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CASE REPORT
Year : 2013  |  Volume : 19  |  Issue : 3  |  Page : 146-148

Congenital cholesteatoma with canal atresia: Three case reports


Department of ENT, Rajindra Hospital, Patiala, Punjab, India

Date of Web Publication2-Sep-2013

Correspondence Address:
Priyanka Aggarwal
9/865, Surgapuri, Muktsar Road, Kotkapura, Punjab - 151 204
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0971-7749.117465

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  Abstract 

In the present study, Congenital cholesteatoma is a rare entity in routine clinical practice. Secondary otitis media makes it difficult to diagnose. Chances of congenital cholesteatoma increase when it is associated with atretic ear. Appropriate imaging technique helps to diagnose and delineate the extent of congenital cholesteatoma. Computed tomography also plays a pivotal role in planning the surgery and grading the outcome of the surgery in congenital aural atresia. We had come across three such cases of congenital cholesteatoma with canal atresia along with conductive hearing loss and ear discharge. Meatoplasty with tympanomastoidectomy was carried out in these cases with hearing improvement confirmed by pure tone audiometry. Histopathology of soft-tissue material in all three cases showed cholesteatoma. Review of literature reveals that these conditions are rare.

Keywords: Canal atresia, Congenital cholesteatoma, Tympanomastoidectomy


How to cite this article:
Sohal BS, Aggarwal P, Goyal JP, Gupta A. Congenital cholesteatoma with canal atresia: Three case reports. Indian J Otol 2013;19:146-8

How to cite this URL:
Sohal BS, Aggarwal P, Goyal JP, Gupta A. Congenital cholesteatoma with canal atresia: Three case reports. Indian J Otol [serial online] 2013 [cited 2019 Jun 18];19:146-8. Available from: http://www.indianjotol.org/text.asp?2013/19/3/146/117465


  Introduction Top


Congenital malformation of external ear is often associated with malformation of middle and inner ear. Incidence of canal atresia is 1 in 10,000-20,000 live births with unilateral being more common than bilateral. External ear atresia is mostly bony rather than membranous; bony atresia of external ear is regularly associated with malformations of middle ear cavity and structures of middle-ear. [1]

Congenital cholesteatoma has been reported to be present in 4-7% of cases of congenital External auditory canal atresia.

Congenital cholesteatoma may originate from an epidermoid formation in the anterior superior lateral tympanic cavity adjacent to the anterior annulus during fetal development.

CT scan, especially, high-resolution CT scan is of great importance to delineate the extent of disease process and also to know the ossicular-chain status, condition of inner ear, and condition of seventh and eighth nerves. CT scan in case of congenital aural atresia also helps prognostically to predict the outcome of surgical correction.


  Case Reports Top


Case 1

A 30-year-old female patient presented with mastoid fistula with discharge on and off for the last 20-25 years along with history of deafness. She had atresia of left external ear canal since birth. There was no h/o trauma. On examination, pinna was normal in size and shape. Atresia of left ear canal was present (both bony and cartilaginous). A fistula was present near the tip of mastoid.

Tuning fork tests showed conductive hearing loss in left ear. Vestibular function tests were normal. Pure tone audiometry showed 50 dB conductive hearing loss with opposite ear normal hearing. CT scan showed absence of bony and cartilaginous external auditory canal and presence of cholesteatoma filling whole of middle ear cavity extending to mastoid. No ossicle was seen [Figure 1].
Figure 1: HRCT temporal bone case 1: Canal atresia with soft-tissue mass in middle-ear cavity

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Under General anaesthesia, mastoidectomy was carried out, cholesteatoma was removed and no ossicle was seen. The mastoid fistula was repaired and meatoplasty was carried out and the post-operative period was uneventful and the patient reported subjective improvement in hearing.

Case 2

A 24-year-old male presented with c/o discharge from the left ear since childhood and he had been scanty and continuous with no relief on repeated medication. The patient was a case of Down syndrome. There was a minute hole in the atretic left EAC from where foul smelling discharge was coming out. Chronic suppurative otitis media was present in the right ear too which was dry at the time of presentation. There was bony and cartilagenous canal atresia on left side. On CT, there was a cholesteatoma mass seen in the middle-ear cavity and no ossicle was present [Figure 2].
Figure 2: HRCT temporal bone for case 2: Bony and cartilagenous canal atresia with cholesteatoma mass

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Case was taken up under GA for mastoidectomy. Keeping in view that in such cases where no typical surgical landmarks are present and to avoid injury to the vital structures, the drilling was started from the small hole after giving post-auricular incision. The mastoid cavity was widened and the bony meatoplasty was carried out and the post-operative period was found to be uneventful.

