Wydanie 4/2012
str. 75

Fałdy siatkówki u 11-letniego chłopca z nerwiakowłókniakowatością typu 1. – opis przypadku

Retinal Folds in 11-year-old Boy with Neurofibromatosis 1 – Case Report

Anna Wyszyńska, Paweł Bieliński, Monika Jasielska, Jerzy Mackiewicz

Klinika Chirurgii Siatkówki i Ciała Szklistego Uniwersytetu Medycznego w Lublinie
Kierownik: dr hab. n. med. Jerzy Mackiewicz


Summary: etinal folds can be congenital or acquired. Congenital retinal folds occur in some disorders in developing of the vitreous or/and neurosensory retina. Acquired folds may co-exist with numerous eye conditions such as: hypotony, scleritis, uveal effusion syndrome, retinal detachment, scleral buckling or intravitreous gas injection.
n children retinal folds may occur in association with retinopathy of prematurity or toxocariasis.
The purpose of our work is the case report of 11-year-old boy with neurofibromatosis type 1 with co-existing retinal folds of the left eye. Best corrected visual acuity of both eyes was 1.0. The biomicroscopic evaluation revealed Lisch nodules on the iris and radial folds extending from the disc to the macula in the left eye. Optical coherent tomography confirmed retinal folds, that should be differentiated from choroidal folds. Visual field and ultrasound B showed no abnormalities. Also magnetic resonance was taken to exclude the intraorbital mass that was the biggest fear. All of the additional medical examinations did not give the answer what is the reason of retinal folds.
Neurofibromatosis progresses with the growth of young organism and can develop eye and systemic complication therefore the boy is still under our hospital follow-up.

Słowa kluczowe: NF 1, choroba Recklinghausena, fałdy siatkówki.

Keywords: NF 1, choroba Recklinghausena, fałdy siatkówki.


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