Papillary Tumor of the Pineal Region in Children : Presentation of a Case and Comprehensive Literature Review

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Choque-Velasquez , J , Colasanti , R , Resendiz-Nieves , J , Jahromi , B R , Tynninen , O , Collan , J , Niemelä , M & Hernesniemi , J 2018 , ' Papillary Tumor of the Pineal Region in Children : Presentation of a Case and Comprehensive Literature Review ' , World Neurosurgery , vol. 117 , pp. 144-152 . https://doi.org/10.1016/j.wneu.2018.06.020

Title: Papillary Tumor of the Pineal Region in Children : Presentation of a Case and Comprehensive Literature Review
Author: Choque-Velasquez, Joham; Colasanti, Roberto; Resendiz-Nieves, Julio; Jahromi, Behnam Rezai; Tynninen, Olli; Collan, Juhani; Niemelä, Mika; Hernesniemi, Juha
Contributor organization: Clinicum
Neurokirurgian yksikkö
Department of Neurosciences
University of Helsinki
HUS Neurocenter
Department of Pathology
Medicum
HUSLAB
Department of Oncology
HUS Comprehensive Cancer Center
Date: 2018-09
Language: eng
Number of pages: 9
Belongs to series: World Neurosurgery
ISSN: 1878-8750
DOI: https://doi.org/10.1016/j.wneu.2018.06.020
URI: http://hdl.handle.net/10138/303784
Abstract: BACKGROUND: Papillary tumor of the pineal region (PTPR) is a rare grade II-III pineal lesion with peculiar histological and immunohistochemical features. These tumors mostly occur in adults, only rarely in children, with 19 cases reported up to now. CASE DESCRIPTION: We present a 3-year-old boy who underwent reoperation for a recurrent PTPR (grade II). Gross total resection of the lesion through an occipital interhemispheric approach with the patient in a sitting position was followed by adjuvant radiotherapy and chemotherapy. Histological examination revealed tumor progression (grade III) and an MIB-1 proliferation index >25%. The patient continues to do well with no evidence of recurrence more than 3 years following surgery. A comprehensive literature review regarding the PTPR, including the current management in children, is reported. CONCLUSIONS: PTPRs are extremely rare in children, and immunohistochemistry is needed to differentiate them from other pineal tumors. These tumors show a high rate of recurrence, and a multidisciplinary management approach (microsurgical resection followed by radiotherapy and/or chemotherapy) can help achieve a favorable outcome.
Subject: Children
Immunohistochemistry
Microneurosurgery
Multidisciplinary management
Papillary tumor of the pineal region
Pineal region lesions
Radiochemotherapy
OF-THE-LITERATURE
CENTRAL-NERVOUS-SYSTEM
SITTING POSITION
CLASSIFICATION
NEUROSURGERY
CHEMOTHERAPY
PROTOCOL
MULTICENTER
BEVACIZUMAB
PINEOCYTOMA
3112 Neurosciences
3124 Neurology and psychiatry
3126 Surgery, anesthesiology, intensive care, radiology
Peer reviewed: Yes
Rights: cc_by_nc_nd
Usage restriction: openAccess
Self-archived version: acceptedVersion


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