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Relevant bibliographies by topics / Intraventricular Tumor

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Academic literature on the topic 'Intraventricular Tumor'

Author: Grafiati

Published: 7 June 2025

Last updated: 26 June 2025

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Journal articles on the topic "Intraventricular Tumor"

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Fernández Ochoa, Diana, and Segundo Cabrera Hipólito. "Tumor intraventricular: subependinoma." Interciencia médica 11, no. 1 (2021): 49–52. http://dx.doi.org/10.56838/icmed.v11i1.37.

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Se describe el caso de un paciente que curso con hidrocefalia sintomática debido a la presencia de un tumor intraventricular (subependimoma), se realiza comparación del caso con los hallazgos que se presentan usualmente este tumor en tomografía, resonancia, histopatología e inmunohistoquímica.

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Ahmad, Faiz Uddin, Ashish Suri, Ashok Kumar Mahapatra, et al. "Intraventricular rhabdoid tumor." Indian Journal of Pediatrics 72, no. 8 (2005): 693–96. http://dx.doi.org/10.1007/bf02724079.

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Souweidane, Mark M., and Neal Luther. "Endoscopic resection of solid intraventricular brain tumors." Journal of Neurosurgery 105, no. 2 (2006): 271–78. http://dx.doi.org/10.3171/jns.2006.105.2.271.

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Object Endoscopic removal of intraventricular brain tumors is well established for cystic tumors such as colloid cysts. Aspiration followed by removal or ablation of the membranous wall is possible given the constituent features of these tumors. It is generally expected that endoscopic removal of solid brain tumors from the intraventricular compartment would impose additional technical demands. In this paper, the feasibility and safety of endoscopic removal of solid intraventricular brain tumors is evaluated. Methods Eighty-one patients who underwent endoscopic management of an intraventricular brain tumor were identified from a prospective database. Of these patients, seven underwent attempted endoscopic surgical removal of a solid primary brain tumor. Patient selection, surgical technique, procedure-related morbidity, and extent of removal were reviewed. Five patients underwent complete resection of a solid intraventricular brain tumor, a treatment option that was based on intraoperative assessment and confirmed by postoperative imaging. No patient experienced any procedure-related morbidity. Of the individuals in whom a total endoscopic resection was successful, there has been no symptomatic or radiological evidence of recurrence (mean follow up 20 months). Maximum tumor diameter ranged from 0.5 to 1.8 cm for patients who underwent complete resection, whereas maximum tumor diameter measured 2.4 and 2.5 cm in the two patients in whom a subtotal excision was performed. Conclusions In select patients, complete endoscopic removal of solid intraventricular brain tumors is possible and safe. Factors that influence the ability of a surgeon to perform a complete endoscopic resection include tumor size, composition, and vascularity. The procedure requires careful patient selection, the use of refined endoscopic instrumentation, and a disciplined surgical technique.

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Otomo, Yuta, Naoki Ikegaya, Akito Oshima, et al. "Superficial siderosis and nonobstructive hydrocephalus due to subependymoma in the ventricle: An illustrative case report." Surgical Neurology International 12 (December 30, 2021): 631. http://dx.doi.org/10.25259/sni_868_2021.

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Background: Intraventricular tumors can generally result in obstructive hydrocephalus as they grow. Rarely, however, some intraventricular tumors develop superficial siderosis (SS) and trigger hydrocephalus, even though the tumor has hardly grown. Here, we present an illustrative case of SS and nonocclusive hydrocephalus caused by subependymoma of the lateral ventricles. Case Description: A 78-year-old man with an intraventricular tumor diagnosed 7 years ago had been suffering from gait disturbance for 2 years. He also developed cognitive impairment. Intraventricular tumors showed little growth on annual magnetic resonance imaging (MRI). MRI T2-star weighted images (T2*WI) captured small intratumoral hemorrhages from the beginning of the follow-up. Three years before, at the same time as the onset of ventricular enlargement, T2*WI revealed low intensity in the whole tumor and cerebral surface. Subsequent follow-up revealed that this hemosiderin deposition had spread to the brain stem and cerebellar surface, and the ventricles had expanded further. Cerebrospinal fluid (CSF) examination revealed xanthochromia. The tumor was completely removed en bloc. Histopathological findings were consistent with those of subependymoma. Although CSF findings improved, SS and hydrocephalus did not improve. Therefore, the patient underwent a lumboperitoneal shunt for CSF diversion after tumor resection. Conclusion: Some intraventricular tumors cause SS and nonobstructive hydrocephalus due to microbleeding, even in the absence of tumor growth. T2*WI and, if necessary, timely CSF examination can allow identification of presymptomatic SS. This follow-up strategy may provide a favorable course by facilitating early intervention in patients with intraventricular lesions, not just subependymomas.

