Occlusive disease of the carotid and basilar arteries has been studied extensively in adults, and with the advent of cerebral angiography, accurate anatomical diagnosis during life is now possible. Moreover, this method of investigation is being used with increasing frequency in pediatric problems, with the result that arterial occlusive disease is being encountered in a higher proportion of cases than might have been suspected. This report of two cases in children with major intracranial vascular occlusion was prompted by the infrequence of well-documented cases in the literature. The necropsy findings in the fatal case are presented, a review of selected cases from the literature is included in the discussion, and emphasis is placed upon the aid afforded by carotid angiography.
Report of CasesCase 1.\p=m-\An 11-year-old Negro girl with a left hemiparesis was admitted to the Bronx Municipal Hospital Center on Sept. 21, 1957. The child had been in good health and had a negative medical history except for an episode of minor head trauma one year previously. During the previous 2 weeks, she had intermittent mild right-sided headaches, but this did not interfere with her school work or usual play. On the day of admission, while at play, she suddenly developed a more severe right-sided headache and collapsed because of weakness of the left leg. The child was brought directly to the hospital.Examination.-Temperature 98 F, pulse 88, res¬ piration 16, blood pressure 120/60. The child was well developed and moderately obese. The general physical examination revealed no abnormalities. She was drowsy but well oriented and able to present the details of her illness. There was slight tenderness over the right temple. The pupils were normal, with the eyes in forced conjugate deviation to the right. There was a clear-cut dense left homonymous hemianopia. The optic fundi were normal. There was a marked left hemiparesis, including the face, with a left Babinski sign, depressed abdominal reflexes on the left, and hyporeflexia of the left arm and leg. A left-sided hemisensory defect was also present to all stimuli. The carotid pulsations in the neck were normal, and no bruit was audible in the neck or skull. Laboratory Data.-Blood cell count, including differential, and urinalysis were normal. Blood urea nitrogen was 12 mg. '% and a sickle-cell preparation was negative. Lumbar puncture re-