A rare case of familial carotid body tumor in a patient with bilateral fibromuscular dysplasia

被引：5

作者：

Han, Daniel K. ^{[1
]}

Fishman, Eric W. ^{[1
]}

Walkup, Maggie H. ^{[1
]}

Olin, Jeffrey W. ^{[2
,3
]}

Marin, Michael L. ^{[1
]}

Faries, Peter L. ^{[1
]}

机构：

[1] Mt Sinai Sch Med, Div Vasc Surg, New York, NY USA

[2] Mt Sinai Sch Med, Zena & Michael A Wiener Cardiovasc Inst, New York, NY USA

[3] Mt Sinai Sch Med, Marie Josee & Henry R Kravis Ctr Cardiovasc Hlth, New York, NY USA

来源：

JOURNAL OF VASCULAR SURGERY | 2010年 / 52卷 / 03期

关键词：

FOLLOW-UP; PARAGANGLIOMAS; DISEASE; MANAGEMENT; ARTERY; BRAIN; NECK; HEAD;

D O I：

10.1016/j.jvs.2010.04.028

中图分类号：

R61 [外科手术学];

学科分类号：

摘要：

Carotid body tumors (CBTs) are neuroendocrine tumors that arise due to mutations of respiratory cycle enzymes. Fibromuscular dysplasia (FMD) is a disease that causes narrowing of medium-sized arteries. There is no documented link between CBT and FM D. In this article, we report a case of a patient with bilateral carotid FM D and familial CBT, including one in an identical twin who underwent successful surgical excision of the CBT. We describe specific considerations in the management of CBT in patients with concomitant carotid FM D. Also, we review the literature about the genetics of familial CBT and its possible relationship to the etiology of FMD. (J Vase Surg 2010;52:746-50.)

引用

页码：746 / 750

页数：5

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