Portal de Periódicos da CAPES

Hamartomas of the Iris and Ciliary Epithelium in Tuberous Sclerosis Complex

2000; American Medical Association; Volume: 118; Issue: 5 Linguagem: Inglês

10.1001/archopht.118.5.711

1538-3601

Ralph C. Eagle,

Genetic and Kidney Cyst Diseases

Astrocytic hamartomas of the retina are the principal ocular manifestation of tuberous sclerosis complex. Iris abnormalities are rare in tuberous sclerosis complex and include focal areas of stromal depigmentation and atypical colobomata. We describe 2 patients who were found on histopathological examination to have lesions consistent with hamartomas of the iris pigment epithelium and ciliary body epithelium. Iris abnormalities, including pupillary irregularities, were noted on clinical examination prior to the development of iris neovascularization in both patients. These observations suggest that iris abnormalities, including atypical colobomas, may be caused by hamartomas of the iris pigment epithelium and ciliary epithelium in some patients with tuberous sclerosis complex. To our knowledge, hamartomas of tissues derived from the anterior part of the neuroectodermal optic cup have not been reported in cases of tuberous sclerosis complex.