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Alam, Shamsul, AN Wakil Uddin, Mashiur Rahman Majumder, Md Motasimul Hasan, and Anis Ahmed. "Intraventricular Tumor: An Analysis of 18 Cases." Bangladesh Journal of Neuroscience 31, no. 2 (2015): 94–101. http://dx.doi.org/10.3329/bjn.v31i2.57386.

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Objective: To describe the transcallosal and transcortical approach to deal with intraventricular tumors. Methods: Details of the transcallosal and transcortical approach to intraventricular tumors of the lateral and third ventricles were presented. Results: Intraventricular tumors are ideal indications for microscopic neurosurgery. They often cause cerebrospinal fluid (CSF) pathway obstruction, resulting in ventricular dilatation. The general principle of removal of intraventricular tumors was interruption of the blood supply to the tumor and subsequent tumor debulking. In general, a piecemeal resection was performed; however, in some tumors such as meningioma, it was possible to detach the lesion from the surrounding brain tissue and remove it in toto. When the tumor found in the anterior part of the third ventricle, the craniotomy was done at the coronal suture. When the tumor was located in the posterior part, the entry craniotomy was selected more anteriorly in order to pass the foramen of Monro in a straight line. Conclusion: Intraventricular tumors and related CSF pathway obstructions can be safely and effectively treated with micro neurosurgical techniques, either by transcallosal or transcortical approach. The aim should be the total extraction of the tumor with minimum damage and the chosen operative corridor should optimize tumor access and the protection of vulnerable neurovascular structures. Lateral ventricle tumors can be removed via transcortical approach when having hydrocephalus which provides a wider and more direct approach to the tumor than the transcallosal one. It allows the surgeon to achieve good functional outcome and maximum excision of the tumor. Transcallosal is an excellent midline exposure with preserving the callosomerginal and pericallosal arteriesto the midline tumor of lateral and 3rd ventricles. Bangladesh Journal of Neuroscience 2015; Vol. 31 (2): 94-101

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Mukesh K., Bhaskar. "Intraventricular Arteriovenous Malformation Mimicking Tumor: A Rare Presentation." International Journal of Neurology and Neurosurgery 9, no. 1 (2017): 57–59. http://dx.doi.org/10.21088/ijnns.0975.0223.9117.11.

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Meriem Kajeou, Israe El Maghrebi, Salma Abbas, and Yasser Arkha. "When rarity complicates diagnosis: A rare intraventricular tumor in pediatrics." World Journal of Advanced Research and Reviews 25, no. 2 (2025): 2134–39. https://doi.org/10.30574/wjarr.2025.25.2.0606.

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Introduction: Meningiomas are rare tumors in children, accounting for around 3% of all pediatric brain tumors. Among them, primary intraventricular meningiomas (PIM) are even more exceptional, with an estimated incidence of between 0.5% and 5% of all meningiomas. This article presents a case of intraventricular meningioma in a 7-year-old child, with a review of the literature. Case Report: We report the case of an intraventricular meningioma in a 7-year-old child. He presented with symptoms of intracranial hypertension, and a cerebral MRI revealed an enhanced tumor at the intraventricular level of the right lateral ventricle. After surgical excision, histology showed a WHO grade I transitional meningioma. The postoperative course was favorable, with satisfactory radiological and clinical control. Conclusion: Intraventricular meningiomas are rare in the pediatric population. These tumors are often large and aggressive when they occur in children. The management of these tumors is a surgical challenge.

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Altinörs, Nur, Tarkan Calisaneller, Salih Gülşen, Özlem Özen, and Önder Öngürü. "INTRAVENTRICULAR DYSEMBRYOPLASTIC NEUROEPITHELIAL TUMOR." Neurosurgery 61, no. 6 (2007): E1332—E1333. http://dx.doi.org/10.1227/01.neu.0000306114.08540.aa.

