Congenital Cholesteatoma with Mastoid and Temporal Epidural Abscess in a Patient with Congenital Aural Atresia and Grade II Microtia: A Case Report
DOI:
https://doi.org/10.38035/ijphs.v4i3.2302Keywords:
Congenital Cholesteatoma, Congenital Aural Atresia, Microtia, Mastoid Abscess, Epidural AbscessAbstract
Congenital cholesteatoma arising in an ear with congenital aural atresia is a rare entity, and diagnosis is difficult because the atretic plate prevents otoscopic assessment of the tympanic membrane. A 17-year-old male with left grade II microtia and congenital aural atresia presented with worsening left-sided headache, fever, severe mixed hearing loss, and recurrent purulent discharge from a left retroauricular fistula. Temporal computed tomography and contrast-enhanced magnetic resonance imaging showed chronic otomastoiditis with an extensive cholesteatoma eroding the temporal bone, destroying the tegmen tympani, and forming a mastoid abscess extending into the left temporal epidural space. A combined procedure was performed, comprising craniotomy with abscess evacuation and pericranial dural grafting by neurosurgery together with subtotal petrosectomy and abdominal fat obliteration by otolaryngology. Intraoperatively the ossicular chain was fused and no continuity was found between the cholesteatoma matrix and external canal skin, supporting a congenital origin. Culture grew Proteus mirabilis. Symptoms resolved initially, but retroauricular discharge recurred five months postoperatively, after which the patient was lost to follow-up. Congenital aural atresia conceals cholesteatoma from clinical examination, so cross-sectional imaging carries the diagnosis. Disease of this extent warrants structured long-term surveillance.
References
Abdel-Aziz, M. (2012). Congenital cholesteatoma of the infratemporal fossa with congenital aural atresia and mastoiditis: a case report. BMC Ear, Nose and Throat Disorders, 12(1), 6. https://doi.org/10.1186/1472-6815-12-6
Abell, B. D., Bothwell, S., Hedman, M. E., Adkisson, K. H., Darr, O. A., Herrmann, B. W., & Gitomer, S. A. (2025). Audiometric trends among children with congenital aural atresia or external auditory canal stenosis. Laryngoscope, 135(11), 4433–4441. https://doi.org/10.1002/lary.32321
Aggarwal, P., & Rayamajhi, P. (2020). Congenital cholesteatoma in a case of congenital aural atresia: A case report. JNMA J Nepal Med Assoc, 58(232), 1080–1082. https://doi.org/10.31729/jnma.5199
Amoodi, H., Mofti, A., Fatani, N. H., Alhatem, H., Zabidi, A., & Ibrahim, M. (2022). Non-echo planar diffusion-weighted imaging in the detection of recurrent or residual cholesteatoma: A systematic review and meta-analysis of diagnostic studies. Cureus, 14(12), e32127. https://doi.org/10.7759/cureus.32127
Bonnard, Å., Engmér Berglin, C., Wincent, J., Eriksson, P. O., Westman, E., Feychting, M., & Mogensen, H. (2023). The Risk of Cholesteatoma in Individuals with First-degree Relatives Surgically Treated for the Disease. JAMA Otolaryngology–Head & Neck Surgery, 149(5), 390. https://doi.org/10.1001/jamaoto.2023.0048
Chan, C. Y., Karmali, S. A., Arulanandam, B., Nguyen, L. H. P., & Duval, M. (2023). Cholesteatoma in congenital aural atresia and external auditory canal stenosis: A systematic review. Otolaryngol Head Neck Surg, 169(3), 449–453. https://doi.org/10.1177/01945998221094230
Gagnier, J. J., Kienle, G., Altman, D. G., Moher, D., Sox, H., & Riley, D. (2014). The CARE guidelines: Consensus-based clinical case report guideline development. J Clin Epidemiol, 67(1), 46–51. https://doi.org/10.1016/j.jclinepi.2013.08.003
