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Pineal Region Tumors in Children Homepage

This page was last updated on June 9th, 2022

Authors

Amanda Muhs Saratsis, M.D.
Tadanori Tomita, M.D.

Section Editor

Kristian Aquilina, M.D.

Editor in Chief

Rick Abbott, M.D.

Introduction

The pineal gland is a neuroendocrine organ located in the posterior aspect of the third ventricle in close proximity to a variety of important neurovascular structures.  The gland is composed of pineocytes, a specialized population of neuronal cells, and supporting glial cells.  As a result of this varied histology and dense regional anatomy, tumors of the pineal region are heterogeneous in nature with variable natural history and treatment paradigms, dependent on the cell of origin.

Key Points

  • Pineal gland cells give rise to a variety of tumors: The variety of tumors arising in the pineal region reflects the complex histology and dense anatomy of the area.
  • Variation in biology with tumor type: The natural history, treatment, and prognosis of pineal region tumors depend on tumor type.
  • Improved management with improved tools: Advances in neuroimaging, immunohistochemical techniques, and tumor marker testing have improved diagnosis and management of pineal region tumors. The refinement of surgical approaches to the pineal region, coupled with the availability of the surgical microscope and neuroendoscopy, has made resection of pineal region tumors a viable treatment modality.
  • Adjuvant therapies important: Chemotherapy and radiation therapy remain important tools in the management of pineal region tumors.

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