Iris Melanoma-A Rare Ocular Tumour

Iris Melanoma: Rarity and Diagnostic Challenges
Vol. 20 No. 1 : 2025 (366-374)

Chiun Pei Rong
Chiun Pei Rong
Amelia Lim Lay Suan
Amelia Lim Lay Suan
Nor Azita Ahmad Tarmidzi
Nor Azita Ahmad Tarmidzi
Wan Haslina Wan Abdul Halim
Wan Haslina Wan Abdul Halim
Asmawiza Awang
Asmawiza Awang

Abstract
Uveal melanoma is a rare condition, especially in the Asian population that can be overlooked as a diagnostic consideration, leading to delayed identification. We reported the case of a 69-year-old Chinese man who presented with an iris mass that was initially treated as a cyst. The mass continued to grow in size, which raised suspicion of other infective causes or malignancy. Following the initial uveitic workup, the patient was found to be positive for QuantiFERON-TB test. Tumour markers and chest X-rays were unremarkable. The patient was treated for iris granuloma secondary to tuberculosis. However, the lesion continued to grow, prompting us to perform an excisional biopsy. Histopathological analysis demonstrated a mixed cellular (both spindle and epithelioid) pathology. The mixed cellular type has a higher metastatic potential compared to other histopathological types. This case highlighted the importance of ruling out malignant aetiology in cases of enlarging iris lesions to mitigate the risks of further complications.

Keywords : Excisional biopsy; iris melanoma; mixed cell melanoma,

Correspondance Address
Chiun Pei Rong. Department of Ophthalmology, Hospital Kuala Lumpur, Jalan Pahang, 50586 Kuala Lumpur, Malaysia / Department of Ophthalmology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Jalan Yaacob Latif, Bandar Tun Razak, 56000 Cheras, Kuala Lumpur, Malaysia. Tel: +603-2615 5555 ext 1462 Email: chiunpr88@gmail.com