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一名8岁儿童的与琥珀酸脱氢酶亚基B相关的恶性副神经节瘤:首次筛查的年龄?

Malignant paraganglioma associated with succinate dehydrogenase subunit B in an 8-year-old child: the age of first screening?

作者信息

Prodanov Tamara, Havekes Bas, Nathanson Katherine L, Adams Karen T, Pacak Karel

机构信息

Reproductive and Adult Endocrinology Program, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892-1109, USA.

出版信息

Pediatr Nephrol. 2009 Jun;24(6):1239-42. doi: 10.1007/s00467-008-1111-8. Epub 2009 Feb 3.

Abstract

Several studies have shown that patients with succinate dehydrogenase subunit B (SDHB) mutations have a very high risk for developing malignant paragangliomas. However, there is no consensus of what age screening for paragangliomas should start. We report a case of an 8-year-old white girl with a 3-year history of catecholamine excess-related complaints who was diagnosed with a malignant SDHB-associated mediastinal paraganglioma. The patient presented with intermittent sweating, headache, nausea, vomiting, fatigue and weight loss that had been present since she was 5 years of age. A large posterior mediastinal mass measuring 6.4 cm x 3.1 cm x 4.6 cm was discovered on computed tomography (CT) and magnetic resonance imaging (MRI). Laboratory data included an elevated level of urine normetanephrine of 45,400 microg/g creatinine (upper reference limit 718 microg/g) and elevated level of plasma normetanephrine of 62.4 nmol/l (upper reference limit <0.90 nmol/l). She was diagnosed with a thoracic paraganglioma and subsequently underwent surgical removal of the tumor and two lymph nodes. Histopathologic examination confirmed metastatic paraganglioma. Postoperatively, her blood pressure normalized and plasma normetanephrine levels remained normal. Our patient first presented with paraganglioma-associated signs and symptoms at the young age of 5 years. This case clearly illustrates the need for increased vigilance and screening for paragangliomas in families with SDHB at a younger age than previously thought.

摘要

多项研究表明,琥珀酸脱氢酶亚基B(SDHB)突变的患者发生恶性副神经节瘤的风险非常高。然而,对于副神经节瘤筛查应从什么年龄开始,目前尚无共识。我们报告一例8岁白人女孩,有3年与儿茶酚胺过量相关症状的病史,被诊断为与SDHB相关的恶性纵隔副神经节瘤。该患者自5岁起就出现间歇性出汗、头痛、恶心、呕吐、疲劳和体重减轻。计算机断层扫描(CT)和磁共振成像(MRI)发现一个位于后纵隔的大肿块,大小为6.4 cm×3.1 cm×4.6 cm。实验室检查数据包括尿去甲变肾上腺素水平升高至45400μg/g肌酐(参考上限718μg/g),血浆去甲变肾上腺素水平升高至62.4 nmol/l(参考上限<0.90 nmol/l)。她被诊断为胸段副神经节瘤,随后接受了肿瘤及两个淋巴结的手术切除。组织病理学检查证实为转移性副神经节瘤。术后,她的血压恢复正常,血浆去甲变肾上腺素水平保持正常。我们的患者在5岁时就首次出现与副神经节瘤相关的体征和症状。该病例清楚地表明,对于有SDHB突变的家庭,需要比以前认为的更年轻的年龄就提高对副神经节瘤的警惕并进行筛查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af4/4714580/aa3dceaf94f9/nihms750188f1.jpg

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