40,744 results match your criteria: "Hydrocephalus"

Technique and protocol for bedside neuroendoscopic lavage for post-hemorrhagic hydrocephalus: technical note.

Childs Nerv Syst

December 2024

Division of Neurosurgery, Department of Surgery, Children's Hospital of Philadelphia, Hub for Clinical Collaboration, 3500 Civic Center Boulevard, 10th floorfloor, Philadelphia, PA, 19104, USA.

Neuroendoscopic lavage (NEL) is a time-limited neurosurgical intervention that removes intraventricular blood in post-hemorrhagic hydrocephalus (PHH). Preterm neonates are medically complex and fragile, often precluding neurosurgical procedures due to concerns such as extubation risk and body temperature instability during even routine clinical care. In addition, transportation to the operating room can be difficult and risky.

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Objective: The Endoscopic Third Ventriculostomy Success Score (ETVSS) is a useful decision-making heuristic when considering the probability of surgical success, defined traditionally as no repeat cerebrospinal fluid diversion surgery needed within 6 months. Nonetheless, the performance of the logistic regression (LR) model in the original 2009 study was modest, with an area under the receiver operating characteristic curve (AUROC) of 0.68.

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Isolated abducens nerve palsy (IANP), caused by secondary communicating hydrocephalus, has been rarely documented; in addition, its mechanism and appropriate treatment are not understood well. This study presents a case of bilateral IANP with hydrocephalus in a 62-year-old man who was successfully treated with cerebrospinal fluid (CSF) diversion to correct an enlarged retroclival space during the follow-up of recurrent brain tumor in the right parieto-occipital lobe. The patient was treated with three resections, temozolomide, and irradiation before developing IANP.

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Impacts of type 1 Chiari malformation on elderly.

Surg Neurol Int

November 2024

Department of Neurosurgery, Hannover Medical School, Hannover, Germany.

Background: This study aims to evaluate the surgical outcomes of elderly patients with Chiari malformation (CM) who underwent suboccipital craniectomy (SC) with duraplasty (DP) or dural splitting (DS). The focus is on symptom relief, changes in syrinx size, hospital admission duration, and postoperative complications.

Methods: A retrospective study was performed to evaluate the outcomes of elderly CM patients who underwent SC with DP or dural splitting (DS).

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Background: Gram-positive opportunistic bacteria of the species are responsible for a large spectrum of infections, such as pneumonia, skin infections, and more widespread conditions, including brain abscesses.

Case Description: A 67-year-old male patient suffered from headache, gait disorder, and vertigo for a week before admission to our department. An enhanced magnetic resonance imaging scan revealed a mediosagittal hyperintense infratentorial lesion with concomitant compression of the fourth ventricle.

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Massive intratumoral hemorrhage following ventriculoperitoneal shunting procedure in an 8-year-old boy: A case report.

Surg Neurol Int

November 2024

Department of Neurosurgery, Dr. Soetomo General Hospital/Faculty of Medicine, Airlangga University, Surabaya, East Java, Indonesia.

Background: Pineal region tumors comprise 0.4% of all central nervous system tumors in adults and 2.8% in children aged up to 19 years.

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Background: Intracranial lipomas are rare, benign lesions with no neoplastic origin. Most affected patients are asymptomatic and are typically pediatric or young adults. We describe a case of a child with a quadrigeminal plate lipoma presenting with seizures and hydrocephalus.

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Effects of cerebral venous outflow patterns on functional outcome in space-occupying cerebellar infarction.

Clin Neurol Neurosurg

January 2025

Departments of Neurology, Korea University Ansan Hospital, Korea University College of Medicine, Ansan, South Korea. Electronic address:

Background: Space-occupying cerebellar infarction can be catastrophic, leading to brainstem compression, transtentorial herniation, and obstructive hydrocephalus. Herein, we investigated the association between the venous outflow pattern based on transverse sinus (TS) shape and the outcome of space-occupying cerebellar infarction.

