2024, Number 1
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Arch Neurocien 2024; 29 (1)
Astrocitoma anaplásico de región pineal, seguimiento a 4 años: reporte de un caso
Castañeda-Aguayo F, Valdéz-Orduño R, Hernández-Salazar M, Hernández-Zamora CI
Language: Spanish
References: 15
Page: 11-14
PDF size: 171.18 Kb.
ABSTRACT
no abstract.
REFERENCES
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Randy S. D’Amico, M.D. et. Al. Pineal region glioblastomasdisplay features of diffuse midline and non-midline gliomas, JNeurooncol. 2018 October ; 140(1): 63–73. doi:10.1007/s11060-018-2931-4.
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Monroy-Sosa Al. Et. Al. 2020, chapter 25: Managementof pineal region tumors, Joham ChoqueVelasquez. Et.Al., Principles of neuro-oncology Brain & Skull Base. https://doi.org/10.1007/978-3-030-54879-7.
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Favero, G.; Bonomini, F.; Rezzani, R. Pineal GlandTumors: A Review. Cancers 2021, 13, 1547. https://doi.org/10.3390/ cancers13071547.
10.Jung Jang, Seon, (2012) A biphasic tumor consisting ofpilocytic astrocytoma with an anaplastic solitary fibrous tumorcomponent in the pineal region: A case report and literature review,Neuropathology, doi:10.1111/j.1440-1789.2012.01347.x.
Almahariq F, Raguz M, Romic D, Dlaka D, Oreskovic D, Sesar P,et al. A biphasic tumor in posterior cranial fossa and the pinealregion in young adult. Surg Neurol Int 2020;11:64.
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