Clinical experience and outcomes in patients with pineal parenchymal tumor of intermediate differentiation (PPTID): a single-institution analysis.

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Abstract

Pineal parenchymal tumor of intermediate differentiation (PPTID) is a neoplasm of pinealocyte origin and of intermediate differentiation (WHO grade 2 or 3). Treatment selection and prognostication is challenging for this rare, recently characterized tumor. In this single study, we review our clinical experience in patients with PPTID as well as pooled data from two other institutions.

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Author and article information

Journal

Journal ID (iso-abbrev): J Neurooncol

Title: Journal of neuro-oncology

Publisher: Springer Science and Business Media LLC

ISSN (Electronic): 1573-7373

ISSN (Print): 0167-594X

Publication date (Electronic): Nov 2022

Volume: 160

Issue: 2

Affiliations

[1 ] Department of Hematology/Oncology, Mayo Clinic, Rochester, MN, USA. webb.mason@mayo.edu.

[2 ] Department of Radiology, Mayo Clinic, Rochester, MN, USA.

[3 ] Department of Neurology, Mayo Clinic, Rochester, MN, USA.

[4 ] Department of Radiation Oncology, Mayo Clinic, Rochester, MN, USA.

[5 ] Department of Oncology, Mayo Clinic, Rochester, MN, USA.

Article

Publisher Item ID: 10.1007/s11060-022-04174-6

DOI: 10.1007/s11060-022-04174-6

PubMed ID: 36301435

SO-VID: 3977e47b-b11d-4bac-a177-6d5c69892056

History

Keywords: Pineal,Radiation therapy,Outcome,Parenchymal tumor of intermediate differentiation (PPTID),Primary CNS tumors

Data availability:

Keywords: Pineal, Radiation therapy, Outcome, Parenchymal tumor of intermediate differentiation (PPTID), Primary CNS tumors

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