的家族聚集现象,就需要进一步进行调查。由于本文所呈现的家族中出现了罕见的尿路和骨肿瘤组合,我们推测存在遗传易感性,因此,李-弗劳梅尼综合征被认为是最有可能的鉴别诊断。为了确诊李-弗劳梅尼综合征,我们着手通过分析肿瘤抑制基因p53来调查此病例。然而,综合所有获得的诊断结果,无法确诊李-弗劳梅尼综合征,但对于最终诊断仍存在不确定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8865/3362849/3555cd25d43a/CRIM2012-107894.001.jpg

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