Update on Pheochromocytoma and Paraganglioma from the SSO Endocrine/Head and Neck Disease-Site Work Group. Part 1 of 2: Advances in Pathogenesis and Diagnosis of Pheochromocytoma and Paraganglioma.

Update on Pheochromocytoma and Paraganglioma from the SSO Endocrine/Head and Neck Disease-Site Work Group. Part 1 of 2: Advances in Pathogenesis and Diagnosis of Pheochromocytoma and Paraganglioma.
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DOI:
10.1245/s10434-020-08220-3
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发表时间:
2020-05
影响因子:
3.7
通讯作者:
Kim LT
Kim LT
中科院分区:
医学2区
文献类型:
--
作者:
Patel D;Phay JE;Yen TWF;Dickson PV;Wang TS;Garcia R;Yang AD;Solórzano CC;Kim LT

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这是两部分回顾嗜铬细胞瘤和副神经节瘤(PPGLs)的第一部分,涉及临床表现,诊断,管理,治疗和结果。在这第一部分,流行病学,患病率,遗传病因,临床表现,生化和放射检查进行了讨论。特别强调了PPGL遗传学的最新进展以及对所有PPGL患者进行基因检测的建议。最后,讨论并强调了评估PPGLs的最新成像方法。
This first part of a two-part review of pheochromocytoma and paragangliomas (PPGLs) addresses clinical presentation, diagnosis, management, treatment, and outcomes. In this first part, the epidemiology, prevalence, genetic etiology, clinical presentation, and biochemical and radiologic workup are discussed. In particular, recent advances in the genetics underlying PPGLs and the recommendation for genetic testing of all patients with PPGL are emphasized. Finally, the newer imaging methods for evaluating of PPGLs are discussed and highlighted.
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