intraocular neoplasm originating from immature retinal cells (retinoblasts) in retinal development. Case Report 6 month before 4 month before admission admission admission • the right eye • the right eye • bump in his started to started to right eye protrude protrude • bump in his and got and got right eye bigger as a bigger as a Right Eye Left Eye • a white dot ping pong ping pong appeared in ball and ball and the middle bleeds easily bleeds easily of the eye • Lymphadeno • Lymphadeno • Painful pathy pathy multiple multiple • Blind • blind • Weight lost Discussion
The pathogenesis of retinoblastoma is caused by mutations in the RB1 gene
located on chromosome 13q14. This disease can be heritable or non- heritable. The most common clinical presentation of retinoblastoma is leukocoria followed by strabismus. leukocoria seen in 22.6% to 97.9% of retinoblastoma patients, whereas 5.6% to 26% of patients showed symptoms of strabismus. To establish a definite diagnosis of retinoblastoma, it is necessary to carry out additional investigations. Based on the literature, imaging modalities that can be used include ultrasonography, CT-scan, MRI and biopsy. The preferred therapeutic management is multimodal therapy with a combination of high-dose initial chemotherapy, surgery (orbital enucleation/exenteration), radiotherapy and continued chemotherapy as much as 12 cycles. Conclusion
Retinoblastoma should be considered as an intraocular tumors especially in
children until proven otherwise. Specifically in areas with limited facilities, it is very important to be able to detect early signs of retinoblastoma and avoid development of disease to worse stage (extraocular retinoblastoma). In particular, in areas with limited health facilities, it is very important to increase the awareness of the general public and health workers in recognizing early signs and symptoms of retinoblastoma, in addition it is also necessary to provide equitable health facilities to establish the diagnosis and treatment of this disease.
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