Patient with Refractory Epilepsy Associated with Oligondendroglioma

Mauricio Vaillant Amarante; Ozinelia Pedroni Batista; Camilia Lampier Lutzke; Shirley Kempin Quiqui

doi:doi:10.11648/j.cnn.20190302.13

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Patient with Refractory Epilepsy Associated with Oligondendroglioma

Mauricio Vaillant Amarante, Ozinelia Pedroni Batista, Camilia Lampier Lutzke, Shirley Kempin Quiqui

Published in Clinical Neurology and Neuroscience (Volume 3, Issue 2)

Received: 23 April 2019 Accepted: 5 June 2019 Published: 20 June 2019

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Abstract

Oligodendroglioma is a rare form of primary brain tumor, accounting for about 2-5% of intracranial tumors, being more common in adult males but rare in children, accounting for about 1-2% of all primary brain tumors in children. It originates from oligodendrocytes or glial precursor cells and exhibits infiltrative and slow growth. They can be classified in two grades (Grade II and Grade III), where Grade II are low grade tumors and have tumor cells that grow slowly and invade nearby normal tissue, and Grade III are malignant and have rapidly growing tumors. It has low growth and 50-80% of cases first symptom is seizures. A seizure is a symptom that requires a rapid solution usually requiring empirical treatment at the initial time to cease seizures and promote some well-being for the patient's routine. Seizures can cause a lot of damage to the patient's life, especially if the patient is a child who does not know what to do and what to do. Depending on the intensity and frequency of seizure episodes, the patient may experience fractures with falls, may suffer discrimination and prejudice at school. The causes behind refractory epilepsy are diverse, so whenever a patient is found to be refractory to drug treatment, the origin of seizures should be investigated early, it is not enough to stop at empirical treatment.

Published in	Clinical Neurology and Neuroscience (Volume 3, Issue 2)
DOI	10.11648/j.cnn.20190302.13
Page(s)	43-45
Creative Commons	This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.
Copyright	Copyright © The Author(s), 2019. Published by Science Publishing Group

Keywords

Olingodendroglioma, Refractory Epilepsy, Primary Brain Tumors

References

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[3]	Ducray F, Idbaih A, de Reyniès A, et al. (2008). "Anaplastic oligodendrogliomas with 1p19q codeletion have a proneural gene expression profile". Mol. Cancer. 7: 41. doi: 10.1186/1476-4598-7-41. PMC 2415112. PMID 18492260.
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[6]	Lassman, A. B. (20 May 2009). "Retrospective analysis of outcomes among more than 1,000 patients with newly diagnosed anaplastic oligodendroglial tumors". Journal of Clinical Oncology. 27 (15S): 2014. doi: 10.1200/jco.2009.27.15s.2014 (inactive 2019-02-12). ISSN 0732-183X.
[7]	Sunyach MP, Jouvet A, Perol D, et al. (December 2007). "Role of exclusive chemotherapy as first line treatment in oligodendroglioma". J. Neurooncol. 85 (3): 319–28. doi: 10.1007/s11060-007-9422-3. PMID 17568995.
[8]	Ohgaki H, Kleihues P (June 2005). "Population-based studies on incidence, survival rates, and genetic alterations in astrocytic and oligodendroglial gliomas". J Neuropathol Exp Neurol. 64 (6): 479–489. doi:10.1093/jnen/64.6.479. PMID 15977639.
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[11]	Huang CI, Chiou WH, Ho DM (December 1987). "Oligodendroglioma occurring after radiation therapy for pituitary adenoma". Journal of Neurology, Neurosurgery & Psychiatry. 50 (12): 1619–24. doi: 10.1136/jnnp.50.12.1619. PMC 1032603. PMID 3325615.
[12]	Laigle-Donadey F, Benouaich-Amiel A, Hoang-Xuan K, Sanson M (2005). "[Molecular biology of oligodendroglial tumors]". Neuro-Chirurgie (in French). 51 (3–4 Pt 2): 260–8. doi: 10.1016/s0028-3770 (05)83487-3. PMID 16292170.
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[14]	Sérgio Reis Filho, J., et al. Oligodendrogliomas: estudo anatomopatológico e clínico de 15 casos. Arq. Neuro-Psiquiatr. 57 (2A): 249-54. doi: 10.1590/S0004-282X1999000200013 . PMID:10412525.
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APA Style

Mauricio Vaillant Amarante, Ozinelia Pedroni Batista, Camilia Lampier Lutzke, Shirley Kempin Quiqui. (2019). Patient with Refractory Epilepsy Associated with Oligondendroglioma. Clinical Neurology and Neuroscience, 3(2), 43-45. https://doi.org/10.11648/j.cnn.20190302.13

