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Ear canal osteoma
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Ear canal osteoma

Contributors: Madeleine Strohl MD, Paul C. Bryson MD, MBA
Other Resources UpToDate PubMed

Synopsis

Ear canal osteomas are slow-growing, benign tumors that can develop in the bony external auditory canal.

Osteomas are uncommon. The incidence is estimated to be less than 0.5%. The literature suggests that ear canal osteomas can affect a wide range of age groups starting in the second decade of life. It is estimated that it is more common in males. No clear etiology or risk factors have been linked to their development. These are distinct from exostoses, which have frequent cold water exposure as a risk factor.

The growths are typically asymptomatic unless they are obstructive. On most occasions, they are discovered accidentally during an otoscopic or radiographic exam. If the outgrowth obstructs the ear canal, patients can complain of ear pain, hearing loss, or recurrent outer ear infections. On physical exam, one will see a pearly white, bony outgrowth at the bony-cartilaginous junction in the external ear canal.

Prognosis is excellent. Treatment with surgical excision is only necessary if the patient is symptomatic.

Codes

ICD10CM:
H61.819 – Exostosis of external canal, unspecified ear

SNOMEDCT:
277417007 – External auditory canal osteoma

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Last Updated:10/27/2015
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Ear canal osteoma
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A medical illustration showing key findings of Ear canal osteoma : Hearing loss, Tumor, Unilateral distribution, Otalgia
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