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CS-14 A CASE OF CIC-REARRANGED INTRACRANIAL SARCOMA

INTRODUCTION: Intracranial sarcoma is extremely rare among primary brain tumors and often misdiagnosed. Its standard treatment is yet to be established, and treatment options are discussed on a case-by-case basis. Here we report our recent case of intracranial sarcoma review the relevant literature....

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Autores principales: Tanaka, Shota, Sato, Daisuke, Ikemura, Masako, Takayanagi, Shunsaku, Tsutsumi, Kazuo, Saito, Nobuhito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213107/
http://dx.doi.org/10.1093/noajnl/vdz039.183
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author Tanaka, Shota
Sato, Daisuke
Ikemura, Masako
Takayanagi, Shunsaku
Tsutsumi, Kazuo
Saito, Nobuhito
author_facet Tanaka, Shota
Sato, Daisuke
Ikemura, Masako
Takayanagi, Shunsaku
Tsutsumi, Kazuo
Saito, Nobuhito
author_sort Tanaka, Shota
collection PubMed
description INTRODUCTION: Intracranial sarcoma is extremely rare among primary brain tumors and often misdiagnosed. Its standard treatment is yet to be established, and treatment options are discussed on a case-by-case basis. Here we report our recent case of intracranial sarcoma review the relevant literature. CASE ILLUSTRATION: A 57-year-old right-handed man presented with headache and was found to have a 5cm mass in the right frontal lobe. Gross total resection was achieved without complications. Given the local pathological diagnosis being glioblastoma, adjuvant radiotherapy with concurrent temozolomide was administered. Further pathological examination revealed Capicua (CIC) rearrangement on FISH, which lead to the diagnosis of sarcoma. No further treatment was pursued at that time. However, he noticed rapid decline in the right visual acuity 7 months from the initial diagnosis. MRI demonstrated a rapidly-growing mass in the right optic nerve sized 1.5cm, which was depicted as a high uptake area on FDG-PET, suggestive of recurrence. Two cycles of chemotherapy with vincristine, ifosfamide, doxorubicin, and etoposide as well as GammaKnife stereotactic radiosurgery were performed with partial response. Sustained myelosuppression and debilitating constitutional symptoms precluded additional chemotherapy. No further recurrence was noted 1 year after diagnosis. CONCLUSION: We have recently experienced a case of CIC-rearranged intracranial sarcoma. FISH was useful in detecting CIC rearrangement and reaching the correct pathological diagnosis. Rapid recurrence of the tumor was noted, but well controlled with radiochemotherapy.
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spelling pubmed-72131072020-07-07 CS-14 A CASE OF CIC-REARRANGED INTRACRANIAL SARCOMA Tanaka, Shota Sato, Daisuke Ikemura, Masako Takayanagi, Shunsaku Tsutsumi, Kazuo Saito, Nobuhito Neurooncol Adv Abstracts INTRODUCTION: Intracranial sarcoma is extremely rare among primary brain tumors and often misdiagnosed. Its standard treatment is yet to be established, and treatment options are discussed on a case-by-case basis. Here we report our recent case of intracranial sarcoma review the relevant literature. CASE ILLUSTRATION: A 57-year-old right-handed man presented with headache and was found to have a 5cm mass in the right frontal lobe. Gross total resection was achieved without complications. Given the local pathological diagnosis being glioblastoma, adjuvant radiotherapy with concurrent temozolomide was administered. Further pathological examination revealed Capicua (CIC) rearrangement on FISH, which lead to the diagnosis of sarcoma. No further treatment was pursued at that time. However, he noticed rapid decline in the right visual acuity 7 months from the initial diagnosis. MRI demonstrated a rapidly-growing mass in the right optic nerve sized 1.5cm, which was depicted as a high uptake area on FDG-PET, suggestive of recurrence. Two cycles of chemotherapy with vincristine, ifosfamide, doxorubicin, and etoposide as well as GammaKnife stereotactic radiosurgery were performed with partial response. Sustained myelosuppression and debilitating constitutional symptoms precluded additional chemotherapy. No further recurrence was noted 1 year after diagnosis. CONCLUSION: We have recently experienced a case of CIC-rearranged intracranial sarcoma. FISH was useful in detecting CIC rearrangement and reaching the correct pathological diagnosis. Rapid recurrence of the tumor was noted, but well controlled with radiochemotherapy. Oxford University Press 2019-12-16 /pmc/articles/PMC7213107/ http://dx.doi.org/10.1093/noajnl/vdz039.183 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
Tanaka, Shota
Sato, Daisuke
Ikemura, Masako
Takayanagi, Shunsaku
Tsutsumi, Kazuo
Saito, Nobuhito
CS-14 A CASE OF CIC-REARRANGED INTRACRANIAL SARCOMA
title CS-14 A CASE OF CIC-REARRANGED INTRACRANIAL SARCOMA
title_full CS-14 A CASE OF CIC-REARRANGED INTRACRANIAL SARCOMA
title_fullStr CS-14 A CASE OF CIC-REARRANGED INTRACRANIAL SARCOMA
title_full_unstemmed CS-14 A CASE OF CIC-REARRANGED INTRACRANIAL SARCOMA
title_short CS-14 A CASE OF CIC-REARRANGED INTRACRANIAL SARCOMA
title_sort cs-14 a case of cic-rearranged intracranial sarcoma
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7213107/
http://dx.doi.org/10.1093/noajnl/vdz039.183
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