Retinoblastoma as a possible primary intracranial tumor

E. Bullitt; B. J. Crain

doi:10.1227/00006123-198112000-00016

Retinoblastoma as a possible primary intracranial tumor

E. Bullitt, B. J. Crain

Research output: Contribution to journal › Article › peer-review

18 Scopus citations

Abstract

A 10-month-old infant with a small, unilateral, peripheral retinal lesion also had a large, well-encapsulated, suprasellar retinoblastoma. The primary vs. the metastatic nature of the intracranial tumor is considered. It is postulated that primary intracranial tumors may arise within areas of the central nervous system embryologically related to the retina in patients with the genetic form of retinoblastoma.

Original language	English (US)
Pages (from-to)	706-709
Number of pages	4
Journal	Neurosurgery
Volume	9
Issue number	6
DOIs	https://doi.org/10.1227/00006123-198112000-00016
State	Published - Jan 1 1981
Externally published	Yes

ASJC Scopus subject areas

Surgery
Clinical Neurology

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10.1227/00006123-198112000-00016

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abstract = "A 10-month-old infant with a small, unilateral, peripheral retinal lesion also had a large, well-encapsulated, suprasellar retinoblastoma. The primary vs. the metastatic nature of the intracranial tumor is considered. It is postulated that primary intracranial tumors may arise within areas of the central nervous system embryologically related to the retina in patients with the genetic form of retinoblastoma.",

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AB - A 10-month-old infant with a small, unilateral, peripheral retinal lesion also had a large, well-encapsulated, suprasellar retinoblastoma. The primary vs. the metastatic nature of the intracranial tumor is considered. It is postulated that primary intracranial tumors may arise within areas of the central nervous system embryologically related to the retina in patients with the genetic form of retinoblastoma.

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Retinoblastoma as a possible primary intracranial tumor

Abstract

ASJC Scopus subject areas

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