An apparently sporadic paraganglioma with an SDHB gene germline mutation presenting at age 68 years

被引:6
作者
Elston, MS
Benn, D
Robinson, BG
Conaglen, JV
机构
[1] Waikato Hosp, Dept Endocrinol, Hamilton, New Zealand
[2] Univ Sydney, Kolling Inst Med Res, Sydney, NSW 2006, Australia
[3] Royal N Shore Hosp, Sydney, NSW, Australia
关键词
paraganglioma; phaeochromocytoma; SDHB;
D O I
10.1111/j.1445-5994.2006.01023.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Paragangliomas (PGLs) are rare tumours arising from parasympathetic-associated paraganglia (particularly of the head and neck) or from sympathetic-associated paraganglia such as in the adrenal medulla when they are termed phaeochromocytomas and at extra-adrenal sites in the abdomen and thorax. Recent reports have found frequent germline mutations of VHL, RET, SDHB or SDHD not only in familial cases but also in apparently sporadic cases of phaeochromocytoma. These germline mutations are particularly likely to be found if multifocal disease is present or if the phaeochromocytoma or PGL occurs at a young age. We report a germline splice site mutation in SDHB in a patient presenting with an incidental, apparently sporadic, abdominal sympathetic PGL at 68 years of age.
引用
收藏
页码:129 / 131
页数:3
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