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Relevant bibliographies by topics / Supratentorial Neoplasms

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Academic literature on the topic 'Supratentorial Neoplasms'

Author: Grafiati

Published: 4 June 2021

Last updated: 28 July 2025

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Journal articles on the topic "Supratentorial Neoplasms"

1

Shuangshoti, Shanop, Elisabeth J. Rushing, Hernando Mena, Cara Olsen, and Glenn D. Sandberg. "Supratentorial extraventricular ependymal neoplasms." Cancer 103, no. 12 (2005): 2598–605. http://dx.doi.org/10.1002/cncr.21111.

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2

Patil, Prashanth G., KM Nataraj, and Shaik Hussain Saheb. "Study of Supratentorial Tumours by Computed Tomography." Asian Journal of Medical Radiological Research 8, no. 1 (2020): 114–21. http://dx.doi.org/10.47009/ajmrr.2020.8.1.21.

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Background: Brain neoplasms may be classified by the location of supratentorial, infratentorial and midline tumours. Of the supratentorial neoplasms, meningiomas are the most frequent extra-axial neoplasms. CT has become the most important diagnostic procedure in evaluating patients suspected of harboring an intracranial tumor. It is still considered the basic radiologic study since it gives specific information for the management of brain tumours and is minimally invasive. The purpose of this study was to assess the distribution, features, localization and extent of supratentorial neoplasms.

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Shady, Joseph A., Peter McL Black, William J. Kupsky, et al. "Seizures in Children with Supratentorial Astroglial Neoplasms." Pediatric Neurosurgery 21, no. 1 (1994): 23–30. http://dx.doi.org/10.1159/000120810.

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4

Bradley, William G. "Supratentorial neoplasms, including the sella and parasellar region." Topics in Magnetic Resonance Imaging 1, no. 2 (1989): 16???36. http://dx.doi.org/10.1097/00002142-198903000-00005.

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5

Moss, David S., Stephen J. Haines, Arnold S. Leonard, and Louis P. Dehner. "Congenital Supratentorial and Infratentorial Peripheral Neurogenic Tumor: A Clinical, Ultrastructural, and Immunohistochemical Study." Neurosurgery 19, no. 3 (1986): 426–33. http://dx.doi.org/10.1227/00006123-198609000-00015.

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Abstract Congenital neoplasms of the central nervous system are extremely rare, although they have been well documented since the earliest reports from the mid-19th century. Medulloblastoma, other primitive neuroectodermal tumors, and various types of gliomas have comprised the majority of cases. This report describes a highly unusual infratentorial and supratentorial tumor presenting as a scalp mass in a neonate who experienced in utero distress. The supratentorial mass extended through a defect in the skull to the parietooccipital lobe, and the infratentorial aspect involved the 9th and 10th

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6

Rosenberg, David M., Brett W. Geever, Akash S. Patel, et al. "Supratentorial and Infratentorial Approaches to Pineal Surgery: A Database Analysis." Journal of Neurological Surgery Part B: Skull Base 80, no. 04 (2018): 364–70. http://dx.doi.org/10.1055/s-0038-1675231.

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Objectives Neoplasms involving the pineal gland are rare. When they do occur, tumor resection is anatomically challenging and is traditionally addressed by either a supratentorial or an infratentorial approach. To date, no large, multicenter studies have been performed that systematically analyze outcomes comparing these two approaches. This study aimed to evaluate outcomes for patients undergoing pineal neoplasm resection, comparing supratentorial and infratentorial approaches. Design Retrospective database review. Setting Multi-institutional database. Participants From 2005 to 2016, 60 patie

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7

Dash, Rajesh C., James M. Provenzale, Rodney D. McComb, Deborah A. Perry, Darryl C. Longee, and Roger E. McLendon. "Malignant Supratentorial Ganglioglioma (Ganglion Cell–Giant Cell Glioblastoma)." Archives of Pathology & Laboratory Medicine 123, no. 4 (1999): 342–45. http://dx.doi.org/10.5858/1999-123-0342-msggcg.