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Abstract OBJECTIVE The most common localization of dysembryoplastic neuroepithelial tumors (DNTs) is the supratentorial cortex, often in the temporal lobe. However, intraventricular localization of a DNT is extremely rare. CLINICAL PRESENTATION A 30-year-old woman presented with a 1-year history of epileptic seizures. The seizures had not been controlled despite standard doses of antiepileptics. INTERVENTION Neuroimaging results demonstrated a lesion located in the occipital horn of the right lateral ventricle. The lesion was totally removed. Based on histopathological and immunohistochemical evaluation, a DNT was diagnosed. Over the course of the next 8 months, the patient's epileptic seizures were under control. The most recent neuroimaging examinations revealed neither residual nor recurrent tumor. CONCLUSION Because DNTs are surgically curable and neither radiotherapy nor chemotherapy is required after surgery, recognition of an intraventricular DNT in this location is extremely important.

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Bell, Sarah L., Nigel J. Suttner, and William Stewart. "An unusual intraventricular tumor." Neuropathology 32, no. 3 (2011): 311–13. http://dx.doi.org/10.1111/j.1440-1789.2011.01247.x.

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Tandon, Nitin, Thomas J. O'Neill, Dennis G. Vollmer, and Min Wang. "Intraventricular occurrence of a melanocytoma." Journal of Neurosurgery 109, no. 3 (2008): 480–85. http://dx.doi.org/10.3171/jns/2008/109/9/0480.

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Melanocytomas are rare tumors of the central nervous system that are believed to arise from leptomeningeal melanocytes. A young girl presented with a contrast-enhancing cystic mass in the temporal horn of the left lateral ventricle. Microsurgical resection of a black-colored vascular tumor supplied by the anterior choroidal artery was performed. Appropriate immunohistochemical staining and electron microscope evaluations were used to confirm the pathological diagnosis. The patient made an excellent recovery; follow-up imaging revealed no recurrent or residual tumor. This is the first documented primary occurrence of a melanocytoma in an intraventricular location. The intraventricular occurrence of this tumor suggests that melanocytes may migrate into the choroidal fissure and may infrequently undergo neoplastic proliferation in that location. This case contains implications for the differential diagnosis of intraventricular tumors.

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Dissertations / Theses on the topic "Intraventricular Tumor"

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Tanaka, Kuniaki. "Direct Delivery of piggyBac CD19 CAR T Cells Has Potent Anti-tumor Activity against ALL Cells in CNS in a Xenograft Mouse Model." Kyoto University, 2021. http://hdl.handle.net/2433/261609.

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Sirisangtragul, Chuleekorn [Verfasser]. "Pharmacokinetics and pharmacodynamics of intraventricularly administered etoposide in brain tumour patients / vorgelegt von Chuleekorn Sirisangtragul." 2006. http://d-nb.info/983748489/34.

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Books on the topic "Intraventricular Tumor"

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Majmundar, Neil, and James K. Liu. Ventricular Tumors. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190696696.003.0009.

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Central neurocytomas are rare benign tumors that are typically located in the lateral ventricles. Because they are typically intraventricular, these tumors tend to present clinically with hydrocephalus. Currently, surgical removal with a gross-total resection is the treatment of choice. Various radiotherapy techniques, including both conventional radiotherapy and stereotactic radiosurgery, have been shown to be useful in cases of residual tumor after subtotal resection and tumor recurrence. This chapter presents a clinical case of central neurocytoma that demonstrates the typical clinical and radiological findings, as well as the diagnostic workup and surgical management of these tumors.

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Sharma, Deepak, and Julia Metzner. Nontraumatic Intracranial Hemorrhage. Edited by Matthew D. McEvoy and Cory M. Furse. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190226459.003.0062.

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Nontraumatic subarachnoid, intraventricular, or intraparenchymal hemorrhage can be caused by either rupture of an aneurysm or arteriovenous malformation or by coagulopathy, hypertension, or vasculitis. Pituitary apoplexy results from spontaneous hemorrhage or infarction into a pituitary tumor. Additionally, anesthesiologists must be prepared to manage intraoperative bleeding during craniotomies. Successful management of nontraumatic intracranial hemorrhage requires (1) careful preoperative evaluation and preparation considering extracranial manifestations of intracranial bleeding; (2) administration of balanced anesthesia to facilitate surgical exposure and neurophysiological monitoring; (3) maintenance of cerebral perfusion by preserving circulating volume, judicious use of blood product transfusion and vasopressors, and avoidance of excessive hyperventilation; and, when possible, (4) providing timely emergence from anesthesia to allow neurological assessment. Close communication between the surgical and anesthesia teams is critical for optimizing the potential for good patient outcomes.

