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在与SDHD相关的头颈部副神经节瘤患者中通过筛查检测到的嗜铬细胞瘤和肾上腺外副神经节瘤

Pheochromocytomas and extra-adrenal paragangliomas detected by screening in patients with SDHD-associated head-and-neck paragangliomas.

作者信息

Havekes B, van der Klaauw A A, Weiss M M, Jansen J C, van der Mey A G L, Vriends A H J T, Bonsing B A, Romijn J A, Corssmit E P M

机构信息

Department of Endocrinology and Metabolic Diseases, Leiden University Medical Center, 2300 RC Leiden, The Netherlands.

出版信息

Endocr Relat Cancer. 2009 Jun;16(2):527-36. doi: 10.1677/ERC-09-0024. Epub 2009 Mar 16.

Abstract

Patients with SDHD-associated head-and-neck paragangliomas (HNP) are at risk for developing pheochromocytomas for which screening has been advised. To assess clinical, biochemical, and radiological outcomes of screening in a large single-center cohort of SDHD-positive patients with HNP and to address the necessity for repetitive follow-up, we evaluated 93 patients with SDHD-associated HNP (p.Asp92Tyr, p.Leu139Pro). Screening consisted of measurement of 24 h urinary excretion of catecholamines and/or their metabolites in duplicate, which was repeated with intervals of 2 years if initial biochemical screening was negative. In patients, in whom urinary excretion was above the reference limit, imaging studies with (123)I-MIBG (metaiodobenzylguanidine) scintigraphy and magnetic resonance imaging (MRI) and/or computed tomography (CT) were performed. Pheochromocytomas and extra-adrenal paragangliomas were treated surgically after appropriate blockade. Median follow-up was 4.5 years (range 0.5-19.5 years). Twenty-eight out of the 93 patients were included in our study and underwent additional imaging for pheochromocytomas/extra-adrenal paragangliomas. In 11 out of the 28 patients intra-adrenal pheochromocytomas were found. Extra-adrenal paragangliomas were discovered in eight patients. These tumors were detected during initial screening in 63% of cases, whereas 37% were detected after repeated biochemical screening. One patient was diagnosed with a biochemically silent pheochromocytoma. The high prevalence of pheochromocytomas/extra-adrenal paragangliomas in patients with SDHD-associated HNP warrants regular screening for tumors in these patients. Paragangliomas that do not secrete catecholamines might be more prevalent than previously reported. Future studies will have to establish whether routine imaging studies should be included in the screening of SDHD mutation carriers, irrespective of biochemical screening.

摘要

患有与SDHD相关的头颈部副神经节瘤(HNP)的患者有发生嗜铬细胞瘤的风险,因此建议进行筛查。为了评估在一个大型单中心队列中,SDHD阳性HNP患者的筛查的临床、生化和影像学结果,并探讨重复随访的必要性,我们评估了93例与SDHD相关的HNP患者(p.Asp92Tyr,p.Leu139Pro)。筛查包括重复测量24小时尿儿茶酚胺和/或其代谢产物的排泄量,如果初始生化筛查为阴性,则每2年重复一次。对于尿排泄量高于参考限值的患者,进行(123)I-MIBG(间碘苄胍)闪烁显像、磁共振成像(MRI)和/或计算机断层扫描(CT)等影像学检查。嗜铬细胞瘤和肾上腺外副神经节瘤在适当阻滞后进行手术治疗。中位随访时间为4.5年(范围0.5 - 19.5年)。93例患者中有28例纳入我们的研究,并接受了嗜铬细胞瘤/肾上腺外副神经节瘤的额外影像学检查。28例患者中有11例发现肾上腺内嗜铬细胞瘤。8例患者发现肾上腺外副神经节瘤。这些肿瘤在63%的病例中在初始筛查时被检测到,而37%是在重复生化筛查后被检测到。1例患者被诊断为生化隐匿性嗜铬细胞瘤。在与SDHD相关的HNP患者中,嗜铬细胞瘤/肾上腺外副神经节瘤的高患病率表明应对这些患者进行定期肿瘤筛查。不分泌儿茶酚胺的副神经节瘤可能比以前报道的更为普遍。未来的研究将必须确定在SDHD突变携带者的筛查中,无论生化筛查结果如何,是否都应包括常规影像学检查。

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