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Revista Mexicana de Oftalmología

Anales de la Sociedad Mexicana de Oftalmología y Archivos de la Asociación Para Evitar la Ceguera en México
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2007, Number 2

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Rev Mex Oftalmol 2007; 81 (2)

Neurofibromatosis orbitopalpebral. Reporte de un caso

Alvarez-Hermosa J, Meléndez A, Salcedo–Casillas G
Full text How to cite this article

Language: Spanish
References: 3
Page: 114-116
PDF size: 98.22 Kb.


Key words:

Type 1 neurofibromatosis, orbitopalpebral plexiform neurofibroma, surgical treatment.

ABSTRACT

Orbitopalpebral neurofibromatosis is a debilitating disease and can be part of type 1 neurofibromatosis. The orbitopalpebral neurofibroma produces an aesthetic a functional problem, has a rapid phase of growth during childhood and puberty, infiltrating orbital bland tissues, including the extra ocular muscles and the lachrymal gland. The enormous overgrowth of the orbital peripheral nerves leads to an enlarged orbit and excessive redundancy of the lid skin.
The report describes the case of a patient with an orbitopalpebral plexiform neurofibroma since birth, with a progressive increase of volume and important aesthetic and functional changes. The employed therapeutic procures a cosmetic improvement to facilitate the patient’s integration in the society.


REFERENCES

  1. Marchac D, Britto J. Remodelling the upper eyelid in the management of orbitopalpebral neurofibromatosis. Brit J Plastic Surg 2005, 58(7):944-956.

  2. Lee V, Ragge N. The surgical management of childhood orbitotemporal neurofibromatosis. Brit J Plastic Surg 2003; 56(4):380-387.

  3. Lee V, Ragge N. Orbitotemporal neurofibromatosis; Clinical features and surgical management. Ophthalmology 2004;111(2):382-388.




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Rev Mex Oftalmol. 2007;81