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2019, Number 4

Rev Fac Med UNAM 2019; 62 (4)

Retinoblastoma: a frequent eye tumor in childhood

Pérez HMA, Domínguez CPM
Full text How to cite this article

Language: Spanish
References: 11
Page: 35-38
PDF size: 160.95 Kb.


Key words:

Retinoblastoma, eye neoplasms, pediatrics, eye enucleation.

ABSTRACT

Retinoblastoma is one of the most frequent malignant intraocular tumors in the pediatric age group, and it is possible that there is affectation to other sites such as the contralateral eye, hence, it is important to maintain periodic controls even after being diagnosed and treated.
Currently it is known that this pathology can be either hereditary or spontaneous and has an important genetic component, specifically a mutation of the tumor-suppressor gene called RB1, which is also associated with other diseases.


REFERENCES

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  3. Rodriguez-Galindo COD. Retinoblastoma. Pediatric Clinics of Norht America. 2015;62(1):201-23.

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  8. Villamil Duarte JF, Quintero Pérez LM. Clinical, diagnostic and therapeutic considerations in retinoblastoma. MedUNAB. 2011;14(3):180-7.

  9. Rodjan F, De Graaf P, Van der Valk P, Hadjistilianou T, Cerase A, Toti P, et al. Detection of Calcifications in Retinoblastoma Using Gradient- Echo MRImaging Sequences: Comparative Study between In Vivo MRImaging and Ex Vivo High-Resolution CT. AJNR Am J Neuroradiol. 2015;36:355-60.

  10. Mazurowski MA. Radiogenomics: What It Is and Why It Is Important. J Am Coll Radiol. 2015;12(8):862-6.

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Rev Fac Med UNAM . 2019;62