Results 261 to 270 of about 33,888 (298)
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Lethal Cholesteatoma

Otolaryngology–Head and Neck Surgery, 1986
Aural cholesteatoma Is a disease entity well known to the otologic community. Complications of cholesteatoma, although uncommon, are not usually life threatening. We present two cases in which a unique and hitherto unreported pathway of spread of a cholesteatoma is noted.
R A, Jahrsdoerfer   +3 more
openaire   +2 more sources

Cholesteatoma

Otolaryngologic Clinics of North America
Abstract A patient with a cholesteatoma (active squamous chronic otitis media) classically presents with recurrent episodes of foul-smelling otorrhoea and hearing loss. Unrecognized and untreated, a cholesteatoma can progressively destroy structures within and around the temporal bone, resulting in lasting morbidity, and may ...
Samantha, Anne, Michael, Hoa
  +5 more sources

Congenital Cholesteatoma

Otolaryngologic Clinics of North America, 1978
Congenital cholesteatoma of the temporal bone may be encountered by the otologist in the cerebellopontine angle, petrous bone, or middle ear cleft; the latter occurrence seems most likely. The etiology, epidemiologic factors, location of intracranial occurrence, clinical features, methods of diagnosis, differential diagnosis, gross and microscopic ...
M M, Paparella, L, Rybak
openaire   +2 more sources

Cholesteatoma staging

The Laryngoscope, 1986
AbstractManuscripts reporting results of surgery for chronic otitis media would be more meaningful if standardized nomenclature were used in describing the type of surgery performed and if standardized classifications were used for the disease process. Standardized nomenclature for surgery type and classifications for chronic otitis media exist.
W L, Meyerhoff, J, Truelson
openaire   +2 more sources

Congenital Cholesteatoma

Otolaryngology - Head and Neck Surgery, 1994
AbstractSince the late 1970s, the author has had the opportunity to prospectively study, document, and surgically manage 40 cases of congenital cholesteatoma. All cases met strict criteria for inclusion in the study, all were surgically and pathologically confirmed, and were definitively followed. During that same period, 38 cases were managed by other
openaire   +4 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

Growth and Late Detection of Post-Operative Cholesteatoma on Long Term Follow-Up With Diffusion Weighted Magnetic Resonance Imaging (DWI MRI): A Retrospective Analysis From a Single UK Centre.

Otology and Neurotology, 2019
OBJECTIVE To evaluate the growth rate and late detection of residual cholesteatoma on long-term follow-up with diffusion weighted magnetic resonance imaging (DWI MRI) in clinically stable ears following definitive surgery, in order to define surveillance
I. Pai   +4 more
semanticscholar   +1 more source

Congenital cholesteatoma

The Journal of Laryngology & Otology, 1991
AbstractWe present a British series of eleven patients with primary cholesteatoma, including one patient with bilateral disease. Eight children presented with a history of hearing loss, while one child had had recurrent otitis media and another had had carache. Operative findings were: in five ears, cholesteatoma confined to the antero-superior segment
B, Laskiewicz   +4 more
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

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

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