Govindan, A., Fiest, C., Chou, D. W., Saade, M., Gray, M., & Cosetti, M. (2025). Genetics of nonsyndromic microtia and congenital aural atresia: A scoping review. Otolaryngol Head Neck Surg, 172(3), 811–820. https://doi.org/10.1002/ohn.1060
Grinblat, G., Vlad, D., Caruso, A., & Sanna, M. (2020). Evaluation of subtotal petrosectomy technique in difficult cases of cochlear implantation. Audiol Neurootol, 25(6), 323–335. https://doi.org/10.1159/000507419
Handoko, E., Handoko, R. E., & Wahyudi, A. D. (2026). Evaluating long-term recurrence of cholesteatoma following primary surgery: An umbrella review of surgical techniques and patient factors. J Laryngol Otol, 1–7. https://doi.org/10.1017/S0022215126105234
Haritha, S., Reddy Yalaka, M., Pratyusha Polepeddi, S., Birudaraju, S. S., Babu, S., & Padmanabhan, S. (2025). Congenital external auditory canal atresia with coexistent congenital cholesteatoma. Ear Nose Throat J, 104(9), 550–552. https://doi.org/10.1177/01455613221142121
Jamarun, S. A. B., Ong, C. A., Anastasius, E. J., & Goh, B.-S. (2025). Danger of delay: A case report of a hidden, extensive, congenital external auditory canal cholesteatoma in a pediatric patient. Cureus, 17(4), e81938. https://doi.org/10.7759/cureus.81938
Kelley, P. E., & Scholes, M. A. (2007). Microtia and Congenital Aural Atresia. Otolaryngologic Clinics of North America, 40(1), 61–80. https://doi.org/10.1016/j.otc.2006.10.003
Levenson, M. J., Parisier, S. C., Chute, P., Wenig, S., & Juarbe, C. (1986). A review of twenty congenital cholesteatomas of the middle ear in children. Otolaryngol Head Neck Surg, 94(5), 560–567. https://doi.org/10.1177/019459988609400505
Mazita, A., Zabri, M., Aneeza, W. H., Asma, A., & Saim, L. (2011). Cholesteatoma in patients with congenital external auditory canal anomalies: retrospective review. The Journal of Laryngology & Otology, 125(11), 1116–1120. https://doi.org/10.1017/S0022215111002052
Mohamed Ali, I., Duman, C., Bozdag, I., Artan Abdi, A., Nor Abdi, M., Karakurt, S. E., & Yigit, O. (2022). Microbiology and drug susceptibility pattern of bacterial isolates from patients with chronic suppurative otitis media at a tertiary care hospital in Somalia. Infect Drug Resist, 15, 7733–7739. https://doi.org/10.2147/IDR.S390886
Park, E., Lee, G., Jung, H. H., & Im, G. J. (2019). Analysis of inner ear anomalies in unilateral congenital aural atresia combined with microtia. Clin Exp Otorhinolaryngol, 12(2), 176–180. https://doi.org/10.21053/ceo.2018.00857
Popescu, C., Varut, R. M., Puticiu, M., Belghiru, V. I., Banicioiu, M., Rotaru, L. T., Popescu, M., Cosmin, A. C., & Popescu, A. I. S. (2024). Comprehensive management of cholesteatoma in otitis media: Diagnostic challenges, imaging advances, and surgical outcome. J Clin Med, 13(22), 6791. https://doi.org/10.3390/jcm13226791
Sitompul, B. P., & Handoko, E. (2023). Kolesteatoma Kongenital pada Atresia Canalis Acousticus Externus Kongenital Unilateral dan Mikrotia Grade I. Malang Otorhinolaryngology Head and Neck Surgery Journal, 2.
Sohal, B., Aggarwal, P., Goyal, J., & Gupta, A. (2013). Congenital cholesteatoma with canal atresia: Three case reports. Indian Journal of Otology, 19(3), 146. https://doi.org/10.4103/0971-7749.117465
Tabook, S. M. S., Abdel Tawab, H. M., & Gopal, N. K. (2015). Congenital Cholesteatoma Localized to the Mastoid Cavity and Presenting as a Mastoid Abscess. Case Reports in Otolaryngology, 2015, 1–3. https://doi.org/10.1155/2015/305494
Volgger, V., Lindeskog, G., Krause, E., & Schrötzlmair, F. (2020). Identification of risk factors for residual cholesteatoma in children and adults: a retrospective study on 110 cases of revision surgery. Brazilian Journal of Otorhinolaryngology, 86(2), 201–208. https://doi.org/10.1016/j.bjorl.2018.11.004
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