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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