Literature DB >> 1811423

Vagal paragangliomas: a report of nine cases.

C Eriksen1, H Girdhar-Gopal, L D Lowry.   

Abstract

Vagal paragangliomas are rare tumors of neural crest origin: fewer than 175 cases have been reported in the English literature. This slow-growing tumor occurs most often at the base of the skull in the parapharyngeal space, but may arise anywhere along the course of the vagus nerve and its branches. Nine clinical presentations and the surgical outcome in seven patients with vagal paragangliomas treated at our institution are reported. A review of the literature, emphasizing evaluation and treatment of these potentially fatal neoplasms, is discussed. Surgical removal is the treatment of choice with vagal tumors. Complications related to the ablation or injury of cranial nerves IX, X, XI, and XII are commonly seen. Surgical techniques that may prevent injury to these vital neural structures are outlined. The postoperative treatment of patients with impaired deglutition secondary to multiple cranial neuropathies is discussed.

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Year:  1991        PMID: 1811423     DOI: 10.1016/0196-0709(91)90006-2

Source DB:  PubMed          Journal:  Am J Otolaryngol        ISSN: 0196-0709            Impact factor:   1.808


  3 in total

Review 1.  The biology and pathology of selected skull base tumors.

Authors:  L Barnes; S B Kapadia
Journal:  J Neurooncol       Date:  1994       Impact factor: 4.130

2.  An unusual cause of reflex cardiovascular syncope: vagal paraganglioma.

Authors:  Ertan Okmen; Izzet Erdinler; Enis Oguz; Ahmet Akyol; Nese Cam
Journal:  Ann Noninvasive Electrocardiol       Date:  2003-04       Impact factor: 1.468

3.  Management of vagal paragangliomas: review of 17 patients.

Authors:  Ricardo González-Orús Álvarez-Morujo; Miguel Arístegui Ruiz; Carlos Martin Oviedo; Itziar Álvarez Palacios; Bartolomé Scola Yurrita
Journal:  Eur Arch Otorhinolaryngol       Date:  2014-06-29       Impact factor: 2.503

  3 in total

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