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Bilateral diffuse iris nodular nevi. Clinical and histopathologic characterization
Ophthalmology
|March 1, 1995
Summary
Bilateral diffuse iris nodular nevi are a rare condition presenting as multiple iris excrescences. This study describes 30 patients and their associations with various congenital anomalies.
Area of Science:
- Ophthalmology
- Developmental Biology
- Genetics
Background:
- Diffuse nodular nevus of the iris is an uncommon condition characterized by multiple verrucous excrescences on the iris surface.
- This study presents the largest clinical series to date of bilateral diffuse iris nodular nevi.
Observation:
- Thirty patients with bilateral diffuse iris nodular nevi were analyzed.
- Associated conditions included congenital cataract, neurofibromatosis, oculodermal melanocytosis, congenital ptosis, and various ocular anomalies (Morning Glory, Axenfeld, Peters).
Findings:
- Iris nodules were uniformly sized, brown, and diffusely distributed.
- Microscopy revealed plaques of nevoid cells interwoven with uveal melanocytes, suggesting a neural crest developmental variant.
Implications:
- Bilateral diffuse iris nodular nevi represent a distinct entity, potentially a variant of neural crest development.
- These nodules are clinically distinct from Lisch nodules and other pathological iris lesions.
- No ocular complications were directly attributed to the iris nodules themselves.