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chronic suppurative otitis media

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2 OTOLARYNGOLOGY<br />

progressive brain stem displacement and cerebellar involvement. Diplopia due to pressure on the VIth<br />

cranial nerve, and hoarseness with dysphagia due to involvement of the IXth and Xth nerves is rare.<br />

5. Terminal symptoms. The raised CSF pressure causes failing vision due to papilloedema, headache,<br />

alteration in conscious level and eventually coma.<br />

In the otological phase, general examination will usually reveal no abnormalities. The patient may have a<br />

unilateral neural hearing loss. Hypaesthesia of the posterior external ear canal on the side of the hearing loss<br />

should raise the index of suspicion (Hitselberger sign). Loss of the corneal reflex is an early sign of<br />

trigeminal nerve impairment. Nystagmus when present may be of the vestibular or cerebellar type. Facial<br />

nerve impairment is usually of the sensory element and can be elicited as a lack of taste on<br />

electrogustometry or loss of lacrimation on Schirmer’s test. Slight facial weakness may show as a delay in<br />

the blink reflex. Later the patient may have evidence of ataxia. Neurological signs of the other cranial nerve<br />

palsies will eventually become apparent.<br />

Investigations<br />

1. Radiological investigations. The most accurate means of identifying small intracanalicular tumours is<br />

magnetic resonance imaging (MRI) with gadolinium enhancement. This is therefore the investigation of<br />

choice and is used for screening. Computerized tomography (CT) scanning with high definition and<br />

enhancement techniques will accurately diagnose and delineate most tumours, but should only be used<br />

when MRI is unavailable.<br />

2. Audiometry. A unilateral or asymmetrical sensorineural hearing loss can usually be demonstrated by a<br />

pure tone audiogram. The hearing loss is classically a neural lesion with no loudness recruitment,<br />

abnormally rapid adaptation and disproportionately poor speech discrimination. Stapedial reflex decay can<br />

be measured using impedance audiometry, and this gives a low-false negative rate of around 5%. Brainstem<br />

electric response audiometry has only a 3% false-negative rate. It demonstrates a retrocochlear lesion by an<br />

increased latency between N1 and N5 waves. If the pure tone threshold hearing loss is greater than 70 dB,<br />

the accuracy of audiometric testing is poor.<br />

3. Vestibular investigations. Caloric responses are usually reduced in or absent from the affected side, but<br />

there is no abnormality in some patients with small tumours. Special audiometric and vestibular testing are<br />

now rarely, if ever, used for the diagnosis of an acoustic neuroma.<br />

Differential diagnosis of a tumour at the cerebellopontine angle<br />

1. Acoustic neuromas (constitute 80% of cerebellopontine angle tumours).<br />

2. Meningioma.<br />

3. Neuroma of the VIIth nerve.<br />

4. Congenital cholesteatoma.<br />

5. Aneurysm of the basilar or vertebral arteries.<br />

6. Cholesterol granuloma of the petrous apex.<br />

7. Cerebellar tumour.<br />

Management<br />

The ideal management is a single stage total removal of the lesion, with preservation of all neural function<br />

and with minimal morbidity and mortality. However, this ideal is not always possible. Each case must be

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