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Child s Nervous System

Subject Areas: Medicine (miscellaneous); ;
Publisher: Springer Berlin Heidelberg - Springer Journals
ISSN: 0256-7040
SJR: 87

LitStream

Journal Article

Long-term sequelae of normocephalic pansynostosis: a rare but insidious entity

Wu, Meagan; Massenburg, Benjamin B.; Reddy, Neil; Romeo, Dominic J.; Ng, Jinggang J.; Taylor, Jesse A.; Swanson, Jordan W.; Bartlett, Scott P.; Lang, Shih-Shan

2024 Child s Nervous System

doi:10.1007/s00381-024-06379-8 pmid:38568218

ObjectivePatients with normocephalic pansynostosis, who have a grossly normal head shape, are often overlooked early in life and present late with elevated intracranial pressure (ICP) requiring timely cranial vault expansion. This study evaluates the long-term clinical outcomes of patients with...
Open Access

Journal Article

Treatment of pediatric intracranial aneurysms: institutional case series and systematic literature review

Brandel, Michael G.; Plonsker, Jillian H.; Rennert, Robert C.; Produturi, Gautam; Saripella, Megana; Wali, Arvin R.; McCann, Carson; Ravindra, Vijay M.; Santiago-Dieppa, David R.; Pannell, J. Scott; Steinberg, Jeffrey A.; Khalessi, Alexander A.; Levy, Michael L.

2024 Child s Nervous System

doi:10.1007/s00381-024-06384-x

IntroductionPediatric intracranial aneurysms (IAs) are rare and have distinct clinical profiles compared to adult IAs. They differ in location, size, morphology, presentation, and treatment strategies. We present our experience with pediatric IAs over an 18-year period using surgical and...
LitStream

Journal Article

Central precocious puberty secondary to postoperative craniopharyngioma: two case reports and a literature review

Zhu, Ruyuan; Wang, Luyao; Zhao, Ling; Liu, Xiaojing

2024 Child s Nervous System

doi:10.1007/s00381-024-06406-8

BackgroundCraniopharyngioma is a common intracranial tumour in children. Clinical manifestations are related to hypothalamic/pituitary deficiencies, visual impairment, and increased intracranial pressure. Defects in pituitary function cause shortages of growth hormone, gonadotropin,...
LitStream

Journal Article

Bleeding solitary SEGA in non-tuberous sclerosis complex adolescent: a case illustration and review of literature

Yindeedej, Vich; Rojnueangnit, Kitiwan; Chotsakulthong, Pasinee; Thamwongskul, Chatchai

2024 Child s Nervous System

doi:10.1007/s00381-024-06382-z pmid:38578478

Subependymal giant cell astrocytoma (SEGA) represents a benign brain tumor occurring in 5–20% of individuals diagnosed with tuberous sclerosis complex (TSC), serving as a major diagnostic criterion. The presence of SEGA in a patient often prompts consideration of TSC as a probable diagnosis,...
Open Access

Journal Article

Staged neurosurgical approach for giant and progressive neonatal arachnoid cysts: a case series and review of the literature

Peraud, Aurelia; Schuler-Ortoli, Marie; Schaal, Matthias; Reister, Frank; Ehrhardt, Harald; Friebe-Hoffmann, Ulrike

2024 Child s Nervous System

doi:10.1007/s00381-024-06385-w pmid:38602531

ObjectivesPrenatally diagnosed complex arachnoid cysts are very rare. While the true prenatal incidence is still unknown, they account for approximately 1% of intracranial masses in newborns. They rarely exhibit rapid growth or cause obstructive hydrocephalus, but if they increase to such a...
Open Access

Journal Article

Occipital nerve stimulation in pediatric patients with refractory occipital neuralgia

Mossner, James; Saleh, Nour B.; Shahin, Maryam N.; Rosenow, Joshua M.; Raskin, Jeffrey S.

2024 Child s Nervous System

doi:10.1007/s00381-024-06376-x pmid:38563970

PurposeOccipital neuralgia (ON) is a disabling problem within the pediatric population. Many of these patients fail medical therapies and continue to suffer without further surgical management. Occipital nerve stimulation (ONS) is used to treat ON in the adult population leading to a 72–89%...
LitStream

Journal Article

Migration of the anal distal end due to ventriculoperitoneal shunt placement: an atypical case report of a 9-month-old infant with tuberculous meningitis and review of the literature

Zarra, Francisco; Shahid, Adnan Hussain; Gandhi, Dhruv Nihal; Salazar, Luis Rafael Moscote; Chaurasia, Bipin

2024 Child s Nervous System

doi:10.1007/s00381-024-06405-9 pmid:38625589

BackgroundVentriculoperitoneal shunt (VPS) represents one of the most classic and widely used treatments for hydrocephalus in pediatric patients. Migration and externalization of the distal end of the catheter through the rectum are extremely rare complications of intestinal perforation with...
Open Access

Journal Article

External ventricular drainage in pediatric patients: indications, management, and shunt conversion rates

Atallah, Oday; Krauss, Joachim K.; Hermann, Elvis J.

2024 Child s Nervous System

doi:10.1007/s00381-024-06367-y pmid:38557894

PurposePlacement of an external ventricular drainage (EVD) is one of the most frequent procedures in neurosurgery, but it has specific challenges and risks in the pediatric population. We here investigate the indications, management, and shunt conversion rates of an EVD.MethodsWe retrospectively...
LitStream

Journal Article

Clinical factors, management, and outcomes of children under 3years old with central nervous system tumors: single-center experience

Eker, Nurşah; Tokuç, Gülnur; Sarısaltık, Alican; Dağçınar, Adnan; Gül, Dilek; Atasoy, Beste Melek; Yılmaz, Barış; Taş, Burcu Tufan

2024 Child s Nervous System

doi:10.1007/s00381-024-06386-9 pmid:38619586

PurposeChildren under 3 years old represent a notable portion, about 25 to 30%, of all central nervous system tumor (CNS) cases. Their clinical course, prognosis, and treatment significantly differ from older children. This single-center retrospective study aims to comprehensively analyze...
LitStream

Journal Article

Giant cerebral cavernous malformation in a newborn: a rare case report and review of literature

Moreno, Ismael; Scalia, Gianluca; Umana, Giuseppe Emmanuele; Soriano, Ciro; Alcivar, Isis; Chaurasia, Bipin

2024 Child s Nervous System

doi:10.1007/s00381-024-06401-z pmid:38607549

BackgroundCavernous malformations (CMs), also known as cavernomas or cavernous angiomas, are vascular malformations characterized by sinusoidal spaces lined by endothelial cells. Giant CMs (GCMs) are extremely rare, with limited understanding of their presentation and management. We present a...

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