Results 141 to 150 of about 7,140 (180)
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Cholesteatoma in children

The Laryngoscope, 1981
AbstractThe surgical management of cholesteatoma in children reMayns a controversial subject. Many authors hold that the disease itself is more aggressive than that seen in adults. Furthermore, there appears to be a consensus that intact canal wall procedures, if used at all, should be reserved for adults only.
M E, Glasscock, J R, Dickins, R, Wiet
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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
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CHOLESTEATOMA IN CHILDREN

Pediatric Clinics of North America, 1996
Cholesteatoma in children falls into two main categories: congenital and acquired. Though they present in different ways, both are potentially destructive lesions that are managed surgically. The goals of treatment are to eradicate keratinizing squamous epithelium from the temporal bone and to preserve or restore hearing.
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Evaluation of Cholesteatoma

Otolaryngologic Clinics of North America
Evaluation of cholesteatoma depends on clinical history and examination, with microscope and/or endoscope. A history of hearing loss with a chronic draining ear, refractory to ototopical medication, raises suspicion for cholesteatoma. Symptoms of Eustachian tube dysfunction or prior ear surgery including ear tubes should be elicited.
Anne K. Maxwell, Stephen R. Hoff
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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
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Biology of Cholesteatoma

Otolaryngologic Clinics of North America, 1989
Acquired cholesteatoma is a disease of the posterior superior part of the middle ear cleft that may arise from the external epithelium of the tympanic membrane. Three distinct epithelial zones of differing thicknesses characterize the development of this latter epithelium, and the thickness differences and their distribution in the eardrum and deep ...
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A Cholesteatoma Chronicle

Archives of Otolaryngology - Head and Neck Surgery, 1973
The special kind of keratoma found in the temporal bone, which has been called cholesteatoma by our otologic forefathers, was an unsolved problem in Virchow's time. It still is. I feel that a careful scrutiny of some classic words concerning cholesteatoma is in order.
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Congenital cholesteatoma

Otolaryngology–Head and Neck Surgery, 1993
R A, Clevens, B J, Wiatrak
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Intraspinal Cholesteatoma

Journal of Neuroscience Nursing, 1981
R P, Donnelly, C R, Greer, O H, Vreeland
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Cholesteatoma

Journal of the American Academy of Nurse Practitioners, 1990
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