Results 51 to 60 of about 8,831 (219)

Nuestra experiencia en el manejo quirúrgico de la mastoiditis aguda infantil

open access: yesRevista Portuguesa Otorrinolaringologia e Cirurgia de Cabeça e Pescoço, 2010
Objetivo: revisión de nuestra experiencia en el manejo quirúrgico de la mastoiditis aguda. Material y método: estudio retrospectivo de 23 pacientes (13 varones y 10 mujeres) menores de 15 años tratados quirúrgicamente de mastoiditis aguda entre enero ...
Ana Faraldo García   +5 more
doaj   +1 more source

Sigmoid and Transverse Sinus Thrombosis as a Complication of Chronic Suppurative Otitis Media in a Child: A Case Report and Review of Literature

open access: yesClinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT Chronic suppurative otitis media is an easily managed condition with potential for severe sinus thrombophlebitis complications secondary to cholesteatoma, if not diagnosed and treated promptly. Diagnosis relies on the culture and sensitivity of the drained suppuration, computed tomography (CT), and magnetic resonance imaging (MRI).
Abdullah Nadeem   +8 more
wiley   +1 more source

Pediatric Acute Mastoiditis in Saudi Arabia: Demographic Insights, Clinical Profiles, and Prognostic Factors

open access: yesChildren
Acute mastoiditis, a complication of otitis media, poses significant challenges in diagnosis and treatment, particularly in pediatric populations.
Sarah Alshehri, Khalid A. Alahmari
doaj   +1 more source

Lemierre syndrome presenting as acute mastoiditis in a 2-year-old girl with congenital dwarfism

open access: yesInfectious Disease Reports, 2015
Lemierre syndrome is defined by septic thrombophlebitis of the internal jugular vein caused by Fusobacterium. Historically, these infections originate from the oropharynx and typically are seen in older children, adolescents and young adults.
Jason B. Fischer   +3 more
doaj   +1 more source

Facial nerve schwannoma mimicking acute mastoiditis

open access: yesOtolaryngology Case Reports, 2021
Benign tumors of the temporal bone are extremely rare, with an incidence of 1 in 200,000 individuals. The authors report a case of an 8-year-old girl with facial nerve schwannoma (FNS) involving the mastoid portion of her facial nerve.
Kevin Wong   +5 more
doaj   +1 more source

The Global Burden of Cholesteatoma: A Systematic Review and Meta‐analysis

open access: yesOtolaryngology–Head and Neck Surgery, Volume 174, Issue 1, Page 45-56, January 2026.
Abstract Objective This systematic review and meta‐analysis sought to estimate the global and World Health Organization (WHO) regional prevalence and burden of cholesteatoma. Data Sources PubMed, APA PsycINFO, the Cochrane Library, Embase, and WHO International Clinical Trials Registry Platform (ICTRP) from 2010 to 2025.
Herbert Melariri   +21 more
wiley   +1 more source

From Sound to Silence: Cerebellar Abscesses and Herniation Due to Cochlear Implant Infection With Escherichia coli and Bacteroides fragilis

open access: yesCase Reports in Infectious Diseases, Volume 2026, Issue 1, 2026.
Cochlear implantation (CI) is a safe and well‐established intervention for sensorineural hearing loss, with a low incidence of severe postoperative infections. We present the first reported case of cerebellar abscess and herniation due to CI infection. This unique case involves a 57‐year‐old man with recurrent cochlear implant infections, necessitating
Celine Molfetta   +5 more
wiley   +1 more source

Acute coalescent mastoiditis in a 16-month-old child due to Streptococcus pneumoniae infection

open access: yesJournal of Acute Disease
Rationale: Acute otitis media is a common disease in early childhood, and is usually caused by Streptococcus pneumoniae (S. pneumoniae). Acute mastoiditis is a complication of acute otitis media and can involve not only the mucoperiosteum of the middle ...
Magdalena Pszczołowska   +4 more
doaj   +1 more source

Novel Nonsense Mutation in SMARCD2 Gene Results in Dysplasia of All Myeloid Cell Lines

open access: yeseJHaem, Volume 6, Issue 6, December 2025.
ABSTRACT Introduction Specific granule deficiency type II (SGD2) is a rare heterogeneous congenital disease characterized by early‐onset life‐threatening infections. SGD2 is caused by autosomal recessive mutations in the SMARCD2 gene. Methods Prenatal screening in our patient revealed a novel homozygous nonsense mutation in SMARCD2 (c.208C>T, p.Gln70*).
Michelle A. E. Brouwer   +6 more
wiley   +1 more source

Squamozygomatic mastoiditis

open access: yesBrazilian Journal of Otorhinolaryngology, 2008
Acute atypical mastoiditis, with temporal and/or facial edema, is called squamozygomatic mastoiditis. There are only a few reports of this occurrence in the literature, which occurs because of an inflammatory process spread to the zygommatic apophysis, when mastoid pneumatization reaches the zygoma or the squamous portion of the temporal bone ...
de Pinho Marques Araújo, Patrícia   +5 more
openaire   +2 more sources

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