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What's new AAPOS 2008 - The Private Eye Clinic

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ANTERIOR SEGMENT<br />

Conjunctival Melanoma 3 Years after Radiation and Chemotherapy for<br />

Retinoblastoma.<br />

JPOS 2007; 44:300-302.<br />

An 8-month old infant with advanced bilateral retinoblastoma was managed with<br />

enucleation of the right eye and chemotherapy and radiotherapy of the left eye. Three<br />

years after treatment, excisional biopsy of a non-pigmented mass in the anopthalmic<br />

right socket demonstrated amelanotic melanoma of the conjunctiva with superficial<br />

orbital invasion. No tumor recurrence has been noted in 20 months of follow-up.<br />

Potential causes of this unusual occurrence are discussed including germline mutation<br />

and the importance of systemic monitoring in patients with retinoblastoma.<br />

Malignant Melanoma of the Conjunctiva in Children: An Review of the<br />

International Literature 1965-2006.<br />

JPOS 2007; 44:277-282.<br />

Malignant melanoma of the conjunctiva is an uncommon but potentially life-threatening<br />

ocular tumor which primarily affects white adults between the fourth and seventh<br />

decades of life. Conjuctival melanoma is rare in children. A review of the literature<br />

resulted in 28 reported cases in children younger than 15 years and only 8 had<br />

adequate details noted. Conjunctival melanoma is approx-imately 18-40 times less<br />

frequent than uveal melanoma. Conjunctival melanomas can evolve from melanocytic<br />

nevi or primary aquired melanosis or they can arise de novo. Due to the rarity of<br />

conjunctival melanoma in children, other more common diagnoses should be<br />

considered in the work-up. . <strong>The</strong> small numbers provided in this review prevent<br />

drawing conclusions with any confidence.<br />

41

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