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Abstract Background.—From both epidemiologic and pathologic viewpoints, gangliogliomas exhibiting components of giant cell glioblastomas are extraordinary neoplasms. We report herein the case of a 6-year-old girl who presented initially with a World Health Organization grade IV anaplastic ganglioglioma (a mixed ganglion cell tumor–giant cell glioblastoma). Despite aggressive management, the patient died of disease in a relatively short period. Methods.—Formalin-fixed, paraffin-embedded tissue blocks were sectioned at 5 μm for histochemical and immunohistochemical analyses. Hematoxylin-eosin–st

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8

Labuschagne, Jason John. "5-Aminolevulinic Acid–Guided Surgery for Recurrent Supratentorial Pediatric Neoplasms." World Neurosurgery 141 (September 2020): e763-e769. http://dx.doi.org/10.1016/j.wneu.2020.06.019.

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9

Gor, Mohit B., Kuldeepsinh D. Mori, Mehul N. Bavishi, et al. "Evaluation of Supratentorial Brain Neoplasms - A Cross Sectional Study from a Tertiary Care Hospital, Surendranagar, Gujarat." Journal of Evidence Based Medicine and Healthcare 8, no. 26 (2021): 2253–59. http://dx.doi.org/10.18410/jebmh/2021/421.

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BACKGROUND Brain tumours represents 1.7 % of all cancers and contributes 1.8 % of all cancer deaths. Of all the brain tumours, 80 % are supratentorial.1 Magnetic resonance imaging (MRI) is an important modality, having higher sensitivity for detecting intracranial pathology. Multiplanar imaging is possible with MRI which helps in detection, localization and characterization of the lesion. MRI examination has helped in early diagnosis, accurate localization of the tumour, with prompt initiation of appropriate medical or surgical therapy. Recent advances like magnetic resonance (MR) spectroscopy

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10

Telemi, Edvin, Nikolay L. Martirosyan, Mauricio J. Avila, Ashley L. Lukefahr, Christopher Le, and G. Michael Lemole. "Suprasellar pleomorphic xanthoastrocytoma: A case report." Surgical Neurology International 10 (April 24, 2019): 72. http://dx.doi.org/10.25259/sni-83-2019.

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Background: Pleomorphic xanthoastrocytoma (PXA) is a rare form of astrocytic neoplasm most commonly found in children and young adults. This neoplasm, which is classified as a Grade II tumor by the World Health Organization classification of tumors of the central nervous system, carries a relatively favorable outcome. It is usually found supratentorially in cortical regions of the cerebral hemispheres, and as such, presenting symptoms are similar to other supratentorial cortical neoplasms; with seizures being a common initial symptom. Due to the rarity of this type of neoplasm, PXA arising els

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Books on the topic "Supratentorial Neoplasms"

1

Deutsche Gesellschaft für Neurochirurgie. Tagung. Intracranial angiomas ; Neurosurgical intensive care ; Supratentorial tumors in children. Springer-Verlag, 1991.

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2

(Editor), Wolfgang J. Bock, C. Lumenta (Editor), Mario Brock (Editor), and M. Klinger (Editor), eds. Intracranial Angiomas - Neurosurgical Intensive Care (Advances in Neurosurgery). Springer-Verlag Berlin and Heidelberg GmbH & Co. K, 1991.

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3

Brock, M., Wolfgang Joachim Bock, and Ch Lumenta. Intracranial Angiomas/Neurosurgical Intensive Care/Supratentorial Tumors in Children: Proceedings of the 4th Annual Meeting of the Deutsche Gesellsc (Advances in Neurosurgery). Springer, 1991.

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Book chapters on the topic "Supratentorial Neoplasms"

1

"1 Supratentorial Brain Neoplasms." In Essentials of Clinical MR, edited by Val M. Runge and John N. Morelli. Georg Thieme Verlag, 2011. http://dx.doi.org/10.1055/b-0034-75408.

