Literature DB >> 2845333

Glomus vagale tumors.

J Davidson1, P Gullane.   

Abstract

We present a case of a multicentric chemodectoma, with the unusual combination of a glomus vagale and a glomus tympanicum tumor. Multicentricity was suspected before selective carotid arteriography. Our patient, although asymptomatic, had elevated levels of urinary catecholamines preoperatively, which returned to normal postoperatively, suggesting biochemical activity of the tumor. Intraoperative hemostasis was assisted by the use of preoperative selective embolization of the tumor mass and the peripheral location of the injected Ivalon was confirmed histologically. The vagus nerve was anatomically spared and complete function was restored within 10 months. The asymptomatic small glomus tympanicum tumor was treated with embolization alone, as the patient chose to defer treatment at this time, but only time will reveal the effectiveness of this method of management.

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Year:  1988        PMID: 2845333     DOI: 10.1177/019459988809900113

Source DB:  PubMed          Journal:  Otolaryngol Head Neck Surg        ISSN: 0194-5998            Impact factor:   3.497


  3 in total

1.  Surgical therapy of glomus vagale tumors.

Authors:  J D Browne; U Fisch; A Valavanis
Journal:  Skull Base Surg       Date:  1993

2.  Endovascular embolization of paragangliomas: A safe adjuvant to treatment.

Authors:  J Bradley White; Michael J Link; Harry J Cloft
Journal:  J Vasc Interv Neurol       Date:  2008-04

3.  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 in total

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