Hearing loss is not a diagnosis; rather it is a symptom, and patients require careful assessment. The Royal National Institute for the Deaf proposes that hearing aid dispensers should perform this function. Failure ?r.Atedj 1989;299:439-41 Since the introduction of computed tomography (CT) small or asymptomatic chronic subdural haematomas have been recognised with increasing frequency, though their detection may depend on the use of contrast enhancing agents.' Patients with chronic subdural haematoma commonly present with headache, disturbances of higher cerebral function such as personality change and confusion, or features of raised intracranial pressure. Hemiparesis, with dysphasia if the lesion is over the dominant hemisphere, is the most frequent focal neurological deficit. Epilepsy is traditionally thought of as a rare presenting feature.) We describe a patient in whom several different forms of epilepsy were the only clinical manifestations of a very small chronic subdural haematoma.
Case historyA 75 year old man was admitted after a witnessed tonic-clonic convulsion. Over the previous two weeks he had suffered three episodes of sudden, complete inability to speak, during which he remained fully conscious without any abnormal movements being noted. Each episode lasted about five minutes. He was seen by his general practitioner, who diagnosed transient ischaemic attacks but did not prescribe aspirin. The patient denied headache, and neither he nor his family could recall any recent head injury. He was taking chlorpropamide for maturity onset diabetes but there was no previous history of epilepsy or cerebrovascular disease. He had never had an excessive alcohol intake. Full neurological examination on admission showed nothing abnormal, and in particular there was no disturbance of higher cerebral function. Blood glucose, electrolyte, and calcium concentrations remained normal throughout.Over the next 24 hours attacks were witnessed during which the patient would become vacant and his head and eyes would deviate to the right. His right arm would then become elevated with external rotation of the shoulder followed by alternating flexion and extension at the elbow while the wrist remained flexed and the fingers extended and abducted. These attacks would last between five and 60 seconds and were followed by a variable period of confusion. They could occur several times an hour, often without complete recovery of consciousness in between. During periods of full consciousness, however, no neurological deficit could be detected. An attack could be terminated with intravenous diazepam, which would continue to act for about 30 minutes. He was given a loading dose of intravenous phenytoin followed by conventional oral doses.About 48 hours after admission a further change was noted, in that he was continuously confused with a fluctuating level of consciousness. On occasions he BMJ VOLUME 299 12 AUGUST 1989 439