Case 3

A 35-year-old male with microtia both ears presented with discharge from left side through a small hole in the skin in the region of EAC. On examination, no external auditory canal was visible. Discharge was foul smelling and there was s/o left facial nerve paresis.

Pure tone audiometry showed 55 dB of conductive hearing loss in the left ear. High resolution computed tomography left temporal bone showed bony and cartilagenous atresia of both ears. Cholesteatoma mass seen in the left ear cavity and there was no significant complaint in the right ear except mild hearing loss.

Case was taken up under GA. In this case, we faced some problem as pinna was not properly developed. The tragus was visualized and endaural type incision was given. A small hole in the bone [Figure 3] was identified from where the drilling was started and mastoidectomy with bony meatoplasty was carried out. No ossicle was seen and the post-operative period was uneventful with persistence of the left facial nerve paresis.
Figure 3: Intra-operative picture for case 3: Showing auricular skin tags and absent cartilagenous meatus

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The histopathological examination in all the three cases was suggestive of cholesteatoma.


  Discussion Top


Disorders of pinna and external auditory canal are common entity in clinical otology.

Both of the components of external ear-pinna and external auditory canal augment and transmit sound wave to tympanic membrane. Invagination of the ectodermal element of first pharyngeal pouch forms EAC. It grows medially to meet the endoderm of middle-ear. The mesodermal component gets entrapped between these ventral and dorsal sites giving rise to meatal plug or plate. This plate resorbs by the end of 28 th week of gestation and the external auditory canal recanalizes. Failure of recanalization leads to congenital aural atresia. [2]

Cholesteatoma is rarely a primary lesion (congenital cholesteatoma), originating from epithelial rests of ectodermal origin in the petrous bone, which may spread in and around the labyrinth and extend into the middle-ear cleft.

Congenital cholesteatoma may arise from cerebellopontine angle, petrous pyramid, jugular fossa, middle-ear cavity and mastoid antrum. [3] Acquired and congenital cholesteatoma are identical in their histopathological nature. They are keratin filled, epithelium-lined cysts that demonstrate linear growth pattern like skin. [4] Presence of otitis media is the only differentiating feature between acquired and congenital cholesteatoma.

Congenital cholesteatoma is usually silent but presents with complications such as otitis media, facial paralysis, hearing loss. Usually, the cause of infection is pseudomonas aeruginosa, bacillus proteus travelling along the  Eustachian tube More Details.

The diagnosis requires high-index of suspicion, knowledge of the sign and, symptoms produced by an expanding mass in the mastoid region and imaging study of this region. Clinical presentation depends on the site of lesion. If it is present in the middle ear cavity, it will manifest as deafness in early childhood; alternatively, if it is in petrous apex, patient will present with facial spasm in adulthood.

Imaging plays a major role in diagnosing and delineating the extent of the disease and planning for the surgery. [5] CT scan also plays pivotal role in planning the surgery and grading the outcome of the surgery in congenital aural atresia. A grading system based on pre-operative HRCT of the temporal bones was developed in an effort to select cases with chances of better outcome following atresia surgery. Pneumatisation of mastoid and presence of stapes have been the most important criteria for atresia surgery.

The cholesteatoma removal is preferred over prior reconstruction of hearing or canal reconstruction.

 
  References Top

1.Jahrsdoerfer RA. Congenital atresia of the ear. Laryngoscope 1978;88:1-48.  Back to cited text no. 1
    
2.Sadler TW. Langman's Medical Embryology. 7 th ed. Baltimore: Williams and Wilkins; 1995:77.  Back to cited text no. 2
    
3.Latack JT, Kartush JM, Kemink JL, Graham MD, Knake JE. Epidermoidomas of the cerebellopontine angle and temporal bone: CT and MR aspects. Radiology 1985;157:361-6.  Back to cited text no. 3
[PUBMED]    
4.Griffin C, DeLaPaz R, Enzmann D. MR and CT correlation of cholesterol cysts of the petrous bone. AJNR Am J Neuroradiol 1987;8:825-9.  Back to cited text no. 4
[PUBMED]    
5.Ghosh A, Saha S, Sadhu A, Saha PV. Imaging of congenital cholesteatoma with atretic ear: A rare case report. Indian J Radiol Imaging 2006;16:673-5.  Back to cited text no. 5
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    Figures

  [Figure 1], [Figure 2], [Figure 3]



 

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