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Anales de Otorrinolaringología Mexicana

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2010, Number 4

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Otorrinolaringología 2010; 55 (4)

Polysomnographic characteristics of the sleep obstructive apnea syndrome caused by a nasopharyngeal juvenile angiofibroma

Labra A, Galicia PL, Huerta DÁD, Arceo TM, Haro VR
Full text How to cite this article

Language: Spanish
References: 5
Page: 143-145
PDF size: 288.77 Kb.


Key words:

juvenile angiofibroma, polysomnography, obstructive sleep apnea syndrome.

ABSTRACT

Juvenile angiofibroma is an uncommon neoplasm arising at the nasopharynx of male children, which can erode the bone at the skull base as it grows, getting easily into the cranial cavity. It can also produce a mass-effect in the pharynx, so the patient may develope an obstructive sleep apnea syndrome. We present the features of this two associated conditions.


REFERENCES

  1. Labra A, Chavolla MR, Lopez UA, Alanis CJ, et al. Flutamide as a preoperative treatment in juvenile angiofibroma (JA) with intracranial invasion: report of 7 cases. Otolaryngol Head Neck Surg 2004;130(4):466-469.

  2. Salib RJ, Sadek SA, Dutt SN, Pearman K. Antrochoanal polyp presenting with obstructive sleep apnoea and cachexia. Int J Pediatr Otorhinolar 2000;54:163-166.

  3. Chandler JR, Goulding R, Moskowitz L, Quencer RM. Nasopharyngeal angiofibromas: staging and management. Ann Otol Rhinol Laryngol 1984;93:322-329.

  4. Shibata N, Nishimura T, Morishima N, Hasegawa K, et al. A case of sleep apnea syndrome due to a nasopharyngeal tumor (en japonés). Nippon Jibiinkoka Gakkai Kaiho 1996;99(1):6-12.

  5. Kato M, Roberts TP, Phillips BG, Haynes WG, et al. Impairment of endothelium-dependent vasodilation of resistance vessels in patients with obstructive sleep apnea. Circulation 2000;102:2607-2610.




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Otorrinolaringología. 2010;55