Biomedical subjects
Publications and source records attributed to R J Stark.
A young epileptic presented with spasticity as well as ataxia, diplopia and nystagmus; his serum phenytoin level was very high. All the abnormal signs disappeared after withdrawal of phenytoin. Spasticity, hyperreflexia, and clonus are features of phenytoin intoxication, present in this case, which are not commonly seen, and which have rarely been mentioned previously in the literature.
A case of eosinophilic polymyositis is reported. Tender muscle swelling was followed by proximal weakness, creatinine kinase elevation, and electromyographic features typical of polymyositis. Severe myocarditis, pericarditis and heart failure were present. Muscle biopsy specimen showed active myositis with eosinophil infiltrate. Unlike previous cases, blood eosinophils count was normal. The clinical response to corticosteroids was excellent, and a relapse occurring as steroid dose was lowered responded rapidly to an increased dose of prednisolone. Eosinophilic polymyositis may be a component of a general systemic illness with prominent cardiac involvement.
In two patients, large aneurysms of the basilar artery produced a supranuclear gaze paresis, involving horizontal gaze in one case and vertical gaze in the other. In both cases the diagnosis was suggested by computed tomography and confirmed by vertebral angiography. Autopsy findings in one case confirmed the diagnosis. Although supranuclear gaze palsies must reflect damage to structures deep within the brain stem, these cases illustrate that an extrinsic lesion may produce such damage indirectly. Basilar artery aneurysm should be considered in patients presenting with supranuclear gaze paresis and long tract signs.
A woman presented with severe weakness and wasting involving only one arm. A definite diagnosis was not made until almost six years later when she developed proximal weakness in the legs as well, and a muscle biopsy showed changes of polymyositis. Asymmetry of weakness in polymyositis has been noted previously in the literature, but is rare. In previous reports asymmetry as marked as in the present case has not been noted.