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dc.contributor.authorAtwine, Raymond
dc.contributor.authorLaffita, Damaris
dc.contributor.authorBirungi, Abraham
dc.contributor.authorKiconco, Ritah
dc.contributor.authorWaddell, Keith
dc.date.accessioned2024-01-31T12:29:42Z
dc.date.available2024-01-31T12:29:42Z
dc.date.issued2023
dc.identifier.citationAtwine, R., Laffita, D., Birungi, A., Kiconco, R., & Waddell, K. (2023). Clinical and Histopathologic Predictors of Survival Among Children With Retinoblastoma From Two Tertiary Health Facilities in Uganda. Cureus, 15(12).en_US
dc.identifier.urihttp://ir.must.ac.ug/xmlui/handle/123456789/3363
dc.description.abstractBackground: Retinoblastoma (RB) is a malignant tumour that develops from the immature cells of the retina. It is the most frequent type of paediatric intraocular cancer and is curable. Clinical and histological findings after enucleation of the affected eye dictate not only the patient's secondary care but also their prognosis. We assessed the clinical and histopathologic predictors of survival among children with RB from two tertiary health facilities in Uganda. Methods: This retrospective research utilized archived formalin fixed and paraffin-embedded blocks of eye specimens enucleated between 2014 and 2016 at Mbarara University of Science and Technology (MUST) Pathology Department and Ruharo Eye Centre (REC) in Mbarara, Uganda. The specimens were then processed and stained with haematoxylin and eosin. The confirmation of RB was made to include the histologic stage and features of the tumor. Biographic data of the patients and clinical features, such as leukocoria, proptosis, phthisis, staphyloma and buphthalmos, were retrieved from the records. Results: Males (55.1%, n=43) dominated the study population (N=78). The median age was 31 months. The most common clinical sign was leukocoria (69.2%, n=52), and the most predominant histopathological stage was stage 1 (41%, n=32). Optic nerve (ON) invasion was seen in 38.5% (n=30), choroidal invasion in 29.5% (n=23), scleral invasion in 7.7% (n=6) and orbital extension in 16.7% (n=13) of the cases. FlexnerWintersteiner rosettes were seen in 34.6% (n=27). Necrosis was a prominent feature (71.8%, n=56). The twoyear survival was estimated to be 61.5% (n=48). Leukocoria (risk ratio (RR) 1.1), female gender (RR 1.4), intralaminar ON invasion (RR 7.6) and a lack of orbital extension (RR 7) were significant predictors of survival. Conclusion: Leukocoria and proptosis are noticeable clinical signs of RB. Most patients present while in stage one although stage four presentation is also common. Leukocoria, ON invasion, orbital extension and gender are significant factors predictive of survival in patients with RBen_US
dc.language.isoen_USen_US
dc.publisherCureusen_US
dc.subjectChildrenen_US
dc.subjectSurvivalen_US
dc.subjectRetinoblastomaen_US
dc.subjectFeaturesen_US
dc.subjectPathologicalen_US
dc.subjectHistologyen_US
dc.subjectClinical featuresen_US
dc.subjectPredictorsen_US
dc.subjectUgandaen_US
dc.titleClinical and Histopathologic Predictors of Survival Among Children With Retinoblastoma From Two Tertiary Health Facilities in Ugandaen_US
dc.typeArticleen_US


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