Results 41 to 50 of about 25,873,689 (163)

Lymphangioma‐Induced Macroglossia in an Adolescent: A Case Report

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Lymphangioma is a congenital malformation of the lymphatic system, commonly affecting the head and neck region. Macroglossia due to lymphangioma in adolescence is uncommon, making this case noteworthy. This condition can affect oral function, speech, and quality of life, making early diagnosis and intervention essential. This report highlights
Arezoo Heidary, Mojtaba Mehrabanian
wiley   +1 more source

Glucocorticoid‐Induced Tumor Necrosis Factor Receptor Ligand: Correlation and Therapeutic Potential for Cognitive Impairment in Temporal Lobe Epilepsy

Clinical and Translational Science, Volume 19, Issue 2, February 2026.
ABSTRACT Immune checkpoint regulators can improve neurological functions in Alzheimer's disease. However, it remains blurred whether these regulators may ameliorate temporal lobe epilepsy (TLE) and TLE‐related cognitive impairment. This study analyzed the bulk transcriptomic data of human TLE hippocampi by bioinformatics.
Man Li, Jinying Shi, Xiaodong Pan, Huapin Huang   +3 more
wiley   +1 more source

Clinical study on CyberKnife for treating giant cavernous hemangioma in cavernous sinus region

Chinese Journal of Contemporary Neurology and Neurosurgery, 2015
Objective To investigate the efficacy and safety of CyberKnife for giant cavernous hemangioma in cavernous sinus. Methods The data of 7 cases of giant cavernous hemangioma in cavernous sinus region confirmed by imaging examination and treated with ...
Lu SUN, Long-sheng PAN, Wei-jun WANG, Jin-yuan WANG, Zhi-zhong ZHANG, Zhong-jian JU, Zhi-pei LING, Bao-lin QU, Xin-guang YU   +8 more
doaj  

Cerebrovascular Malformations Associated With Hereditary Hemorrhagic Telangiectasia and HHT‐Like Syndromes: A Comparative Overview

European Journal of Neurology, Volume 33, Issue 2, February 2026.
Hereditary hemorrhagic telangiectasia (HHT) and several HHT‐like syndromes, including Wyburn–Mason, Cobb, Klippel–Trénaunay, Parkes Weber, neurofibromatosis type 1, PHACE(S), capillary malformation–AVM (CM‐AVM), Juvenile polyposis/HHT overlap, HHT type 5, PTEN hamartoma tumor syndrome, and blue rubber bleb nevus syndrome, share overlapping ...
Matteo Palermo, Carmelo Lucio Sturiale
wiley   +1 more source

Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss families [PDF]

, 2010
Cavernous malformations (CCMs) are benign, well-circumscribed, and mulberry-like vascular malformations that may be found in the central nervous system in up to 0.5% of the population. Cavernous malformations can be sporadic or inherited.
Graeni, C, Bonassin, F, Siegel, A M, Sturzenegger, M, Stepper, F, Baumgartner, R W, Andermann, F, Rouleau, G A, Georgiadis, D, Merlo, A, Verlaan, D J, Baumann, C R, Verlaan DJ, Georgiadis D, Siegel AM, Merlo A, Baumgartner RW, Graeni C, Stepper F, Baumann CR, Bonassin F, Rouleau GA, Andermann F, Sturzenegger M   +23 more
core   +2 more sources

Clinical study of intercellular adhesion molecule⁃1 expression in endothelial⁃derived exosome in children with intracranial cavernous hemangioma with epilepsy

Chinese Journal of Contemporary Neurology and Neurosurgery, 2020
Objective To investigate the expression and mechanism of exosomal intercellular adhesion molecule ⁃ 1 (ICAM ⁃ 1) in patients with intracranial cavernous hemangioma (CCM) associated epilepsy.
Bin LI, Hui ZHOU, Ai⁃qin JIN
doaj  

Familial Cerebral Cavernous Malformations: Pathophysiology, Genetics, Biomarkers, and Treatment Perspectives

Journal of Neurochemistry, Volume 170, Issue 1, January 2026.
Cerebral cavernous malformations (CCMs) are vascular lesions in the brain caused by inherited genetic mutations in the CCM1/2/3 genes that disrupt normal blood vessel function. This work demonstrates that these mutations lead to endothelial dysfunction, inflammation, and iron accumulation, which can be detected by magnetic resonance imaging (MRI) and ...
Fabrícia Lima Fontes‐Dantas, Gustavo da Fontoura Galvão, Alexandre Martins Cunha, Pedro de Sena Murteira Pinheiro, Verônica Morandi, Jorge Marcondes de Souza   +5 more
wiley   +1 more source

Lumbo‐sacral cavernous hemangioma : a rare case [PDF]

, 2016
Pure spinal epidural cavernous angiomas are very rare, with only less than 100 cases on literature review. The average age of onset is 51 years, and it is more common in women than in men. Lumbo‐sacral spine is involved in less than 10% of reported cases.
EL ABBADI, N., BOUCHAOUCH, A.
core  

A Schwannoma in the Anterior Orbit: Case Report and Literature Review

Case Reports in Ophthalmological Medicine, Volume 2026, Issue 1, 2026.
Introduction Orbital schwannoma is a rare tumor that can occur in any orbital compartment, posing a diagnostic challenge for clinicians. Case Presentation We report a 35‐year‐old male who presented with a visible schwannoma in the inferomedial orbital angle. Our patient was treated with en bloc transconjunctival surgical resection without complications.
Bassam Alobaid, Rahaf Alok, Karuna Sharma   +2 more
wiley   +1 more source

A Case of Cavernous Hemangioma Detected in Adulthood

, 2013
Benign vascular tumors are rarely seen in the mediastinum and mediastinal hemangioma is the most common one among them. However, its prevalence is less than 0.5% among all mediastinal tumors.
Şule Bakır, Erkan Akar, Taşkın Erkinüresin   +2 more
core   +1 more source