Short answer · Medically reviewed summary · Last updated: 2026-04-08
The ICD-10 code for cholesteatoma of the middle ear is H71, which includes various sub-classifications depending on the specific location and type of the lesion. Under the older ICD-9-CM coding system, cholesteatoma was classified under code 385.3, with further specificity based on the anatomical site of the growth. What exactly is a cholesteatoma? A cholesteatoma is an abnormal, noncancerous skin growth that can develop in the middle section of your ear, behind the eardrum.
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The ICD-10 code for cholesteatoma of the middle ear is H71, which includes various sub-classifications depending on the specific location and type of the lesion. Under the older ICD-9-CM coding system, cholesteatoma was classified under code 385.3, with further specificity based on the anatomical site of the growth.
A cholesteatoma is an abnormal, noncancerous skin growth that can develop in the middle section of your ear, behind the eardrum. It often develops as a cyst or pouch that sheds layers of old skin. Over time, these skin cells accumulate, and the cholesteatoma can increase in size, potentially damaging the delicate bones of the middle ear or even affecting the inner ear, which can lead to hearing loss, dizziness, and ear drainage. While the term "tumor" is sometimes used, it is important to note that a cholesteatoma is not a form of cancer, though it requires medical intervention to prevent progressive damage to the auditory system.
Medical coding, such as the ICD-10 H71 series, is essential for physicians and hospitals to accurately document the diagnosis of cholesteatoma for insurance, research, and clinical tracking purposes. These codes allow healthcare systems to monitor the prevalence of the condition, which is significant given that over 1,133 members of the DiseaseMaps community have shared their personal experiences with this diagnosis. Precise coding helps in distinguishing between congenital cholesteatoma and acquired cholesteatoma, which is critical for determining the most appropriate surgical approach.
Identifying a cholesteatoma early is vital to preserving hearing and preventing complications. If you suspect you have this condition, look for these common clinical signs:
Because a cholesteatoma has the potential to erode bone and spread, surgery is the gold standard for treatment. The primary goal is to completely remove the diseased tissue and create a "safe" ear. Depending on the extent of the growth, this may involve a procedure known as tympanomastoidectomy. Following surgery, long-term monitoring is required, as there is a possibility of recurrence, necessitating regular follow-up appointments with an otolaryngologist.
Medical disclaimer: This content is for informational purposes only and does not constitute professional medical advice, diagnosis, or treatment; always seek the advice of your physician or other qualified health provider with any questions regarding a medical condition.