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Notes
- 1.
Exostosis: A cartilage-capped bony projection arising from any bone that develops from cartilage. Stedman’s Electronic Medical Dictionary.
- 2.
Cholesteatoma: Squamous metaplasia or extension of squamous cell epithelium inward to line an expanding cystic cavity that may involve the middle ear or mastoid, erode surrounding bone, and become filled with a mass of keratinized squamous cell epithelial debris, usually resulting from chronic otitis media. The lesion often contains cholesterol clefts surrounded by inflammatory and foreign body giant cells, hence the name cholesteatoma. Stedman’s Electronic Medical Dictionary.
- 3.
Wegener’s granulomatosis: a disease, occurring mainly in the fourth and fifth decades, characterized by necrotizing granulomas and ulceration of the upper respiratory tract, with purulent rhinorrhea, nasal obstruction, and sometimes with otorrhea, hemoptysis, pulmonary infiltration and cavitation, and fever; exophthalmos, involvement of the larynx and pharynx, and glomerulonephritis may occur; the underlying condition is a vasculitis affecting small vessels, and is possibly due to an immune disorder. Stedman’s Online Medical Dictionary.
- 4.
Langerhans cell histiocytosis: a set of closely related disorders unified by a common proliferating element, the Langerhans cell. Three overlapping clinical syndromes are recognized: a single site disease (eosinophilic granuloma), a multifocal unisystem process (Hand-Schuller-Christian syndrome), and a multifocal, multisystem histiocytosis (Letter-Siwe syndrome.) Formerly this process was known as histiocytosis X. Stedman’s Online Medical Dictionary.
- 5.
Sarcoidosis: a systemic granulomatous disease of unknown cause, especially involving the lungs with resulting interstitial fibrosis, but also involving lymph nodes, skin, liver, spleen, eyes, phalangeal bones, and parotid glands; granulomas are composed of epithelioid and multinucleated giant cells with little or no necrosis. Stedman’s Online Medical Dictionary.
- 6.
Mondini dysplasia: Congenital anomaly of osseus and membranous otic labyrinth characterized by aplastic cochlea and deformity of the vestibule and semicircular canals with partial or complete loss of auditory and vestibular function; may be associated with dilated vestibular aqueduct and spontaneous cerebrospinal fluid otorrhea resulting in meningitis.
- 7.
Scheibe dysplasia: Hearing impairment due to cochleosaccular dysplasia; usually autosomal recessive inheritance. Stedman’s Online Medical Dictionary.
- 8.
Cogan syndrome: Typical Cogan syndrome is characterized by interstitial keratitis and vestibuloauditory dysfunction. There is generally a brief episode of inflammatory eye disease (interstitial keratitis) followed by bilateral audiovestibular symptoms. The interstitial keratitis usually occurs with sudden onset and is characterized by photophobia, lacrimation, and eye pain. The vestibuloauditory dysfunction is usually bilateral, presenting with tinnitus, sensorineural hearing loss, and acute episodes of vertigo.
- 9.
Relapsing polychondritis: a degenerative disease of cartilage producing a bizarre form of arthritis, with collapse of the ears, the cartilaginous portion of the nose, and the tracheobronchial tree; death may occur from chronic infection or suffocation because of loss of stability in the tracheobronchial tree; of autosomal origin. Stedman’s Online Medical Dictionary.
Abbreviations
- AIED:
-
Autoimmune inner ear disease
- NSHL:
-
Non-syndromic hearing loss
- SHL:
-
Syndromic hearing loss
References
Takemori S, Tanaka Y, Suzuki JI. Thalidomide anomalies of the ear. Arch Otolaryngol, 1976;102(7):425–7
Ostrowski VB, Wiet RJ. Pathologic conditions of the external ear and auditory canal. Postgrad Med, 1996;100(3):223–8, 233–7
Adams WS. The aetiology of swimmer’s exostoses of the external auditory canals and of associated changes in hearing. J Laryngol Otol, 1951;65(4):232–50; concl.
