RESUMEN
Tuberous sclerosis is a genetic disease with autosomal dominant inheritance, associated with hamartomas in several organs and various skin findings. A case of a ten year old boy is presented here to highlight the multisystem involvement in tuberous sclerosis. The child had seizures, facial papular naevi and peri-ungual fibromas. MRI revealed cortical tubers, white matter lesions and subependymal nodules. Orbital ultrasound showed retinal hamartoma on the left side. Ultrasound of the abdomen revealed a soft tissue mass at the upper pole of left kidney with a small cyst in right kidney.
Asunto(s)
Encéfalo/patología , Niño , Diagnóstico Diferencial , Cara , Fibroma/patología , Hamartoma/diagnóstico , Humanos , Riñón/patología , Masculino , Uñas/patología , Nevo/diagnóstico , Enfermedades de la Retina/diagnóstico , Convulsiones/etiología , Neoplasias Cutáneas/diagnóstico , Esclerosis Tuberosa/complicacionesRESUMEN
Our experience of the use of Cyanoacrylate glue in 50 cases of perforation or impending perforation of cornea has been presented. The method of application has been described. Quite encouraging and useful results have been obtained.