SDH-deficient renal cell carcinoma: A case report associated with a novel germline mutation

被引：6
|
作者：
Milionis, Vassilis [1 ]
Goutas, Dimitrios [2 ]
Vlachodimitropoulos, Dimitrios [1 ,3 ]
Katsoulas, Nikolaos [2 ]
Kyriazis, Iason D. [4 ]
Liatsikos, Evangelos N. [4 ]
Marinakis, Nikolaos [5 ]
Joanne, Traeger-Synodinos [5 ]
Lazaris, Andreas C. [2 ]
Goutas, Nikolaos [1 ,3 ]
机构：
[1] Istomedica SA, Athens, Greece
[2] Natl & Kapodistrian Univ Athens, Laikon Gen Hosp Athens, Sch Med, Dept Pathol 1, Mikras Asias 75A, Athens 11527, Greece
[3] Natl & Kapodistrian Univ Athens, Lab Forens Med & Toxicol, Athens, Greece
[4] Univ Patras, Dept Urol, Patras, Greece
[5] Natl & Kapodistrian Univ Athens, St Sophia Childrens Hosp, Lab Med Genet, Athens, Greece
来源：
CLINICAL CASE REPORTS | 2021年 / 9卷 / 10期
关键词：
nephrology; renal cell carcinoma; succinate dehydrogenase deficiency; urology; SUCCINATE-DEHYDROGENASE; COMPLEX II; UNIQUE SUBTYPE; TUMORS; PARAGANGLIOMA; GENE; PHEOCHROMOCYTOMA;
D O I：
10.1002/ccr3.4605
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
The highly syndromic nature of succinate dehydrogenase-deficient RCCs constitutes their active surveillance and molecular profiling the alpha and omega.
引用
收藏
页数：10
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