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2

"35. Supratentorial Nonglial Hemispheric Neoplasms." In Principle and Practice of Pediatric Neurosurgery, edited by Leland Albright, Ian Pollack, and David Adelson. Georg Thieme Verlag, 2015. http://dx.doi.org/10.1055/b-0034-98075.

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"30 Supratentorial Hemispheric Nonglial Neoplasms." In Principles and Practice of Pediatric Neurosurgery, edited by Leland Albright, Ian F. Pollack, and David Adelson. Georg Thieme Verlag, 2008. http://dx.doi.org/10.1055/b-0034-56407.

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4

Spreen, Otfried, Anthony H. Risser, and Dorothy Edgell. "Focal Neurological Disorders." In Developmental Neuropsychology. Oxford University PressNew York, NY, 1995. http://dx.doi.org/10.1093/oso/9780195067361.003.0019.

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Abstract This chapter deals with some pediatric neurological disease processes that have not been discussed in previous chapters, such as brain tumors and cerebrovascular conditions. These conditions are not very common in infancy and early childhood, but they do pose a special challenge to the neuropsychologist, given both the tenuousness of the child’s neurological condition and the seriousness of concurrent secondary medical problems. Determining the integrity of mental functioning before and after surgical intervention, the influences of radiotherapy and chemotherapy on cognitive ability,

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5

Johnson, Christopher. "Pediatric Neurologic Radiology." In Ultrasound Guided Procedures and Radiologic Imaging for Pediatric Anesthesiologists, edited by Anna Clebone, Joshua H. Finkle, and Barbara K. Burian. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780190081416.003.0015.

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Chapter 15 examines radiologic images for common pediatric neurologic disorders. These include head and neck disorders such as choanal atresia and congenital piriform aperture stenosis, branchial cleft cysts, thyroglossal duct cyst, fibromatosis colli, and retinoblastoma. The chapter goes on to look at spine diseases such as tethered cord, spinal dysraphism, caudal regression, pars interarticularis defect, and ventriculus terminalis. Brain abnormalities examined include germinal matrix hemorrhage, periventricular leukomalacia, craniosynostosis, and TORCH infection. Intracranial tumors looked a

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Parisi, Joseph E., Hernando Mena, Bernd W. Scheithauer, and Lucy B. Rorke. "CNS Tumors (Excluding Pituitary, PNET, and Embryonal Tumors)." In Principles And Practice Of Neuropathology. Oxford University PressNew York, NY, 2003. http://dx.doi.org/10.1093/oso/9780195125894.003.0016.

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Abstract Gliomas, principally astrocytomas, account for the majority of brain tumors. These intrinsic tumors are derived from neuroectoderm and are classified on the basis of the predominant cell type (astrocyte, oligodendrocyte, or ependymal cell). Although the term glioma applies to all tumors of this group, in practice, glioma usually refers to an infiltrative glial tumor, generally a diffuse astrocytoma or oligodendroglioma. Less commonly, the term glioma has been applied to all tumors of neuroepithelial origin, including those composed of undifferentiated cells, of neuronal elements, and

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Conference papers on the topic "Supratentorial Neoplasms"

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Silva, Matheus Alves da, Eduardo Mesquita de Souza, Rafael Bragança Rodrigues Matias, et al. "Subacute fever and torpor in a hematological patient revealing atypical CLIPPERS with supratentorial involvement: a case report." In XIV Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2023. http://dx.doi.org/10.5327/1516-3180.141s1.403.

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Case report: A 62-year-old patient was transferred from another hospital with complaints of subacute torpor and fever two months after an allogeneic bone marrow transplant. He had the diagnosis of chronic myelomonocytic leukemia type 2 four years before the beginning of the neurological symptoms. The disease remained stable for two years after the diagnosis, but progressed and he was submitted to a bone marrow transplant. The complications during the procedure were a febrile neutropenia, that resolved with a cycle of antibiotics, and a reactivation of cytomegalovirus (CMV) infection (he had a

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