ABSTRACT
Retinoblastoma (RB) is the most common primary malignant intraocular tumor of childhood presenting usually before 5 years of age. RB in adults older than 20 years is extremely rare. A literature search using PubMed/PubMed Central, Scopus, Google Scholar, EMBASE, and Cochrane databases revealed only 45 cases till date. Over the past decade, there has been a significant increase in the number of such reports, indicating heightened level of suspicion among ophthalmologists. Compared to its pediatric counterpart, adult onset RB poses unique challenges in diagnosis and treatment. This article summarizes available literature on adult onset RB and its clinical and pathologic profile, genetics, association with retinocytoma, diagnostics, treatment, and outcomes.
ABSTRACT
Retinocytoma is a benign tumor arising from the retina.Since it was first described by Gallie in 1982,retinocytoma has been progressively recognized.More and more clinical and pathological studies indicate that retinocytoma may be a early stage or a type of retinoblastoma.Retinocytoma is difficult to be found because of lack clinical signs.Therefore,it is very important for us to follow-up and screen the families of RB patient in order to intervene with the course of disease as early as possible for preventing and arresting the malignization of retinocytoma toward RB.The name alteration,clinical manifestations,histopathological features,molecular mechanism and heredity characteristics were reviewed.
ABSTRACT
A 3-year-old girl presented with left exotropia. Funduscopy demonstrated a retinocytoma associated with five discrete retinoblastomas in the left eye and three discrete retinoblastomas in her right eye. The clinical manifestations and fundus imaging findings are described.