Aug 2026· Medicina· Vol 86 Suppl 3, pp.
97-103
· 0 citations
Medicine
TL;DR
Bilateral leptomeningeal angioma and calcifications were associated with a more severe clinical phenotype, characterized by earlier seizure onset, higher rates of drug resistance, and cognitive impairment.
Background Sturge–Weber syndrome (SWS) is a rare congenital neurocutaneous disorder. Timely diagnosis and management remain challenging, particularly when intracranial hemorrhage (IH) occurs as a rare but serious complication. Case presentation A young child developed IH after minor head trauma and presented with irrit...
Yan-Mei Li, Jing Gan, Fan Ma et al.· Frontiers in Pediatrics· 0 citations
Abstract. Kimmerle anomaly (KA) is one of the most common osseous anomalies of the craniovertebral junction and may lead to vertebrobasilar insufficiency and neurovascular complications. The aim of this study was to analyze the incidence of KA in a neurological hospital, to identify the main clinical syndromes...
Re demonstrated heterogeneous electroclinical and neuroradiological evolution across pediatric and adult patients, and the coexistence of an older age profile and a predominance of left hemisphere involvement may suggest age-related phenotypic variability.
Ülkühan Öztoprak, C. Günbey, Rahşan Göçmen et al.· Brain & development (Tokyo....· 0 citations
BACKGROUND
Idiopathic syringomyelia (IS) in adults is rare, and its clinical course remains poorly defined. This study aimed to describe the clinical and radiological course of adult IS and to assess the relationship between imaging change and clinical outcome.
METHODS
Retrospective single-center study (2010-2025) in...
David Masson, Camille Nadler, I. Stella et al.· World Neurosurgery· 0 citations
Hypophysitis in sarcoidosis is a rare manifestation of neurosarcoidosis that may cause permanent endocrine dysfunction, visual impairment, and neurological morbidity. We performed a systematic review to characterize its clinical presentation, diagnostic findings, treatment, and outcomes. PubMed, Embase, and Scopus were...
Julia F B Cavalcanti, S. C. de Souza, L T Lucato et al.· Pituitary· 1 citation
Sturge-Weber syndrome (SWS), also called encephalotrigeminal angiomatosis, is a neurocutaneous disorder with angiomas that involve the leptomeninges and the skin of the face. It is a rare congenital non-hereditary disorder with incidence of 1: 20,000 – 50,000. Both sexes are affected equally. Presentation is usually in...
Gele Ih, A. M., Umar Fk et al.· EAS Journal of Radiology and...· 0 citations
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