Imaging of congenital middle ear deafness.

نویسندگان

  • T Y Tan
  • J P Goh
چکیده

INTRODUCTION Conductive hearing loss, in the presence of a normal external ear, is usually due to an interference with the normal transmission of sound from the tympanic membrane across the ossicular chain to the oval window. If conductive hearing loss occurs in a young child, congenital middle ear pathology is the most likely cause. MATERIALS AND METHODS High resolution computed tomography of the middle ear is the diagnostic modality of choice. Details of the imaging technique are outlined in this article. Eight cases of congenital middle ear deafness imaged in the radiological departments of Changi General Hospital and Tan Tock Seng Hospital in Singapore are illustrated. RESULTS Congenital middle ear deafness may be classified into ossicular chain abnormalities, congenital ossicular fixation, congenital oval window atresia and congenital round window atresia. The imaging features for each category are described. CONCLUSION With proper imaging technique and a systemic analysis of the images, the abnormalities that result in congenital middle ear deafness can usually be demonstrated on most occasions.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

CLASSIFICATION OF CONGENITAL MIDDLE AND EXTERNAL EAR MALFORMATIONS: CT STUDY

The authors used high-resolution computed tomography (HRCT) for studying 52 congenitally malformed ears in 45 children between five and 10 years of age. In six children the malformations were bilateral. The malformations clinically manifested as microtia, atresia of the external auditory canal and conductive deafness. Analyzing anatomical details and pathological changes on HRCT axial sec...

متن کامل

Original Solution for Middle Ear Implant and Anesthetic/Surgical Management in a Child with Severe Craniofacial Dysmorphism

We describe the novel solution adopted in positioning middle ear implant in a child with bilateral congenital aural atresia and craniofacial dysmorphism that have posed a significant challenge for the safe and correct management of deafness. A five-year-old child, affected by a rare congenital disease (Van Maldergem Syndrome), suffered from conductive hearing loss. Conventional skin-drive bone-...

متن کامل

Congenital bifurcation of the intratemporal facial nerve.

Anomalies of the course of the facial nerve have been reported in association with middle and inner ear malformations. Bifurcation of its intratemporal portion is a rare malformation in which focal splitting of one or more facial nerve segments occurs. We describe the CT appearance of this anomaly and discuss its possible embryology. Facial nerve bifurcation is important to recognize in patient...

متن کامل

The Rottenrow endotracheal tube holder.

Case 3 is a rare congenital abnormality of the inner ear which usually presents as recurrent meningitis. This abnormality is now well documented.4 It should be suspected as a cause of recurrent meningitis in a child who has a sensorineural deafness. The presence of fluid behind the tympanic membrane should make one suspicious and the diagnosis can be confirmed by tomograms of the inner ear. The...

متن کامل

Surgical method for virally mediated gene delivery to the mouse inner ear through the round window membrane.

Gene therapy, used to achieve functional recovery from sensorineural deafness, promises to grant better understanding of the underlying molecular and genetic mechanisms that contribute to hearing loss. Introduction of vectors into the inner ear must be done in a way that widely distributes the agent throughout the cochlea while minimizing injury to the existing structures. This manuscript descr...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Annals of the Academy of Medicine, Singapore

دوره 32 4  شماره 

صفحات  -

تاریخ انتشار 2003