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PEDT-07 RECURRENT MEDULLOBLASTOMA 9 YEARS AFTER THE PRIMARY TUMOR

Medulloblastoma is one of the most common malignant brain tumors in children. Despite multi-disciplinary treatment for medulloblastoma, including surgery, chemotherapy, and radiation, which have resulted in significant improvement of the prognosis, about 30% of patients still experience recurrence....

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Autores principales: Hiraki, Takamasa, Fukuoka, Kouhei, Tsumura, Yusuke, Inoue, Kyohei, Tomita, Osamu, Mitani, Yuichi, Ohshima, Kouichi, Mori, Makiko, Arakawa, Yuki, Tanami, Yutaka, Nakazawa, Atsuko, Kurihara, Jun, Koh, Katsuyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213110/
http://dx.doi.org/10.1093/noajnl/vdz039.075
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author Hiraki, Takamasa
Fukuoka, Kouhei
Tsumura, Yusuke
Inoue, Kyohei
Tomita, Osamu
Mitani, Yuichi
Ohshima, Kouichi
Mori, Makiko
Arakawa, Yuki
Tanami, Yutaka
Nakazawa, Atsuko
Kurihara, Jun
Koh, Katsuyoshi
author_facet Hiraki, Takamasa
Fukuoka, Kouhei
Tsumura, Yusuke
Inoue, Kyohei
Tomita, Osamu
Mitani, Yuichi
Ohshima, Kouichi
Mori, Makiko
Arakawa, Yuki
Tanami, Yutaka
Nakazawa, Atsuko
Kurihara, Jun
Koh, Katsuyoshi
author_sort Hiraki, Takamasa
collection PubMed
description Medulloblastoma is one of the most common malignant brain tumors in children. Despite multi-disciplinary treatment for medulloblastoma, including surgery, chemotherapy, and radiation, which have resulted in significant improvement of the prognosis, about 30% of patients still experience recurrence. Most recurrences occur within the first 15 months from diagnosis and late relapse of the tumor is quite rare. We report a case of a 15-year-old female patient with recurrent medulloblastoma 9 years after the primary tumor. At the age of 6, this patient developed a posterior fossa tumor without metastasis and underwent near-total resection. The pathological diagnosis was medulloblastoma with focal desmoplasia. After the surgery, she received multi-agent chemotherapy and radiation therapy consisting of 18 Gy craniospinal irradiation and 51.2 Gy local irradiation. She was in complete remission for 9 years after the treatment. However, gait disturbance began to gradually appear, and magnetic resonance imaging (MRI) showed an intradural lesion in her thoracic spine. The lesion was biopsied, and the pathological findings confirmed the recurrence of medulloblastoma. Currently, we plan to administer local radiation therapy concomitantly with temozolomide to the patient. The case reminds us of the importance of long-term careful follow-up of patients with medulloblastoma. Further studies are warranted for the treatment of relapsed medulloblastomas due to the limited information available at present.
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spelling pubmed-72131102020-07-07 PEDT-07 RECURRENT MEDULLOBLASTOMA 9 YEARS AFTER THE PRIMARY TUMOR Hiraki, Takamasa Fukuoka, Kouhei Tsumura, Yusuke Inoue, Kyohei Tomita, Osamu Mitani, Yuichi Ohshima, Kouichi Mori, Makiko Arakawa, Yuki Tanami, Yutaka Nakazawa, Atsuko Kurihara, Jun Koh, Katsuyoshi Neurooncol Adv Abstracts Medulloblastoma is one of the most common malignant brain tumors in children. Despite multi-disciplinary treatment for medulloblastoma, including surgery, chemotherapy, and radiation, which have resulted in significant improvement of the prognosis, about 30% of patients still experience recurrence. Most recurrences occur within the first 15 months from diagnosis and late relapse of the tumor is quite rare. We report a case of a 15-year-old female patient with recurrent medulloblastoma 9 years after the primary tumor. At the age of 6, this patient developed a posterior fossa tumor without metastasis and underwent near-total resection. The pathological diagnosis was medulloblastoma with focal desmoplasia. After the surgery, she received multi-agent chemotherapy and radiation therapy consisting of 18 Gy craniospinal irradiation and 51.2 Gy local irradiation. She was in complete remission for 9 years after the treatment. However, gait disturbance began to gradually appear, and magnetic resonance imaging (MRI) showed an intradural lesion in her thoracic spine. The lesion was biopsied, and the pathological findings confirmed the recurrence of medulloblastoma. Currently, we plan to administer local radiation therapy concomitantly with temozolomide to the patient. The case reminds us of the importance of long-term careful follow-up of patients with medulloblastoma. Further studies are warranted for the treatment of relapsed medulloblastomas due to the limited information available at present. Oxford University Press 2019-12-16 /pmc/articles/PMC7213110/ http://dx.doi.org/10.1093/noajnl/vdz039.075 Text en © The Author(s) 2019. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Hiraki, Takamasa
Fukuoka, Kouhei
Tsumura, Yusuke
Inoue, Kyohei
Tomita, Osamu
Mitani, Yuichi
Ohshima, Kouichi
Mori, Makiko
Arakawa, Yuki
Tanami, Yutaka
Nakazawa, Atsuko
Kurihara, Jun
Koh, Katsuyoshi
PEDT-07 RECURRENT MEDULLOBLASTOMA 9 YEARS AFTER THE PRIMARY TUMOR
title PEDT-07 RECURRENT MEDULLOBLASTOMA 9 YEARS AFTER THE PRIMARY TUMOR
title_full PEDT-07 RECURRENT MEDULLOBLASTOMA 9 YEARS AFTER THE PRIMARY TUMOR
title_fullStr PEDT-07 RECURRENT MEDULLOBLASTOMA 9 YEARS AFTER THE PRIMARY TUMOR
title_full_unstemmed PEDT-07 RECURRENT MEDULLOBLASTOMA 9 YEARS AFTER THE PRIMARY TUMOR
title_short PEDT-07 RECURRENT MEDULLOBLASTOMA 9 YEARS AFTER THE PRIMARY TUMOR
title_sort pedt-07 recurrent medulloblastoma 9 years after the primary tumor
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213110/
http://dx.doi.org/10.1093/noajnl/vdz039.075
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