Methods: Patients with space-occupying cerebellar infarctions were enrolled, and data on baseline demographics, clinical factors, and venous outflow patterns, including the type of TS were collected.

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Article Synopsis
  • A 58-year-old man with meningoencephalitis caused by a brain-eating amoeba died 33 days after symptoms began, highlighting the severity and limited treatment options for this condition.
  • The study introduced ventriculoscopy as a surgical technique to observe and treat the extensive inflammatory response and manage complications like hydrocephalus and intracranial hypertension.
  • Despite the patient's death from brainstem hemorrhage, the case emphasizes the importance of surgical interventions in diagnosing and managing amoebic encephalitis, calling for ongoing research to improve treatment strategies.
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Article Synopsis
  • Partial 17q duplication is a rare chromosome abnormality linked to severe developmental issues, intellectual disabilities, and physical anomalies.
  • A case study presented a 7-year-old boy with several health problems, including developmental delays and malformations, and his aborted older brother also exhibited similar abnormalities.
  • The findings provide insights into the clinical characteristics and fetal implications of 17q25 microduplication related to a maternal genetic translocation.
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PIK3CA-Related Overgrowth Spectrum: Exploring Brain Growth From Fetal to Infant.

Pediatr Neurol

November 2024

Department of Neonatology, Unidade Local de Saúde de Vila Nova de Gaia, Vila Nova de Gaia, Portugal.

Article Synopsis
  • MCAP (Megalencephaly-capillary malformation-polymicrogyria syndrome) is a rare neurological disorder caused by mutations in the PIK3CA gene, leading to abnormal brain growth, vascular issues, and body overgrowth.
  • A clinical report details an infant diagnosed with MCAP, who showed signs of the disorder from prenatal imaging, which identified megalencephaly and a confirmed PIK3CA mutation postnatally, followed by early medical interventions.
  • Despite these interventions, the patient faced ongoing challenges such as macrocrania, hydrocephalus, and neurodevelopmental delays, highlighting the importance of multidisciplinary care and monitoring to manage the complexities of the disorder and emphasizing potential future therapies for better outcomes.
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Correction: Effects of aging on hydrocephalus after intraventricular hemorrhage.

Fluids Barriers CNS

December 2024

Department of Neurosurgery, University of Michigan, R5018 Biomedical Science Research Building, 109 Zina Pitcher Place, Ann Arbor, MI, 48109‑2200, USA.

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Purpose: Chiari malformation type II (CM-II) is a congenital anomaly commonly associated with myelomeningocele (MMC), a severe form of open spina dysraphism. This study aimed to evaluate both supratentorial and infratentorial volumes in MMC infants with and without CM-II.

Methods: We conducted a single-center, retrospective study of 52 MMC infants treated between April 2006 and July 2023.

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Therapeutic Strategies in Neurocutaneous Melanocytosis.

Anticancer Res

December 2024

Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA, U.S.A.

Article Synopsis
  • * The condition is usually fatal if symptoms appear, with a high chance of the brain lesions becoming malignant, especially in those with larger skin nevi.
  • * Current treatments focus on palliative care and aim to manage symptoms, as there is no cure, highlighting the need for ongoing research to develop effective therapies and address this critical medical gap.
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Split notochord syndrome (SNS) is a rare congenital anomaly characterized by incomplete midline notochordal integration during gastrulation, leading to segmental clefts of the spine. This case report describes a female patient with symptomatic cervico-dorsal SNS associated with a neurenteric cyst (NEC), intrathoracic gut duplication, and secondary hydrocephalus. Multistep surgical interventions were performed, including hydrocephalus management, excision of the cyst and gut duplication, and detethering with sectioning of the filum.

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Central Neurocytoma in a Teenager, a Rare Cause of Hemiplegia, and a Diagnostic Dilemma in a Resource-Poor Setting.

Case Rep Pathol

March 2024

Department of Pathology, School of Medical Sciences, University of Cape Coast, Cape Coast Teaching Hospital, Cape Coast, Ghana.

