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Original Article |

Patulous Internal Auditory Canal FREE

Lela Migirov, MD
[+] Author Affiliations

From the Department of Otolaryngology–Head and Neck Surgery, Sheba Medical Center, Tel Hashomer, Israel, and Tel Aviv University, Tel Aviv, Israel. The author has no relevant financial interest in this article.


Arch Otolaryngol Head Neck Surg. 2003;129(9):992-993. doi:10.1001/archotol.129.9.992.
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Objective  To investigate a rare anomaly of the internal auditory canal known as a patulous canal and its relationship to hearing impairment.

Methods  High-resolution computed tomographic scans of the temporal bones of patients who presented between August 2001 and August 2002 were reviewed. The patients' medical charts were evaluated for age, sex, and hearing impairment, and the computed tomographic scans were examined for the presence of a patulous canal.

Results  The study group included 645 patients who underwent high-resolution computed tomography of the temporal bones for various reasons, including sensorineural hearing loss (50% of patients). A patulous canal without any associated anomaly of the labyrinth was the only finding in 2 patients. Both patients had chronic middle ear disease along with conductive hearing loss.

Conclusion  Patulous canal is a rare anatomical variant of the internal auditory canal (0.3%), and its association with inflammatory ear disease accompanied by conductive hearing impairment appears to have been incidental in both cases in the present study.

Figures in this Article

DILATED INTERNAL auditory canals (IACs) have been found in association with impaired hearing in patients without evidence of acoustic neuromas.13 In the present study, an anatomical variant of the IAC known as patulous canal and its relationship to hearing loss were investigated. This anomaly is almost invariably bilateral and is characterized by increased height at the midportion of the IAC.4

High-resolution computed tomographic (CT) scans of the temporal bones of patients who presented between August 2001 and August 2002 were reviewed. The patients' medical charts were evaluated for age, sex, and hearing impairment, and the CT scans were examined for the presence of a patulous canal.

The study group consisted of 645 patients who had undergone CT scans of the temporal bones for various reasons, including sensorineural hearing loss (50% of patients). The age of the patients ranged from 1 month to 73 years. A patulous canal without any associated anomaly of the labyrinth was the only finding in 2 men (Figure 1). One of them had a prolonged history of bilateral chronic secretory otitis media and mild conductive hearing loss. The other one underwent tympanoplasty and correction of the lateralized eardrum in both ears. The chronic ear disease in the latter patient was accompanied by mild conductive hearing impairment.

Place holder to copy figure label and caption

High-resolution computed tomographic scan of the temporal bones shows a patulous canal (arrowheads) in both ears.

Graphic Jump Location

High-resolution CT of the temporal bone is an important modality for the evaluation of bony abnormalities of the ear. In 1964, Valvassori5 concluded that a normal IAC ranges from 2.0 to 9.0 mm in diameter, with less than 2 mm of difference between 2 sides. To my knowledge, there is not a lot of information about the patulous canal. This anomaly is characterized by a bilateral, usually symmetrical, increase in height at the midportion of the IAC.4 The patulous canal differs from dilatation that results from acoustic neuromas because of the presence of cortical margins of the canal and the absence of any destruction of the crista falciformis. The significance of a dilated IAC in the pathogenesis of hearing impairment is questionable.

Swartz and Harnsberger6 found a strikingly wide IAC in both ears of an elderly patient with profound sensorineural hearing loss that had begun very early in life. The nerves appeared somewhat small on an air cisternographic study. The reason for this striking development variation was not known. Davis and Rumbaugh2 reported that patulous canals may appear in patients with a sensorineural hearing loss of undefined etiology.

Jensen1 reported that among 62 deaf children, the CT scans of 2 brothers, 1 with retinitis pigmentosa, revealed extreme dilatation in the lateral portion of the IAC. Jensen also described 3 boys who had an enlarged vestibule, an irregularly dilated cochlear lumen, a dilated lateral end of the IAC, and an associated mixed hearing loss of about 60 dB. Phelps7 found that a dilated and dysplastic labyrinth, with a wide medial end of the internal acoustic meatus, may be associated with spontaneous cerebrospinal fluid fistulae and an absence of cochlear function in the affected ears. Weinberg et al4 described 3 patients with enlarged IACs and normal hearing. They suggest that the height increase of the posterior medial aspect of the canal is due to a congenital developmental variant of the temporal bone.

In the present study, a patulous canal was found in 2 (0.3%) of 645 patients who underwent high-resolution CT scans of the temporal bones for various reasons, and the shape of the canal was not associated with any anomaly of the labyrinth. A patulous canal accompanied by sensorineural hearing loss was not found. The patulous canal is a rare anatomical variant of the IAC, and I suggest that in the 2 cases described herein its association with inflammatory ear disease and related conductive hearing impairment was incidental.

Corresponding author: Lela Migirov, MD, Department of Otolaryngology–Head and Neck Surgery, Sheba Medical Center, Tel Hashomer 5262l, Israel (e-mail: kro@zahav.net.il).

Submitted for publication September 25, 2002; final revision received November 5, 2002; accepted November 11, 2002.

Jensen  J Congenital anomalies of the inner ear. Radiol Clin North Am.1974;12:473-482.
PubMed
Davis  DORumbaugh  CL Temporal bone.  In: Newton  TH, Potts  DG, eds. Radiology of the Skull and Brain. St Louis, Mo: Mosby–Year Book Inc; 1971:431-520.
Lin  SRLee  KFStein  GNLee  I Asymmetrical internal auditory canals. Arch Otolaryngol.1973;98:164-169.
PubMed
Weinberg  PEKim  KSGore  RM Unilateral enlargement of the internal auditory canal: a developmental variant. Surg Neurol.1981;15:39-42.
PubMed
Valvassori  GE The radiological diagnosis of acoustic neuromas. Arch Otolaryngol.1966;83:582-587.
PubMed
Swartz  JDHarnsberger  HR The otic capsule and otodystrophies.  In: Imaging of the Temporal Bone.3rd ed. New York, NY: Thieme Medical Publishers; 1998:240-317.
Phelps  PD Congenital cerebrospinal fluid fistulae of the petrous temporal bone. Clin Otolaryngol.1986;11:79-92.
PubMed

Figures

Place holder to copy figure label and caption

High-resolution computed tomographic scan of the temporal bones shows a patulous canal (arrowheads) in both ears.

Graphic Jump Location

Tables

References

Jensen  J Congenital anomalies of the inner ear. Radiol Clin North Am.1974;12:473-482.
PubMed
Davis  DORumbaugh  CL Temporal bone.  In: Newton  TH, Potts  DG, eds. Radiology of the Skull and Brain. St Louis, Mo: Mosby–Year Book Inc; 1971:431-520.
Lin  SRLee  KFStein  GNLee  I Asymmetrical internal auditory canals. Arch Otolaryngol.1973;98:164-169.
PubMed
Weinberg  PEKim  KSGore  RM Unilateral enlargement of the internal auditory canal: a developmental variant. Surg Neurol.1981;15:39-42.
PubMed
Valvassori  GE The radiological diagnosis of acoustic neuromas. Arch Otolaryngol.1966;83:582-587.
PubMed
Swartz  JDHarnsberger  HR The otic capsule and otodystrophies.  In: Imaging of the Temporal Bone.3rd ed. New York, NY: Thieme Medical Publishers; 1998:240-317.
Phelps  PD Congenital cerebrospinal fluid fistulae of the petrous temporal bone. Clin Otolaryngol.1986;11:79-92.
PubMed

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