Results 211 to 220 of about 27,612 (251)
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Clinical Radiology, 1990
Acquired cholesteatoma of the middle ear is usually diagnosed by otoscopy and treated by exploratory surgery. The role of imaging for such cases is as controversial now as it was 10 years ago, despite significant improvements in spatial and contrast resolution resulting from computerised sectional imaging.
P D, Phelps, A, Wright
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Acquired cholesteatoma of the middle ear is usually diagnosed by otoscopy and treated by exploratory surgery. The role of imaging for such cases is as controversial now as it was 10 years ago, despite significant improvements in spatial and contrast resolution resulting from computerised sectional imaging.
P D, Phelps, A, Wright
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Biochemical and Biophysical Research Communications - BBRC, 2020
The occurrence and development of osteoclasts can directly affect the severity of bone destruction in middle ear cholesteatoma. At the same time, cell communication between keratinocytes and fibroblasts can stimulate osteoclast differentiation.
Ningyue Gong +7 more
semanticscholar +1 more source
The occurrence and development of osteoclasts can directly affect the severity of bone destruction in middle ear cholesteatoma. At the same time, cell communication between keratinocytes and fibroblasts can stimulate osteoclast differentiation.
Ningyue Gong +7 more
semanticscholar +1 more source
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
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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
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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
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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
The Endoscopic Management of Congenital Cholesteatoma.
Otolaryngologic clinics of North America, 2020Congenital cholesteatoma is a rare, primarily pediatric disease that presents in otherwise healthy ears. Typically, this disease is found in a well-defined sac in the middle ear, making it particularly suited for removal through transcanal endoscopic ear
R. McCabe, Daniel J. Lee, M. Fina
semanticscholar +1 more source
Predicting Recidivism for Acquired Cholesteatoma: Evaluation of a Current Staging System
Otology and Neurotology, 2020Objective: Assess the utility and prognostic capabilities of the European Academy of Otology and Neurotology (EAONO) and Japanese Otological Society (JOS) cholesteatoma classification system, specifically for retraction pocket cholesteatoma. Study Design:
S. Angeli +3 more
semanticscholar +1 more source
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
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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
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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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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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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
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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
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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
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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