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Sribnick, Eric, and Jeffrey Leonard. Choroid Plexus Tumors. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190696696.003.0004.

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This chapter presents the case of an 11-month-old male with a history of macrocephaly, anorexia, and right upper extremity tremors. His family history was significant for a father with anaplastic astrocytoma. Physical exam was notable for left asymmetric macrocephaly and a full/tense fontanelle. The chapter reviews the differential diagnoses for macrocephaly. Imaging, including magnetic resonance spectroscopy, revealed a highly vascular intraventricular mass with some areas of likely necrosis, suggesting choroid plexus carcinoma. The authors review the preoperative planning and surgical management of this case, including potential complications and their management. Finally, choroid plexus carcinomas are reviewed in light of evidence-based medicine and clinical outcomes.

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Weiner, Howard, and Peter B. Crino. Familial tumour syndromes: tuberous sclerosis complex. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199651870.003.0017.

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Tuberous sclerosis complex (TSC) is a multisystem, genetic disorder that results from mutations in TSC1 or TSC2 genes. Neurological and neuropsychiatric disabilities include epilepsy, intellectual disability, autism, attention deficit disorder, and generalized anxiety. Cortical dysplasias (also known as tubers) are developmental abnormalities of the cerebral cortex that are believed to be responsible for seizures, cognitive disability, and autism. Subependymal giant cell astrocytomas (SEGAs) are intraventricular tumours that can cause hydrocephalus, increased intracranial pressure, and death. TSC results from hyperactivation of the mammalian target of rapamycin (mTOR) pathway in neurons in the brain. This chapter reviews the clinical presentations of TSC as well as diagnostic approaches for epilepsy and SEGAs. It discusses the genetics and cellular pathogenesis of TSC as well as reviewing the link to mTOR signalling. This chapter also presents evidence for different treatment modalities for seizures and SEGAs. It is written for qualified specialist physicians and caregivers.

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Book chapters on the topic "Intraventricular Tumor"

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Kunwar, Sandeep, G. Evren Keles, and Mitchell S. Berger. "Intraventricular and Pineal Region Tumors." In Tumor Neurosurgery. Springer London, 2006. http://dx.doi.org/10.1007/978-1-84628-294-2_13.

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Das, Joe M. "Intraventricular Tumors." In Neuro-Oncology Explained Through Multiple Choice Questions. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-13253-7_21.

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Vigo, Vera, Alejandro Monroy-Sosa, and Roberto Rodriguez-Rubio. "Surgical Treatment of Intraventricular Tumors." In Principles of Neuro-Oncology. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-54879-7_28.

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Collmann, H., E. Kazner, and C. Sprung. "Supratentorial Intraventricular Tumors in Childhood." In Lesions of the Cerebral Midline. Springer Vienna, 1985. http://dx.doi.org/10.1007/978-3-7091-8813-2_11.

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Delfini, Roberto, and Angelo Pichierri. "Transcallosal Approaches to Intraventricular Tumors." In Cranial, Craniofacial and Skull Base Surgery. Springer Milan, 2010. http://dx.doi.org/10.1007/978-88-470-1167-0_7.

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Sandberg, David I., and Faiz Ahmad. "Pediatric Intraventricular Brain Tumors: Endoscopic Neurosurgical Techniques." In Pediatric Cancer. Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-2957-5_15.

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Deopujari, Chandrashekhar, Krishna Shroff, Suhas Malineni, et al. "Intraventricular Tumors: Surgical Considerations in Lateral and Third Ventricular Tumors." In Advances and Technical Standards in Neurosurgery. Springer Nature Switzerland, 2024. http://dx.doi.org/10.1007/978-3-031-53578-9_3.

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Schramm, J., C. Cedzich, and K. Bingham. "Postoperative Results and Complications of Supratentorial, Intraventricular Tumors." In Cerebellar Infarct. Midline Tumors. Minimally Invasive Endoscopic Neurosurgery (MIEN). Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-78801-7_7.

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Souweidane, Mark M. "Endoscopic Management of Intraventricular Brain Tumors in Children." In Neuroendoscopy. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-39085-2_10.

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Verheggen, R., and E. Markakis. "Intraventricular and Intrapontine Vascular Malformations: Symptoms, Surgical Approach, and Postoperative Results." In Cerebellar Infarct. Midline Tumors. Minimally Invasive Endoscopic Neurosurgery (MIEN). Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-78801-7_13.

