Oman Journal of Ophthalmology. 2009; 2 (2): 82-85
Dans Anglais
| IMEMR
| ID: emr-102743
ABSTRACT
Von Hippel-Lindau [VHL] disease is a rare multisystem familial tumor syndrome of autosomal dominant inheritance. Hallmark lesions include retinal, cerebellum and spinal cord hemangioblastomas, renal cell carcinomas, adrenal pheochromocytomas, angiomatous or cystic lesions of the kidneys, pancreas, and epididymis. We report a case of VHL disease in a 26-year-old patient who presented with exudative macular edema. Ocular and systemic studies revealed the presence of retinal and central nervous system hemangioblastomas, adrenal pheochromocytoma, multiple pancreatic, and kidney cysts. The retinal angiomas were successfully treated with argon laser photocoagulation and cryotherapy
Recherche sur Google
Indice:
Méditerranée orientale
Sujet Principal:
Angiographie fluorescéinique
/
Oedème maculaire
/
Coagulation par laser
/
Hémangioblastome
/
Cryothérapie
/
Lasers à excimères
/
Maladie de von Hippel-Lindau
/
Dégénérescence maculaire
Type d'étude:
Enquête cas-témoins / Études cas/témoins
Limites du sujet:
Humains
/
Mâle
langue:
Anglais
Texte intégral:
Oman J. Ophthalmol.
Année:
2009
Documents relatifs à ce sujet
MEDLINE
...
LILACS
LIS