Literature DB >> 27239462

Late Presentation of Retinoblastoma in a Teen with Aicardi Syndrome.

Patricia Y Akinfenwa1, Patricia Chévez-Barrios2, Clio A Harper3, Dan S Gombos4.   

Abstract

BACKGROUND/AIMS: Retinoblastoma (Rb) generally presents in children <8 years of age. Aicardi syndrome (AS) is a congenital, neurodevelopmental disorder that has been associated with various ophthalmic abnormalities, but no reports have related it to a delayed presentation of Rb. This report describes the late presentation of Rb in a teenage patient with AS and suggests modifications in ophthalmic screening to facilitate early detection.
METHODS: A chart review was conducted of a patient with AS. We examined the ophthalmic history, fundus images and B-scan ultrasonography. Histopathological analysis was conducted on globe sections.
RESULTS: The patient's ophthalmic history was consistent with normal findings of AS: fundus images and B-scan ultrasonography revealed chorioretinal lacunae and an area of retinal detachment, respectively. The patient presented with chronic irritation and mydriasis of the blind left eye. This was enucleated as treatment. Histopathology revealed a focally differentiated Rb. Immunohistochemistry demonstrated that the tumor cells were positive for synaptophysin and negative for the wild-type Rb protein, and a high Ki-67 proliferation index was shown.
CONCLUSION: Our patient was diagnosed with Rb at age 16. AS has been associated with numerous ophthalmic findings, but this is the first report relating it to a late Rb presentation. Meticulous ophthalmic examinations should be considered through the teenage years and early adulthood of AS patients.

Entities:  

Keywords:  Aicardi syndrome; Ocular pathology; Ocular tumors; Retinoblastoma

Year:  2016        PMID: 27239462      PMCID: PMC4881269          DOI: 10.1159/000439595

Source DB:  PubMed          Journal:  Ocul Oncol Pathol        ISSN: 2296-4657


  9 in total

1.  Ophthalmologic findings in Aicardi syndrome.

Authors:  Gary Fruhman; Tanya N Eble; Nikki Gambhir; V Reid Sutton; Ignatia B Van den Veyver; Richard A Lewis
Journal:  J AAPOS       Date:  2012-06       Impact factor: 1.220

2.  Bilateral retinoblastoma in a male patient with an X; 13 translocation: evidence for silencing of the RB1 gene by the spreading of X inactivation.

Authors:  C Jones; C Booth; D Rita; L Jazmines; B Brandt; A Newlan; B Horsthemke
Journal:  Am J Hum Genet       Date:  1997-06       Impact factor: 11.025

3.  Retinoblastoma in an eye with congenital uveal coloboma.

Authors:  M D Mills; N Syed
Journal:  J AAPOS       Date:  1998-10       Impact factor: 1.220

Review 4.  Classification of microphthalmos and coloboma.

Authors:  M Warburg
Journal:  J Med Genet       Date:  1993-08       Impact factor: 6.318

5.  Possible inactivation of part of chromosome 13 due to 13qXp translocation associated with retinoblastoma.

Authors:  Y Ejima; M S Sasaki; A Kaneko; H Tanooka; Y Hara; T Hida; Y Kinoshita
Journal:  Clin Genet       Date:  1982-06       Impact factor: 4.438

6.  Further observations on a 13qXp translocation associated with retinoblastoma.

Authors:  W W Nichols; R C Miller; M Sobel; E Hoffman; R S Sparkes; T Mohandas; I Veomett; J R Davis
Journal:  Am J Ophthalmol       Date:  1980-05       Impact factor: 5.258

7.  The genetics of retinoblastoma, revisited.

Authors:  A Naumova; C Sapienza
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

8.  Interstitial deletion of 13q and a 13;X chromosome translocation results in partial trisomy 13 and bilateral retinoblastoma.

Authors:  David Dries; Katrina Baca; Lisa Truss; Sheila Dobin
Journal:  Ophthalmic Genet       Date:  2003-09       Impact factor: 1.803

Review 9.  Aicardi syndrome.

Authors:  Tena Rosser
Journal:  Arch Neurol       Date:  2003-10
  9 in total

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