Results 31 to 40 of about 2,979 (167)

Isolated Tuberculoma Mimicking Foramen Magnum Meningioma in the Absence of Primary Tuberculosis: A Case Report [PDF]

open access: yesNeurospine, 2018
Central nervous system tuberculosis is a devastating complication of systemic tuberculosis. Intradural extramedullary (IDEM) tuberculoma at the foramen magnum is rare, and mimics en plaque meningioma.
Manish Kolakshyapati   +6 more
doaj   +1 more source

Syringomyelia as a presenting feature of shunt dysfunction: Implications for the pathogenesis of syringomyelia

open access: yesJournal of Craniovertebral Junction and Spine, 2012
The pathogenesis of syringomyelia continues to be an enigma. The patency of the central canal and its role in the pathogenesis of communicating syringomyelia continues to elicit controversy.
Natarajan Muthukumar
doaj   +1 more source

Surgical Outcomes of C1-2 Posterior Stabilization in Patients With Chiari Malformation Type 1

open access: yesGlobal Spine Journal, 2022
Study Design: Retrospective chart review. Objectives: Chiari malformation (CM) is characterized by a downward displacement of the cerebellar tonsils through the foramen magnum.
Ali Arslan MD   +6 more
doaj   +1 more source

Comprehensive comparative study of Chiari-like malformation in veterinary and human medicine

open access: yesVeterinární Medicína
This review aims to enrich our understanding of Chiari-like malformation (CLM) by combining human and veterinary insights, and providing a detailed cross-species overview.
JH Jung, H Park, WS Kim, HY Yoon
doaj   +1 more source

Is Cervical Stabilization for All Cases of Chiari-I Malformation an Overkill? Evidence Speaks Louder Than Words! [PDF]

open access: yesNeurospine, 2019
Chiari I malformation is characterized by the downward displacement of cerebellar tonsils through the foramen magnum. While discussing the treatment options for Chiari I malformation, the points of focus include: (1) Has the well-established procedure of
Harsh Deora   +4 more
doaj   +1 more source

Pseudo Chiari with holocord syringomyelia secondary to cerebrospinal fluid hypotension. Case report

open access: yesInterdisciplinary Neurosurgery, 2022
Introduction: Pseudo-Chiari malformation results from caudal displacement of brain structures secondary to cerebrospinal fluid (CSF) hypotension. Some case reports in the syringomyelia literature are associated with a pseudo-Chiari malformation.
Emiliano Lorefice   +4 more
doaj   +1 more source

Outcomes of 87 small‐breed dogs surgically treated for Chiari‐like malformation and syringomyelia

open access: yesVeterinary Surgery, EarlyView.
Abstract Objective To report the outcomes of titanium mesh (TM) cranioplasty without polymethylmethacrylate (PMMA), incorporating a deliberate gap between the foramen magnum decompression (FMD) surface and the TM, in small‐breed dogs with Chiari‐like malformation and syringomyelia (CM/SM). Study design Retrospective clinical study.
Sung Su Park, Ji Young Park, Ho Jae Han
wiley   +1 more source

Homozygous Achondroplasia With Long‐Term Survival: Growth Patterns, Medical Interventions, and Practice Implications

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1372-1377, June 2026.
ABSTRACT Homozygous achondroplasia is widely considered perinatal lethal by the medical community. In this case series, we report two children from a single family with longer‐term survival. One child lived for 17 months and the other was 60 months at the time of publication.
Hannah Singerline   +3 more
wiley   +1 more source

Trapped Fourth Ventricle in a Pediatric Patient With a History of Post‐Traumatic Hydrocephalus and Ventriculoperitoneal Shunt: A Case Report and Literature Review

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Trapped fourth ventricle (TFV) is a rare, serious complication of ventriculoperitoneal (VP) shunting that can mimic posterior fossa tumors and cause life‐threatening brainstem compression. We report the case of a 7‐year‐old boy with a history of a VP shunt for post‐traumatic hydrocephalus who presented with progressive drowsiness and gait ...
Muhammad Hamza   +8 more
wiley   +1 more source

Genetic Bone Diseases: A Scoping Review of Pathology, Symptoms, Diagnosis, Treatment, and New Horizons

open access: yesAdvanced Genetics, Volume 7, Issue 2, June 2026.
This review highlights six genetic diseases of the bone, aiming to provide clinicians and researchers with updated information on their diagnosis and treatment. It also includes an assessment of common clinical and radiographic findings, along with pathophysiology related to diseases.
Colin Jones, Ambalangodage C. Jayasuriya
wiley   +1 more source

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