Results 51 to 60 of about 1,323 (194)

Resolution of Pulmonary Inflammation and Obstruction Following Repair of Cerebrospinal Fluid Leak: A Case Report and Review of the Literature

open access: yesCase Reports in Pulmonology, Volume 2026, Issue 1, 2026.
Objectives Cerebrospinal fluid (CSF) rhinorrhea involves drainage of CSF through the nasal cavity due to disruption of the skull base, and pneumonitis secondary to CSF aspiration is a lesser‐known complication reported. We present the case of a patient whose pulmonary symptoms and function improved after surgical CSF leak repair. Methods This is a case
Ann O. Birmingham   +4 more
wiley   +1 more source

Poland Anomaly and Atretic Cephalocele in the Same Child: Coincidence or Association?

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.
ABSTRACT Poland Anomaly is a rare congenital disorder typically characterized by hypoplasia or agenesis of pectoral muscle with or without ipsilateral limb hypoplasia. The association of central nervous system malformation with Poland Anomaly has been rarely reported and includes craniofacial dysplasia, microcephaly, and Dandy‐Walker malformation ...
Alessandra Greta Grassi   +5 more
wiley   +1 more source

Congenital Giant Occipital Meningoencephalocele in A Holstein Calf Fetus

open access: yes, 2013
A 6-month-old dead fetus, removed from the uterus of a 4-year-old Holstein cow, was referred to our department. A fluctuant sac, approximately 25x20x30 cm, covered with skin was observed over the occipital region of the cranium.
Yaman, Duygu   +2 more
core   +1 more source

Transnasal Endoscopic Repair of Posttraumatic Meningoencephalocele: A Rare Presentation

open access: yesIndian Journal of Neurosurgery
Meningoencephalocele is a rare condition that results due to defect in skull base causing brain tissue to herniate along with meninges. We present a case of posttraumatic meningoencephalocele in an 11-year-old child, who presented with nasal mass and ...
Eshaan Kaushik   +3 more
doaj   +1 more source

Novel Compound Heterozygous Variants in the TCTN2 Gene Causing Meckel–Gruber Syndrome 8 in a Non‐Consanguineous Chinese Family

open access: yesMolecular Genetics &Genomic Medicine, Volume 13, Issue 12, December 2025.
Genetic analysis of the fetus with Meckel–Gruber syndrome 8 and the spectrum of TCTN2 variants. ABSTRACT Introduction Meckel‐Gruber syndrome (MKS, OMIM 24,900), also known as Meckel syndrome, is a rare and severe autosomal recessive disorder. The syndrome is typically characterized by a triad of occipital encephalocele, bilateral renal cystic dysplasia,
Qi Yang   +8 more
wiley   +1 more source

Iatrogenic meningoencephalocele after traumatic perforation of the cribriform plate during nasal intubation of a preterm infant

open access: yes, 2019
Traumatic iatrogenic meningoencephaloceles infants are rare and there is no consensus on management in the literature. This article presents a case of a meningoencephalocele diagnosed 15 months after a traumatic perforation of the cribriform plate due to
Dillenseger, L.   +7 more
core   +1 more source

Encephalocele within the Lateral Wall of the Sphenoid Sinus Presenting with Recurrent Meningitis and Cerebrospinal Fluid Rhinorrhea Repaired via Endoscopic Transnasal Transpterygoid Approach

open access: yesIndian Journal of Neurosurgery
The sphenoid sinus is an uncommon site for an encephalocele. It usually presents with cerebrospinal fluid (CSF) leak through the nasal cavity. Sternberg's canal (SC), which is a weak spot on the skull base, is one of the causes of spontaneous CSF leak ...
Dipuo Masege, John Ouma
doaj   +1 more source

Variations in Lateral Sphenoid Sinus Wall Defects

open access: yesIndian Journal of Neurosurgery, 2015
Objective The article aims to present different forms of lateral sphenoid sinus wall defects. Study Design Case series and literature review.
Gabriel Nakache   +2 more
doaj   +1 more source

[Meningoencephalocele].

open access: yesTidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke, 1991
A total of 52 children with meningoencephalocele were operated during a 23 year period. The anomaly was located frontally in nine children, occipitally in 34 children and infratentorially in nine children. Because of progressive hydrocephalus, 18 children underwent shunt procedures shortly after the initial surgical correction.
T, Lundar, H, Nornes
openaire   +1 more source

Expert Strategies: Skull Base Reconstruction—Global Perspectives, Insights, and Algorithms through a Mixed Methods Approach

open access: yesInternational Forum of Allergy &Rhinology, Volume 15, Issue 10, Page 1032-1069, October 2025.
ABSTRACT Objective There is limited consensus on endoscopic skull base surgery (ESBS) reconstruction principles. This study aims to generate comprehensive themes regarding ESBS reconstruction by pooling the experiences of ESBS experts, with comparison to a literature review of current published evidence.
Edward C. Kuan   +77 more
wiley   +1 more source

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