Results 61 to 70 of about 317,091 (201)
Cholesteatoma of external auditory canal: a case report
PAMJ Clinical Medicine, 2019 Cholesteatoma is a common occurrence in the middle ear. Cholesteatoma of the external auditory canal (EAC) is a rare entity. We report the first case of our department of cholesteatoma of the EAC limited to the posterior wall, in a 14-year-old patient ...
Abdou Sy +3 more
doaj +1 more source
SVU - International Journal of Medical Sciences, 2022 Background: The use of diffusion-weighted (DW) sequences to distinguish recurrent cholesteatoma from chronic otitis media with granulations has shown to be quite effective.
Emad Edeen Ali* +3 more
doaj +1 more source
Short‐Term Complications Are Rare After Cholesteatoma Surgery
Clinical Otolaryngology, Volume 51, Issue 5, Page 660-665, September 2026.ABSTRACT Objective To evaluate the incidence and nature of short‐term complications following cholesteatoma surgery in a heterogeneous cohort. Design A retrospective cohort study including complete coverage of cholesteatoma surgery in a Swedish region between 1 January 2005 and 31 December 2015.
Agnes Modée Borgström +3 more
wiley +1 more source
Laryngoscope Investigative Otolaryngology, Volume 11, Issue 4, August 2026.ABSTRACT Introduction Chronic rhinosinusitis (CRS) and Eustachian tube dysfunction (ETD) frequently coexist, yet objective data quantifying their relationship remain scarce. Because both conditions can reflect shared mucosal inflammation, we investigated whether adults with objectively verified ETD harbor a larger paranasal sinus inflammatory burden on
Dachan Kim +2 more
wiley +1 more source
B-ENT, 2023 Cholesteatoma in the maxillary sinus is a rare disease entity and there is not much experience in treating this disease which often leads to recur. Here we report 2 cases of maxillary sinus cholesteatoma and explore its clinical features and surgical ...
Hongtao Zhen, Liyan Peng, Di Niu
doaj +2 more sources
Pediatric Pulmonology, Volume 61, Issue 8, August 2026.ABSTRACT Background Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder, and despite advances in next‐generation sequencing, a substantial proportion of clinically suspected pediatric cases remain without a molecular diagnosis.
Tilbe Hakçıl Öz +4 more
wiley +1 more source
Primary Ciliary Dyskinesia: A Suggested Pathway to Transition From Pediatric to Adult Care
Pediatric Pulmonology, Volume 61, Issue 8, August 2026.ABSTRACT Primary ciliary dyskinesia (PCD) is a rare, genetically heterogeneous disorder characterized by motile ciliary dysfunction that impairs mucociliary clearance. Symptoms of PCD can include unexplained neonatal respiratory issues, chronic sino‐otopulmonary symptoms, recurrent infections, bronchiectasis, and subfertility.
Abel De Castro +5 more
wiley +1 more source
Recurrence of cholesteatoma - A retrospective study including 1,006 patients for more than 33 years [PDF]
, 2020 Introduction Cholesteatomas are benign tumors consisting of skin, and growing inside a retraction pocket in the tympanic membrane. Cholesteatomas can occupy the entirety of the middle ear, and are known for their osteolytic capabilities.
Djurhuus, Bjarki D. +4 more
core +1 more source
World Journal of Otorhinolaryngology - Head and Neck Surgery, Volume 12, Issue 4, Page 442-452, August 2026.ABSTRACT Objectives Acquired cholesteatoma is an abnormal and invasive growth of keratinized squamous epithelial cells in the middle ear. The study aims to explore the role of exosomal miRNAs in the pathogenesis of acquired cholesteatoma and their potential in clinical application.
Qi Tang +12 more
wiley +1 more source
Medical Journal of Australia, Volume 224, Issue 8, August 2026.ABSTRACT Objective Determine whether watchful waiting is non‐inferior to immediate oral antibiotics for uncomplicated acute otitis media among urban Aboriginal and Torres Strait Islander children. Study Type Non‐inferiority unblinded randomised controlled trial.
Jennifer S. Reath +14 more
wiley +1 more source