大腹膜后副神经节瘤与琥珀酸脱氢酶基因的种系突变相关。

IF 1.9 Q3 ONCOLOGY
Journal of Kidney Cancer and VHL Pub Date : 2021-01-25 eCollection Date: 2021-01-01 DOI:10.15586/jkcvhl.v8i1.129
Wen Min Chen, Philip Olson, Rohith Arcot, Huy Nguyen, Faisal Quereshi, Courtney Kokenakes, Michael L Cher
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引用次数: 2

摘要

副神经节瘤(PGLs)是一种罕见的神经肿瘤,可良性或恶性,通常与家族综合征有关。我们提出一个23岁的男性与一个大的腹膜后PGL偶然发现在检查期间升高的肝酶。手术切除后,患者发现琥珀酸脱氢酶B (SDHB)基因常染色体显性突变,与散发性pgl或其他家族综合征相比,该突变与肿瘤复发、隐匿转移和其他癌症发展的高风险相关。建议患者的一级亲属进行基因突变筛查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Large Retroperitoneal Paraganglioma Associated with Germline Mutation of the Succinate Dehydrogenase Gene.

Large Retroperitoneal Paraganglioma Associated with Germline Mutation of the Succinate Dehydrogenase Gene.

Large Retroperitoneal Paraganglioma Associated with Germline Mutation of the Succinate Dehydrogenase Gene.

Large Retroperitoneal Paraganglioma Associated with Germline Mutation of the Succinate Dehydrogenase Gene.

Paragangliomas (PGLs) are rare neural tumors that can be benign or malignant and often associated with familial syndromes. We present a case of a 23-year-old male with a large retroperitoneal PGL found incidentally during the workup of elevated liver enzymes. After surgical excision, the patient was found to have an autosomal dominant mutation in the succinate dehydrogenase B (SDHB) gene, which when compared to sporadic PGLs or other familial syndromes is associated with a higher risk of tumor recurrence, occult metastasis, and development of other cancers. The patient's first-degree relatives were recommended to undergo screening for the genetic mutation.

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