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ACS Style

Mauricio Vaillant Amarante; Ozinelia Pedroni Batista; Camilia Lampier Lutzke; Shirley Kempin Quiqui. Patient with Refractory Epilepsy Associated with Oligondendroglioma. Clin. Neurol. Neurosci. 2019, 3(2), 43-45. doi: 10.11648/j.cnn.20190302.13

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AMA Style

Mauricio Vaillant Amarante, Ozinelia Pedroni Batista, Camilia Lampier Lutzke, Shirley Kempin Quiqui. Patient with Refractory Epilepsy Associated with Oligondendroglioma. Clin Neurol Neurosci. 2019;3(2):43-45. doi: 10.11648/j.cnn.20190302.13

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@article{10.11648/j.cnn.20190302.13,
  author = {Mauricio Vaillant Amarante and Ozinelia Pedroni Batista and Camilia Lampier Lutzke and Shirley Kempin Quiqui},
  title = {Patient with Refractory Epilepsy Associated with Oligondendroglioma},
  journal = {Clinical Neurology and Neuroscience},
  volume = {3},
  number = {2},
  pages = {43-45},
  doi = {10.11648/j.cnn.20190302.13},
  url = {https://doi.org/10.11648/j.cnn.20190302.13},
  eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.cnn.20190302.13},
  abstract = {Oligodendroglioma is a rare form of primary brain tumor, accounting for about 2-5% of intracranial tumors, being more common in adult males but rare in children, accounting for about 1-2% of all primary brain tumors in children. It originates from oligodendrocytes or glial precursor cells and exhibits infiltrative and slow growth. They can be classified in two grades (Grade II and Grade III), where Grade II are low grade tumors and have tumor cells that grow slowly and invade nearby normal tissue, and Grade III are malignant and have rapidly growing tumors. It has low growth and 50-80% of cases first symptom is seizures. A seizure is a symptom that requires a rapid solution usually requiring empirical treatment at the initial time to cease seizures and promote some well-being for the patient's routine. Seizures can cause a lot of damage to the patient's life, especially if the patient is a child who does not know what to do and what to do. Depending on the intensity and frequency of seizure episodes, the patient may experience fractures with falls, may suffer discrimination and prejudice at school. The causes behind refractory epilepsy are diverse, so whenever a patient is found to be refractory to drug treatment, the origin of seizures should be investigated early, it is not enough to stop at empirical treatment.},
 year = {2019}
}

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TY  - JOUR
T1  - Patient with Refractory Epilepsy Associated with Oligondendroglioma
AU  - Mauricio Vaillant Amarante
AU  - Ozinelia Pedroni Batista
AU  - Camilia Lampier Lutzke
AU  - Shirley Kempin Quiqui
Y1  - 2019/06/20
PY  - 2019
N1  - https://doi.org/10.11648/j.cnn.20190302.13
DO  - 10.11648/j.cnn.20190302.13
T2  - Clinical Neurology and Neuroscience
JF  - Clinical Neurology and Neuroscience
JO  - Clinical Neurology and Neuroscience
SP  - 43
EP  - 45
PB  - Science Publishing Group
SN  - 2578-8930
UR  - https://doi.org/10.11648/j.cnn.20190302.13
AB  - Oligodendroglioma is a rare form of primary brain tumor, accounting for about 2-5% of intracranial tumors, being more common in adult males but rare in children, accounting for about 1-2% of all primary brain tumors in children. It originates from oligodendrocytes or glial precursor cells and exhibits infiltrative and slow growth. They can be classified in two grades (Grade II and Grade III), where Grade II are low grade tumors and have tumor cells that grow slowly and invade nearby normal tissue, and Grade III are malignant and have rapidly growing tumors. It has low growth and 50-80% of cases first symptom is seizures. A seizure is a symptom that requires a rapid solution usually requiring empirical treatment at the initial time to cease seizures and promote some well-being for the patient's routine. Seizures can cause a lot of damage to the patient's life, especially if the patient is a child who does not know what to do and what to do. Depending on the intensity and frequency of seizure episodes, the patient may experience fractures with falls, may suffer discrimination and prejudice at school. The causes behind refractory epilepsy are diverse, so whenever a patient is found to be refractory to drug treatment, the origin of seizures should be investigated early, it is not enough to stop at empirical treatment.
VL  - 3
IS  - 2
ER  -

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Author Information

Mauricio Vaillant Amarante

Department of Family and Community Health Strategy, Municipal Government of Domingos Martins, Domingos Martins, Espírito Santo, Brazil
Ozinelia Pedroni Batista

Department of Family and Community Health Strategy, Municipal Government of Domingos Martins, Domingos Martins, Espírito Santo, Brazil
Camilia Lampier Lutzke

Department of Family and Community Health Strategy, Municipal Government of Domingos Martins, Domingos Martins, Espírito Santo, Brazil
Shirley Kempin Quiqui