Article Synopsis
  • - Central neurocytoma is a benign brain tumor commonly found in the lateral ventricles, leading to symptoms like headaches and visual issues, particularly in young patients.
  • - An 18-year-old male presented with serious symptoms including seizures and unconsciousness, but due to the healthcare limitations, imaging studies weren’t conducted before his passing; an autopsy later confirmed the diagnosis of central neurocytoma.
  • - The study highlights challenges in differentiating central neurocytoma from other similar tumors, emphasizing the importance of specific lab tests to guide treatment and predict outcomes.
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[Differential expression profile of miRNAs in maternal amniotic fluid exosomes in fetuses with isolated ventriculomegaly].

Nan Fang Yi Ke Da Xue Xue Bao

November 2024

Department of Obstetrics and Gynecology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.

Objective: To investigate the role of miRNAs in maternal amniotic fluid exosomes in development of isolated ventriculomegaly (VM) in fetuses.

Methods: Amniotic fluid samples were collected from 9 cases of moderate isolated VM and 8 normal control cases to extract exosomal miRNA, and miRNA sequencing technique was used to identify differentially expressed miRNAs between the two groups. Three miRNAs with significant differential expression between the two groups, whose high expression was associated with VM, were selected for verification with RT-qPCR.

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Background: This study examined the impact of neurosurgeons' experience on surgical timing and outcomes in aneurysmal subarachnoid hemorrhage (aSAH) and questioned the adherence to early surgery as recommended by recent guidelines.

Methods: A retrospective analysis of 196 aSAH patients treated between 2013 and 2020 was conducted. Variables included age, sex, initial Glasgow Coma Scale (GCS) scores, World Federation of Neurological Surgeons grades, Fisher's grades, rebleeding, hydrocephalus, and preoperative-postoperative neurological status.

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Background: "Dangling choroid" is a prenatal sonographic marker of ventriculomegaly that measures the angle of choroid plexus (ChP) displacement in the lateral ventricle. To the authors' knowledge, postnatal sequelae related to this pathology, besides hydrocephalus, have never been reported.

Observations: A female fetus was diagnosed with bilateral ventriculomegaly.

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Choroid plexus tumors in adults: a retrospective mono-institutional study.

Neurol Sci

December 2024

Neuroncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.

Purpose: Choroid plexus tumors (CPT) are rare entities, and even rarer in adulthood.

Methods: A retrospective consecutive series of 24 adult CPT patients was reviewed.

Results: We described 24 adult CPTs.

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Purpose: Germinal matrix hemorrhage/intraventricular hemorrhage (GMH-IVH) affects primarily preterm infants and causes significant morbidity and mortality. Health disparities are a reality for underserved populations, such as those rural patients. As our institution serves a substantial portion of rural patients, we examined mortality rates and rates of permanent cerebrospinal fluid (CSF) diversion in newborns with GMH-IVH.

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Purpose: To review the current literature, to provide a foundation of knowledge on strabismus surgery in patients with developmental delay, and to present results from the authors' personal experience.

Methods: The following terms were searched on PubMed: strabismus surgery, mental delay, developmental delay, Down syndrome, Angelman syndrome, cerebral palsy, hydrocephalus, Williams syndrome, fragile X syndrome, and fetal alcohol syndrome. Surgical outcomes were analyzed and discussed; only English articles were included.

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Tuberculous meningitis as an underlying cause of rapid neurological deterioration in a patient with a history of psychiatric disorder: Clinical case report.

Diagn Microbiol Infect Dis

November 2024

Unidad de Investigación Biomédica Zacatecas, Instituto Mexicano del Seguro Social, Interior Alameda No. 45 Zac., Zacatecas 98000, Mexico. Electronic address:

Tuberculous meningitis (TBM), the least common of extrapulmonary tuberculosis presentations, one of the most severe. Highly prevalent in immunosuppressed individuals it is associated with high mortality and significant neurological sequelae. TBM main complications are hydrocephalus, increased intracranial pressure, and compromised blood flow with poor prognosis.

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