Bilateral Retinoblastoma Presenting in an in vitro Fertilization Infant with Retinopathy of Prematurity

Ruba Saleh Alghofaili1,2, Saleh A Almesfer2

  • 1Department of Ophthalmology, College of Medicine, Qassim University, Qassim, Saudi Arabia.

Insights

Retinopathy of prematurity (ROP) and retinoblastoma (RB) can co-occur in infants. This case report details an infant conceived via IVF who developed RB after ROP treatment, underscoring the need for ongoing eye surveillance.

Area of Science:

  • Ophthalmology
  • Neonatology
  • Genetics

Background:

  • Retinopathy of prematurity (ROP) is a developmental disorder affecting premature infants.
  • Retinoblastoma (RB) is a genetic malignancy of the retina.
  • Co-occurrence of ROP and RB is rare but reported.

Observation:

  • An infant conceived via in vitro fertilization (IVF) presented with advanced-stage ROP.
  • Following ROP treatment, the infant developed bilateral retinoblastoma.
  • The RB necessitated bilateral enucleation despite initial ROP management.

Findings:

  • This is the sixth reported case of co-occurring ROP and RB.
  • The infant's history includes IVF conception and advanced ROP.
  • The temporal association raises questions about potential links between IVF, ROP, and RB.

Implications:

  • While causal links are unlikely, the case highlights the importance of vigilant follow-up for ROP patients.
  • Early detection and management of ocular sequelae, including retinoblastoma, are crucial.
  • Further research may explore potential shared risk factors or biological interactions.