2/2025
vol. 76
Opis przypadku
Arteriovenous malformation within the velum interpositum
- Department of Pathology, Microbiology and Immunology, Vanderbilt University, United States of America
- Department of Pathology, University of Illinois at Chicago, United States of America
Pol J Pathol 2025; 76 (2): 163-167
Data publikacji online: 2025/09/22
Plik artykułu
1. Chen CY, Chen FH, Lee CC, Lee KW, Hsiao HS. Sonographic characteristics of the cavum velum interpositum. AJNR Am J Neuroradiol 1998; 19: 1631-1635.
2.
Bass J, Takahashi JS. Circadian rhythms: Redox redux. Nature. 2011; 469: 476-478.
3.
Zohdi A, Elkheshin S. Endoscopic anatomy of the velum interpositum: A sequential descriptive anatomical study. Asian J Neurosurg 2012; 7: 12-16.
4.
International Agency for Research on Cancer. WHO Classification of Tumours Editorial Board. Central nervous system tumours. Vol. Central nervous system tumours.WHO Classification of Tumours. WHO, Lyon 2021.
5.
Choque-Velasquez J, Colasanti R, Muhammad S, Chioffi F, Hernesniemi J. Vascular Lesions of the Pineal Region: A Comprehensive Review of the Therapeutic Options. World Neurosurg 2022; 159: 298-313.
6.
Majovsky M, Netuka D, Lipina R, Mracek J, Beneš V. Pineal Apoplexy: A Case Series and Review of the Literature. J Neurol Surg A Cent Eur Neurosurg 2022; 83: 31-38.
7.
Atallah O, Chaurasia B, Badary A, et al. Pineal Apoplexy: Highlighting the Causes, Treatment, and Outcome. J Neurol Surg A Cent Eur Neurosurg 2025; 86: 85-98.
8.
Kim E, Kwon SM. Pineal Cyst Apoplexy: A Rare Complication of Common Entity. Brain Tumor Res Treat 2020; 8: 66-70.
9.
Karthik DK, Khardenavis V, Kulkarni S, Deshpande A. Pineal gland apoplexy mimicking as migraine-like headache. BMJ Case Rep 2018; 2018: bcr2018225187.
10.
Wang CC, Turner J, Steel T. Spontaneous pineal apoplexy in a pineal parenchymal tumor of intermediate differentiation. Cancer Biol Med 2013; 10: 43-46.
11.
Lunsford LD, Maroon JC, Bank WO, Drayer BP, Rosenbaum AE. Localization of velum interpositum AVM with metrizamide ventriculography and simultaneous stereoangiography. Case report. J Neurosurg 1977; 47: 623-625.
12.
Barreau X, Marnat G, Gariel F, Dousset V. Intracranial arteriovenous malformations. Diagn Interv Imaging 2014; 95: 1175- 1186.
13.
Stapf C, Mast H, Sciacca RR, et al. The New York Islands AVM Study: design, study progress, and initial results. Stroke 2003; 34: e29-e33.
14.
International Study of Unruptured Intracranial Aneurysms Investigators. Unruptured intracranial aneurysms – risk of rupture and risks of surgical intervention. N Engl J Med 1998; 339: 1725-1733.
15.
Locksley HB, Sahs AL, Sandler R. Report on the cooperative study of intracranial aneurysms and subarachnoid hemorrhage. 3. Subarachnoid hemorrhage unrelated to intracranial aneurysm and A-V malformation. A study of associated diseases and prognosis. J Neurosurg 1966; 24: 1034-1056.
16.
Goehre F, Jahromi BR, Lehecka M, et al. Posterior Cerebral Artery Aneurysms: Treatment and Outcome Analysis in 121 Patients. World Neurosurg 2016; 92: 521-532.
17.
Rodríguez-Hernández A, Walcott BP, Birk H, Lawton MT. The Superior Cerebellar Artery Aneurysm: A Posterior Circulation Aneurysm with Favorable Microsurgical Outcomes. Neurosurgery 2017; 80: 908-916.
18.
Benjamin JC, Furneaux CE, Scholtz CL. Pineal astrocytoma. Surg Neurol 1985; 23: 139-142.
19.
Kumar P, Tatke M, Sharma A, Singh D. Histological analysis of lesions of the pineal region: a retrospective study of 12 years. Pathol Res Pract 2006; 202: 85-92.
20.
Levidou G, Korkolopoulou P, Agrogiannis G, Paidakakos N, Bouramas D, Patsouris E. Low-grade oligodendroglioma of the pineal gland: a case report and review of the literature. Diagn Pathol 2010; 5: 59.
21.
Hwan Kim Y, Vu PN, Choe SW, et al. Overexpression of Activin Receptor-Like Kinase 1 in Endothelial Cells Suppresses Development of Arteriovenous Malformations in Mouse Models of Hereditary Hemorrhagic Telangiectasia. Circ Res 2020; 127: 1122-1137.
22.
McDonald J, Bayrak-Toydemir P, Pyeritz RE. Hereditary hemorrhagic telangiectasia: an overview of diagnosis, management, and pathogenesis. Genet Med 2011; 13: 607-616.
23.
Hong T, Yan Y, Li J, et al. High prevalence of KRAS/BRAF somatic mutations in brain and spinal cord arteriovenous malformations. Brain 2019; 142: 23-34.
24.
Stefani MA, Sgarabotto Ribeiro D, Mohr JP. Grades of brain arteriovenous malformations and risk of hemorrhage and death. Ann Clin Transl Neurol 2019; 6: 508-514.
25.
Spetzler RF, Ponce FA. A 3-tier classification of cerebral arteriovenous malformations. Clinical article. J Neurosurg 2011; 114: 842-849.
Copyright: © 2025 Polish Association of Pathologists and the Polish Branch of the International Academy of Pathology This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
