Malignant paraganglioma caused by a novel germline mutation of the succinate dehydrogenase D-gene - A case report

被引:13
作者
Papaspyrou, Konstantinos [1 ]
Rossmann, Heidi [2 ]
Fottner, Christian [3 ]
Weber, Matthias M. [3 ]
Mann, Wolf [1 ]
Lackner, Karl J. [2 ]
Helling, Kai [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Sch Med, Dept Otorhinolaryngol, Mainz, Germany
[2] Johannes Gutenberg Univ Mainz, Sch Med, Dept Clin Chem & Lab Med, Mainz, Germany
[3] Johannes Gutenberg Univ Mainz, Sch Med, Div Endocrinol & Metab, Dept Internal Med 1, Mainz, Germany
来源
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK | 2008年 / 30卷 / 07期
关键词
malignant paraganglioma; heredity; succinate dehydrogenase; (18)FIuoro-Dopa-PET; pheochromocytoma;
D O I
10.1002/hed.20746
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background. Paragangliomas of the head and neck are rare, mostly benign tumors. Approximately 10% to 15% of paragangliomas are caused by mutations in the succinate dehydrogenase (SDH) genes B, C, or D. These are often multifocal as part of paraganglioma syndromes and hormone secreting, and malignant particularly associated with mutations in SDHB. Methods and Results. A 29-year-old man was seen with recurrent paraganglioma. The patient's father reportedly suffered from bilateral carotid body tumors. Imaging studies showed metastases in both lungs and the liver. There was no increased hormone production by the tumor. Sequence analysis of the SDH genes revealed a novel C to T nonsense mutation in the first exon of the SDHD gene (R17X). Conclusions. A novel mutation in the SDHD gene associated with malignant paraganglioma is reported. This case underscores the relevance of family history and genetic analysis, thus permitting early detection of unaffected carriers. These have to be monitored clinically, biochemically and by imaging techniques. (c) 2008 Wiley Periodicals, Inc.
引用
收藏
页码:964 / 969
页数:6
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