Rubeose irienne revealing a retinoblastome: a case report

Research Area: Medicine
Authors
Salma HASSINA* Ihssane HASNAOUI Mohamed Amine KRICHENE Chaimaa BARDI Loubna ROBBANA N TEBBAY B BEKKAR Youness AKKANOUR Louay SERGHINI El Hassan ABDALAH
Ophthalmology B, Ibn-Sina University Hospital RABAT MOROCCO

Abstract
Retinoblastoma, the most common malignant ocular tumor in infancy, primarily affects children under five, with peak onset at one year for hereditary bilateral cases and two years for sporadic unilateral cases. Rarely, it affects older children and adults, complicating diagnosis.

Keywords
Retinoblastoma; Malignant ocular tumor; Childhood eye cancer; Strabismus; Unilateral retinoblastoma; Endophytic retinoblastoma;

Doi : https://doi.org/10.5281/zenodo.12594569

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Cite
HASSINA, S., HASNAOUI, I., KRICHENE, M. A., BARDI, C., ROBBANA, L., TEBBAY, N., BEKKAR, B., AKKANOUR, Y., SERGHINI, L., & ABDALAH, E. H. (2024). Rubeose irienne revealing a retinoblastome: a case report. International Journal of Science, Applications and Prosperity, 2(1), 53‑59.

Licence
cc-by-4.0 icon Copyright @ by the authors. This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).

References
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[4] Schaiquevich P, Francis JH, Cancela MB, Carcaboso AM, Chantada GL, Abramson DH. Treatment of Retinoblastoma: What Is the Latest and What Is the Future. Front Oncol. 2022 Apr 1;12:822330. doi: 10.3389/fonc.2022.822330. PMID: 35433448; PMCID: PMC9010858.
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