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Trilateral retinoblastoma.

C Stolovitch1, A Loewenstein, D Varssano

  • 1Department of Ophthalmology, Ichilov Hospital, Tel Aviv, Israel.

Metabolic, Pediatric, and Systemic Ophthalmology (New York, N.Y. : 1985)
|January 1, 1992
PubMed
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Retinoblastoma, a childhood eye cancer, can present as trilateral retinoblastoma. This rare syndrome involves bilateral retinoblastoma and a brain tumor, as seen in a pediatric case study.

Area of Science:

  • Pediatric Oncology
  • Ophthalmology
  • Neuro-oncology

Background:

  • Retinoblastoma is the most frequent intraocular cancer in children.
  • Trilateral retinoblastoma is a specific syndrome defined by bilateral retinoblastoma and an intracranial neuroblastic tumor.

Observation:

  • A case of a three-year-old girl with trilateral retinoblastoma is presented.
  • The intracranial tumor was located in the pineal, suprasellar, or parasellar region.

Findings:

  • The study details a rare presentation of trilateral retinoblastoma in a young child.
  • A review of existing literature on this syndrome is included.

Implications:

  • Highlights the importance of recognizing trilateral retinoblastoma for timely diagnosis and treatment.

Related Experiment Videos

  • Emphasizes the need for comprehensive evaluation in cases of bilateral retinoblastoma.
  • Contributes to the understanding of this rare pediatric cancer syndrome.