Mlynski R, Radeloff A, Brunner K, Hagen R. [Exostoses of the external auditory canal Is the cold water hypothesis valid for patients in continental areas?] HNO, 2008;56(4):410–6. German
Van Gilse, PHG. Des observations ultérieures sur la genèse des exostoses du conduit externe par l’irritation d’eau froide. Acta Otolaryngol, 1938;2:343–352
Breau RL, Gardner EK, Dornhoffer JL. Cancer of the external auditory canal and temporal bone. Curr Oncol Rep, 2002;4(1):76–80
Horbelt CV. A review of physical, behavioral, and oral characteristics associated with Treacher Collins syndrome, Goldenhar syndrome, and Angelman syndrome. Gen Dent, 2008;56(5):416–9
Rice DP. Clinical features of syndromic craniosynostosis. Front Oral Biol, 2008;12:91–106
Jahrsdoerfer RA, Yeakley JW, Aguilar EA, Cole RR, Gray LC. Grading system for the selection of patients with congenital aural atresia. Am J Otol, 1992;13(1):6–12
Timmermans K, Vander Poorten V, Desloovere C, Debruyne F. The middle ear of cleft palate patients in their early teens: a literature study and preliminary file study. B-ENT, 2006;2(Suppl 4):95–101
Phua YS, Salkeld LJ, de Chalain TM. Middle ear disease in children with cleft palate: protocols for management. Int J Pediatr Otorhinolaryngol, 2009;73(2):307–13
Chole RA, McKenna M. Pathophysiology of otosclerosis. Otol Neurotol, 2001;22(2):249–57
Altmann F, Glasgold A, Macduff JP. The incidence of otosclerosis as related to race and sex. Ann Otol Rhinol Laryngol, 1967;76(2):377–92
Markou K, Goudakos J. An overview of the etiology of otosclerosis. Eur Arch Otorhinolaryngol, 2009;266(1):25–35
Ali IBH, Thys M, Beltaief N, Schrauwen I, Hilgert N, Vanderstraeten K, Dieltjens N, Mnif E, Hachicha S, Besbes G, Arab SB, Van Camp G. A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9. Hum Genet, 2008;123(3):267–72
Niedermeyer HP, et al., Measles virus and otosclerosis. Adv Otorhinolaryngol, 2007;65:86–92
Lippy WH, Berenholz LP, Schuring AG, Burkey JM. Does pregnancy affect otosclerosis? Laryngoscope, 2005;115(10):1833–6
Dahlqvist A, Diamant H, Dahlqvist SR, Cedergren B. HLA antigens in patients with otosclerosis. Acta Otolaryngol, 1985;100(1–2):33–5
Gristwood RE, Venables WN. Otosclerosis and chronic tinnitus. Ann Otol Rhinol Laryngol, 2003;112(5):398–403
Sobrinho PG, Oliveira CA, Venosa AR. Long-term follow-up of tinnitus in patients with otosclerosis after stapes surgery. Int Tinnitus J, 2004;10(2):197–201
Sellari-Franceschini S, Ravecca F, De Vito A, Berrettini S. [Progressive sensorineural hearing loss in cochlear otosclerosis]. Acta Otorhinolaryngol Ital, 1998;18(4 Suppl 59):59–65
Shinkawa A, Sakai M, Ishida K. Cochlear otosclerosis 30 years after stapedectomy confirmed by CT, MRI. Auris Nasus Larynx, 1998;25(1):95–9
Linthicum F, Jr. Post-stapedectomy cochlear otosclerosis. Ear Nose Throat J, 2009;88(4):872
Hinojosa R, Marion M. Otosclerosis and sensorineural hearing loss: a histopathologic study. Am J Otolaryngol, 1987;8(5):296–307
Ramsden R, Rotteveel L, Proops D, Saeed S, van Olphen A, Mylanus E. Cochlear implantation in otosclerotic deafness. Adv Otorhinolaryngol, 2007;65:328–34
Mafee MF. Use of CT in the evaluation of cochlear otosclerosis use of CT in the evaluation of cochlear otosclerosis. Radiology, 1985;156(3):703–8
Alford BR, Guilford FR. A comprehensive study of tumors of the glomus jugulare. Laryngoscope, 1962;72:765–805
Gulya AJ. The glomus tumor and its biology. Laryngoscope, 1993;103(11 Pt 2 Suppl 60):7–15
Horn KL, Hankinson H. (1994) Tumors of the jugular foramen, in Neurotology, RK Jackler, DE Brackmann, Editors, Mosby: New York, 1059–64
