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Updated: Jun 6, 2026

Endoscopic Endonasal Trans-sphenoidal Approach: Minimally Invasive Surgery for Pituitary Adenomas
Published on: January 17, 2018
Growth hormone-secreting adenoma with lack of retinoblastoma protein expression
Roberto Salvatori1,2, Gary L Gallia2,3, Calixto-Hope G Lucas2,4
1Division of Endocrinology Metabolism and Diabetes, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Abstract:
Retinoblastoma protein (Rb) is a tumor suppressor whose inactivation causes retinoblastomas, pineoblastomas, and possibly other central nervous system tumors. Although mice with Rb1 gene inactivation invariably develop pituitary adenomas, and some evidence suggests that a subset of pituitary adenomas have lack or reduced expression of Rb protein, to date no evidence has been reported that patients with germline mutations in the RB1 gene (that encodes for Rb protein) are at risk of developing pituitary adenomas. Here, we report the case of a patient with childhood (age 1 year) onset retinoblastoma because of a germline pathogenic variant of the RB1 gene who presented with a somatotropinoma diagnosed at a young age (20) and whose pituitary adenoma cells showed loss of expression of Rb protein by immunohistochemistry, suggesting a role of Rb in preventing the development of pituitary adenomas.
Insights
Germline RB1 gene mutations, linked to retinoblastoma, may also increase pituitary adenoma risk. A patient with retinoblastoma and a somatotropinoma showed loss of Rb protein expression, suggesting Rb
Area of Science:
- Oncology
- Genetics
- Endocrinology
Background:
- The Retinoblastoma (Rb) protein is a critical tumor suppressor involved in cell cycle regulation.
- Inactivation of the RB1 gene causes retinoblastomas and other central nervous system tumors.
- While mouse models show Rb inactivation leads to pituitary adenomas, human data linking germline RB1 mutations to pituitary adenomas is lacking.
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