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Head and neck paragangliomas

✍ Scribed by Mendenhall, William M. (author);Amdur, Robert J. (author);Vaysberg, Mikhail (author);Mendenhall, Charles M. (author);Werning, John W. (author)


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
79 KB
Volume
33
Category
Article
ISSN
1043-3074

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Head and neck paragangliomas
✍ Mendenhall, William M. (author);Amdur, Robert J. (author);Vaysberg, Mikhail (aut πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 English βš– 79 KB

## Abstract ## Background The purpose of this study was to describe the natural history and optimal treatment for head and neck paragangliomas (PGs). ## Methods Our methods were the review of the pertinent literature. ## Results PGs are rare tumors seen most commonly in the head and neck. Appr

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## Abstract ## Background. Head and neck paragangliomas (PGL) are rare, mostly benign tumors. About 10% to 15% of PGL are caused by mutations in the succinate dehydrogenase genes B, C, or D and may appear multifocally. ## Methods and Results. A retrospective review of 120 patients with 146 head

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Objectives/Hypothesis: To describe a novel germline mutation in the succinate dehydrogenase subunit B (SDHB) gene. Study Design: Retrospective review. Methods: The medical records of a patient with bilateral carotid body paragangliomas were reviewed. Results: A 35-year-old woman with a family hist

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## Abstract ## Background Paragangliomas are highly vascular tumors of neural crest origin that involve the walls of blood vessels or specific nerves within the head and neck. They may be multicentric, and they are rarely malignant. Surgery is the preferred treatment, and these tumors frequently e

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## Abstract ## BACKGROUND Malignant paragangliomas of the head and neck are rare, with previous reports limited to nine or fewer patients. The current review included 59 cases extracted from the National Cancer Data Base that were diagnosed between 1985–1996. ## METHODS The primary criterion fo