2017
DOI: 10.1016/j.ijscr.2017.11.019
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Bilateral carotid body tumor resection in a female patient

Abstract: HighlightsCarotid body tumors are rare neuroendocrine neoplasms derived from neural crest cells.MRI imaging is considered to be the gold standard criterion for carotid body tumors diagnosis.Surgical resection of carotid body tumors represents a special challenge to the surgeon.

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Cited by 17 publications
(10 citation statements)
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“…2,3 The onset of CBTs is sporadic, usually occurring at 40-60 years of age in women, among whom CBTs are more prevalent. While most cases are sporadic, 15% are familial or proliferative when associated with chronic hypoxia (CH), 4,5 and most are unilateral, benign masses. 6,7 Because CBT is rare, most studies have been case reports or single-center treatment experience summaries.…”
Section: Introductionmentioning
confidence: 99%
“…2,3 The onset of CBTs is sporadic, usually occurring at 40-60 years of age in women, among whom CBTs are more prevalent. While most cases are sporadic, 15% are familial or proliferative when associated with chronic hypoxia (CH), 4,5 and most are unilateral, benign masses. 6,7 Because CBT is rare, most studies have been case reports or single-center treatment experience summaries.…”
Section: Introductionmentioning
confidence: 99%
“…Gross total resection (GTR) is the gold standard for resectable CBTs in healthy patients due to risks of damage to local structures and risk of metastatic disease if left untreated ( Burgess et al 2017 ). Complete tumor regression with RT or chemotherapy alone is rare ( Mendenhall et al 2001 ).…”
Section: Introductionmentioning
confidence: 99%
“…La incidencia de los TCC se ha descrito aproximadamente en 1 de cada 30,000-100,000 habitantes, por lo que las neoplasias son poco comunes, sin embargo, representan más de la mitad de los paragangliomas que corresponden a la zona de cabeza y cuello 2 . Nueve de cada diez casos ocurren esporádicamente, el resto son hereditarios, en donde se han reportado cerca de 1/3 de TCC bilaterales (menos del 5% del total de casos) 5,6 . Se han identificado alrededor de seis genes asociados al posible desarrollo de feocromocitomas/paragangliomas 4 .…”
Section: Introductionunclassified