Results 221 to 230 of about 27,612 (251)
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Congenital Cholesteatoma

Archives of Otolaryngology - Head and Neck Surgery, 1995
To review the characteristics of congenital cholesteatomata.Case series.Tertiary care (referral-based) private practice.Fourteen patients were included in the study. The diagnosis of congenital cholesteatoma was based on an intact tympanic membrane on physical examination; a history that excluded tympanic membrane perforation, otorrhea, or previous ...
J J, Zappia, R J, Wiet
openaire   +2 more sources

Endoscopic Versus Microscopic Management of Attic Cholesteatoma: A Randomized Controlled Trial

The Laryngoscope, 2019
To compare endoscopic transcanal approach to attic cholesteatoma with conventional microscopic transcanal ...
Arindam Das   +3 more
semanticscholar   +1 more source

Congenital Cholesteatoma

Pediatric Annals, 2016
Congenital cholesteatoma is one of the more common causes of the onset of childhood conductive hearing loss unrelated to middle ear effusion. If undiagnosed, the disease can progress to irreversibly destroy the conductive hearing architecture, as well as the surrounding skull base of the lateral temporal bone.
David, Walker, Michael J, Shinners
openaire   +2 more sources

International Collaborative Assessment of the Validity of the EAONO-JOS Cholesteatoma Staging System.

Otology and Neurotology, 2019
OBJECTIVE Assessment of validity of the Japanese Otological Society and the European Academy of Otology and Neurotology (EAONO-JOS) cholesteatoma staging system (EJS) through international collaboration to investigate: (a) feasibility of retrospectively ...
A. James   +9 more
semanticscholar   +1 more source

Renal cholesteatoma

Urology, 1988
Renal cholesteatoma is being reported more frequently in the literature. A case with a twenty-year documented history is presented, together with observations on differential diagnosis.
R P, Molina, D A, Dulabon, R B, Roth
openaire   +2 more sources

Negative Predictive Value of Non-Echo-Planar Diffusion Weighted MR Imaging for the Detection of Residual Cholesteatoma Done at 9 Months After Primary Surgery Is not High Enough to Omit Second Look Surgery.

Otology and Neurotology, 2019
OBJECTIVES To evaluate non echo-planar diffusion weighted magnetic resonance imaging (non-EP DW MRI) at 9 months after primary surgery to rule out residual cholesteatoma in patients scheduled before second-look-surgical exploration.
R. J. Horn   +4 more
semanticscholar   +1 more source

Comparison of the EAONO/JOS, STAMCO and ChOLE cholesteatoma staging systems in the prognostic evaluation of acquired middle ear cholesteatoma in children

European Archives of Oto-Rhino-Laryngology, 2022
Xiaoxu Wang   +9 more
semanticscholar   +1 more source

Congenital Cholesteatoma

Otolaryngologic Clinics of North America
Congenital cholesteatoma is a cyst of keratinizing squamous cell epithelium in the setting of an intact tympanic membrane, in a patient without a history of otorrhea, tympanic membrane perforation, or otologic surgery. The most common presentation of a congenital cholesteatoma is that of an asymptomatic pearly white mass in the anterosuperior quadrant ...
openaire   +2 more sources

Long term outcomes of canal wall up and canal wall down tympanomastoidectomies in pediatric cholesteatoma.

International Journal of Pediatric Otorhinolaryngology, 2021
G. Piras   +6 more
semanticscholar   +1 more source

Microbiome Analysis of Cholesteatoma by Gene Sequencing.

Otology and Neurotology, 2019
OBJECTIVE To compare the microbial flora of cholesteatoma and normal middle ears using gene-based sequencing analysis. STUDY DESIGN Controlled ex vivo human study. SETTING Academic, tertiary medical center.
Joshua P. Weiss   +2 more
semanticscholar   +1 more source

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