| Literature DB >> 30122859 |
Jerry A Shields1, Carol L Shields1, Sara E Lally1, Tatyana Milman2, Ralph C Eagle2.
Abstract
An 8-year-old girl was referred for an amelanotic iris tumor believed to have enlarged slightly over 3 months, suspicious for juvenile xanthogranuloma (JXG). The affected right eye had a lightly pigmented, vascular iris mass measuring 6 mm in basal dimension and 2 mm in thickness. There were no feeder vessels, seeding, inflammatory cells, or cutaneous abnormalities. Diagnostic fine needle aspiration biopsy (FNAB) was performed, revealing spindle B melanoma cells that were immunoreactive for melanocytic markers HMB45 and Melan-A. Complete tumor resection by basal sector iridectomy was performed. Histopathology confirmed spindle B melanoma. At 14-years follow up, there has been no recurrence or metastasis and visual acuity remains 20/25. Iris melanoma can develop in children and clinically resemble nodular JXG.Entities:
Keywords: Child; eye; iris; juvenile xanthogranuloma; melanoma; pediatric; tumor
Mesh:
Year: 2018 PMID: 30122859 PMCID: PMC6071340 DOI: 10.4103/meajo.MEAJO_7_18
Source DB: PubMed Journal: Middle East Afr J Ophthalmol ISSN: 0974-9233