Sismanis A. (1997) Pulsatile tinnitus, in Clinical otology, GB Hughes, ML Pensak, Editors, Thieme: New York, 445–60
Wackym PA, Friedman I. (2000) Unusal tumors of the middle ear and mastoid, in Tumors of the ear and temporal bone, RK Jackler, CLW Driscoll, Editors, Lippincott Williams & Wilkins: Philadelphia, 128–45
Birkenhager R, Aschendorff A, Schipper J, Laszig R. [Non-syndromic hereditary hearing impairment]. Laryngorhi nootologie, 2007;86(4):299–309; quiz 310–3
Kitamura K, Takahashi K, Tamagawa Y, Noguchi Y, Kuroishikawa Y, Ishikawa K, Hagiwara H. Deafness genes. J Med Dent Sci, 2000;47(1):1–11
Bayazit YA, Yilmaz M. An overview of hereditary hearing loss. ORL J Otorhinolaryngol Relat Spec, 2006;68(2):57–63
Smith RJ, Bale JF, Jr, White KR. Sensorineural hearing loss in children. Lancet, 2005;365(9462):879–90
Hess C, Rosanowski F, Eysholdt U, Schuster M. [Hearing impairment in children and adolescents with Down’s syndrome]. HNO, 2006;54(3):227–32
Batissoco AC, Abreu-Silva RS, Braga MC, Lezirovitz K, Della-Rosa V, Alfredo T, Jr, Otto PA, Mingroni-Netto RC. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 Brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling. Ear Hear, 2009;30(1):1–7
Douglas SA, Sanli H, Gibson WP. Meningitis resulting in hearing loss and labyrinthitis ossificans – does the causative organism matter? Cochlear Implants Int, 2008;9(2):90–6
Hviid A, Rubin S, Muhlemann K. Mumps. Lancet, 2008;371(9616):932–44
Sweeney CJ, Gilden DH. Ramsay Hunt syndrome. J Neurol Neurosurg Psychiatry, 2001;71(2):149–54
Sugiura M, Naganawa S, Nakata S, Kojima S, Nakashima T. 3D-FLAIR MRI findings in a patient with Ramsay Hunt syndrome. Acta Otolaryngol, 2007;127(5):547–9
McCabe BF. Autoimmune sensorineural hearing loss. Ann Otol Rhinol Laryngol, 1979;88(5 Pt 1):585–9
Ruckenstein MJ. Autoimmune inner ear disease. Curr Opin Otolaryngol Head Neck Surg, 2004;12(5):426–30
Broughton SS, Meyerhoff WE, Cohen SB. Immune-mediated inner ear disease: 10-year experience. Semin Arthritis Rheum, 2004;34(2):544–8
Bovo R, Ciorba A, Martini A. The diagnosis of autoimmune inner ear disease: evidence and critical pitfalls. Eur Arch Otorhinolaryngol, 2009;266(1):37–40
Cruickshanks KJ, Wiley TL, Tweed TS, Klein BE, Klein R, Mares-Perlman JA, Nondahl DM. Prevalence of hearing loss in older adults in Beaver Dam, Wisconsin The Epidemiology of Hearing Loss Study. Am J Epidemiol, 1998;148(9):879–86
Mazurek B, Stöver T, Haupt H, Gross J, Szczepek A. [Pathogenesis and treatment of presbyacusis current status and future perspectives]. HNO, 2008;56(4):429–32; 434–5
Rosenhall U, Karlsson AK. Tinnitus in old age. Scand Audiol, 1991;20(3):165–71
Nondahl DM, Cruickshanks KJ, Wiley TL, Klein R, Klein BE, Tweed TS. Prevalence and 5-year incidence of tinnitus among older adults: the epidemiology of hearing loss study. J Am Acad Audiol, 2002;13(6):323–31
do Carmo LC, Médicis da Silveira JA, Marone SA, D’Ottaviano FG, Zagati LL, Dias von Söhsten Lins EM. Audiological study of an elderly Brazilian population. Braz J Otorhinolaryngol, 2008;74(3):342–9
Ahmad N, Seidman M. Tinnitus in the older adult: epidemiology, pathophysiology and treatment options. Drugs Aging, 2004;21(5):297–305
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Kleinjung, T. (2011). Conductive and Cochlear Hearing Loss. In: Møller, A.R., Langguth, B., De Ridder, D., Kleinjung, T. (eds) Textbook of Tinnitus. Springer, New York, NY. https://doi.org/10.1007/978-1-60761-145-5_34
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