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Conference papers on the topic "Intraventricular Tumor"

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Bomben, Matteo, Thomas Looi, Naomi Matsuura, and James Drake. "Compression-Aided Millisecond-Scale Cauterization and its Application in Achieving Concurrent Hemostasis During Powered Tissue Resection." In 2025 Design of Medical Devices Conference. American Society of Mechanical Engineers, 2025. https://doi.org/10.1115/dmd2025-1098.

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Abstract Motorized tissue shavers are commonly used to rapidly fragment and remove intraventricular brain tumors during endoscopic neurosurgery. However, a key drawback of these devices is that they cannot be used on vascularized tumors as unmanageable levels of bleeding are encountered when they are fragmented. This problem could be addressed by concurrently applying a radiofrequency (RF) current to cauterize the tumor tissue as it is shaved, but this approach would require that cauterization occur in less than 50 ms. In this work, we investigated whether simultaneous tissue compression paired with a RF current can be used to achieve cauterization in millisecond timescales and then integrated this technique into the design of a combined cautery-shaver mechanism. We began by using both finite element modelling and benchtop experiments to demonstrate that cauterization occurs in timeframes as short as 15 ms if tissue is simultaneously compressed during RF current application. Based on these results, a novel shaver device that compresses and cauterizes tissue just prior to fragmentation was developed. Proof-of-concept prototypes demonstrated the design’s ability to both resect and rapidly cauterize tissue. Finally, we fabricated a fully mechanized version of the device that could execute a single tissue resection cycle on command. Testing on ex vivo brain samples showed that the tool successfully cauterized tissue to the depth necessary for hemostasis while simultaneously resecting a mass of tissue comparable to that removed by existing shaver tools.

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Gladi, Maurizio, Denis Aiudi, Fabio Greco, et al. "Minimally Invasive Surgical Strategies in Intraventricular Tumors: A Single-Institution Preliminary Experience with Tubular Retractors for Intraventricular Meningiomas." In 33rd Annual Meeting North American Skull Base Society. Georg Thieme Verlag KG, 2024. http://dx.doi.org/10.1055/s-0044-1780344.

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Bomben, Matteo, Paul H. Kang, Thomas Looi, Naomi Matsuura, and James Drake. "Development of a Flexible Tissue Resection Device for Robotic Intracranial Tumour Removal." In The Hamlyn Symposium on Medical Robotics. The Hamlyn Centre Imperial College London, 2024. http://dx.doi.org/10.31256/hsmr2024.9.

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In recent decades, use of an endoscopic approach to resect intraventricular brain tumours has increased in frequency given the promise of reduced morbidity and shorter recovery times [1]. This trend has partly been facilitated by the introduction of motorized tissue shavers, which use oscillating blades to fragment the tumour while simultaneously removing these fragments via aspiration [2], [3]. Unfortunately, existing shavers possess straight, rigid, shafts. As a result, the shaver must be angled or pivoted to reach the entirety of a tumour, an action that compresses adjacent brain tissue [4]. Thus, endoscopic tumour resection can damage neurological structures and, due to the limits placed on pivot angle, is associated with incomplete tumour resection. To increase a surgeon’s range-of-motion during endoscopic procedures without relying on tool pivoting, curvilinear neurosurgical robots are being developed. Of particular interest, given its small diameter, is the concentric tube robot (CTR) [5]. CTRs consist of pre- curved, super-elastic tubes that are nested concentrically and translated/rotated to control tip pose. However, existing straight, rigid shavers are not CTR-compatible as they would deform the shape of the pre-curved tubes if inserted through them. As such, the objective of this research is to develop a novel tissue shaver that is flexible and thus CTR-compatible.

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Khatua, Soumen, Vidya Gopalakrishnan, Laurence Cooper, et al. "Abstract CT033: Phase I study of intraventricular infusions of autologous exvivo expanded NK cells in children with recurrent/refractory malignant posterior fossa tumors of the central nervous system." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-ct033.

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Khatua, Soumen, Dean Lee, Laurence Cooper, et al. "Abstract CT216: Phase I study of intraventricular infusions of autologous ex vivo expanded NK cells in children with recurrent/refractory malignant posterior fossa tumors of the central nervous system." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-ct216.

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Khatua, Soumen, Dean Lee, Laurence Cooper, et al. "Abstract CT216: Phase I study of intraventricular infusions of autologous ex vivo expanded NK cells in children with recurrent/refractory malignant posterior fossa tumors of the central nervous system." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-ct216.

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