Department of Family and Community Health Strategy, Municipal Government of Domingos Martins, Domingos Martins, Espírito Santo, Brazil

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APA Style

Mauricio Vaillant Amarante, Ozinelia Pedroni Batista, Camilia Lampier Lutzke, Shirley Kempin Quiqui. (2019). Patient with Refractory Epilepsy Associated with Oligondendroglioma. Clinical Neurology and Neuroscience, 3(2), 43-45. https://doi.org/10.11648/j.cnn.20190302.13

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ACS Style

Mauricio Vaillant Amarante; Ozinelia Pedroni Batista; Camilia Lampier Lutzke; Shirley Kempin Quiqui. Patient with Refractory Epilepsy Associated with Oligondendroglioma. Clin. Neurol. Neurosci. 2019, 3(2), 43-45. doi: 10.11648/j.cnn.20190302.13

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AMA Style

Mauricio Vaillant Amarante, Ozinelia Pedroni Batista, Camilia Lampier Lutzke, Shirley Kempin Quiqui. Patient with Refractory Epilepsy Associated with Oligondendroglioma. Clin Neurol Neurosci. 2019;3(2):43-45. doi: 10.11648/j.cnn.20190302.13

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@article{10.11648/j.cnn.20190302.13,
  author = {Mauricio Vaillant Amarante and Ozinelia Pedroni Batista and Camilia Lampier Lutzke and Shirley Kempin Quiqui},
  title = {Patient with Refractory Epilepsy Associated with Oligondendroglioma},
  journal = {Clinical Neurology and Neuroscience},
  volume = {3},
  number = {2},
  pages = {43-45},
  doi = {10.11648/j.cnn.20190302.13},
  url = {https://doi.org/10.11648/j.cnn.20190302.13},
  eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.cnn.20190302.13},
  abstract = {Oligodendroglioma is a rare form of primary brain tumor, accounting for about 2-5% of intracranial tumors, being more common in adult males but rare in children, accounting for about 1-2% of all primary brain tumors in children. It originates from oligodendrocytes or glial precursor cells and exhibits infiltrative and slow growth. They can be classified in two grades (Grade II and Grade III), where Grade II are low grade tumors and have tumor cells that grow slowly and invade nearby normal tissue, and Grade III are malignant and have rapidly growing tumors. It has low growth and 50-80% of cases first symptom is seizures. A seizure is a symptom that requires a rapid solution usually requiring empirical treatment at the initial time to cease seizures and promote some well-being for the patient's routine. Seizures can cause a lot of damage to the patient's life, especially if the patient is a child who does not know what to do and what to do. Depending on the intensity and frequency of seizure episodes, the patient may experience fractures with falls, may suffer discrimination and prejudice at school. The causes behind refractory epilepsy are diverse, so whenever a patient is found to be refractory to drug treatment, the origin of seizures should be investigated early, it is not enough to stop at empirical treatment.},
 year = {2019}
}

Copy | Download

TY  - JOUR
T1  - Patient with Refractory Epilepsy Associated with Oligondendroglioma
AU  - Mauricio Vaillant Amarante
AU  - Ozinelia Pedroni Batista
AU  - Camilia Lampier Lutzke
AU  - Shirley Kempin Quiqui
Y1  - 2019/06/20
PY  - 2019
N1  - https://doi.org/10.11648/j.cnn.20190302.13
DO  - 10.11648/j.cnn.20190302.13
T2  - Clinical Neurology and Neuroscience
JF  - Clinical Neurology and Neuroscience
JO  - Clinical Neurology and Neuroscience
SP  - 43
EP  - 45
PB  - Science Publishing Group
SN  - 2578-8930
UR  - https://doi.org/10.11648/j.cnn.20190302.13
AB  - Oligodendroglioma is a rare form of primary brain tumor, accounting for about 2-5% of intracranial tumors, being more common in adult males but rare in children, accounting for about 1-2% of all primary brain tumors in children. It originates from oligodendrocytes or glial precursor cells and exhibits infiltrative and slow growth. They can be classified in two grades (Grade II and Grade III), where Grade II are low grade tumors and have tumor cells that grow slowly and invade nearby normal tissue, and Grade III are malignant and have rapidly growing tumors. It has low growth and 50-80% of cases first symptom is seizures. A seizure is a symptom that requires a rapid solution usually requiring empirical treatment at the initial time to cease seizures and promote some well-being for the patient's routine. Seizures can cause a lot of damage to the patient's life, especially if the patient is a child who does not know what to do and what to do. Depending on the intensity and frequency of seizure episodes, the patient may experience fractures with falls, may suffer discrimination and prejudice at school. The causes behind refractory epilepsy are diverse, so whenever a patient is found to be refractory to drug treatment, the origin of seizures should be investigated early, it is not enough to stop at empirical treatment.
VL  - 3
IS  - 2
ER  -

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