Objective-To describe the incidence of pediatric Horner syndrome and the risk of occult malignancy in a population-based cohort.Methods-The medical records of all pediatric patients (aged <19 years) residing in Olmsted County, Minnesota, who received diagnoses of Horner syndrome from January 1, 1969, through December 31, 2008, were retrospectively reviewed.
Results-HornerSyndrome was diagnosed in 20 pediatric patients during the 40-year period, yielding an age-and sex-adjusted incidence of 1.42 per 100 000 patients younger than 19 years of age (95% confidence interval [CI]: 0.80-2.04). Eleven of the 20 patients (55%) had a congenital onset, for a birth prevalence of 1 in 6250 (95% CI: 3333-10 000), while the remaining 9 (45%) had acquired syndromes. Seven of the 11 (63.6%) patients with congenital cases had a history of birth trauma, while the remaining 4 (36.4%) had no identifiable cause. Six of the 9 (66%) acquired cases occurred following surgery or trauma while the remaining 3 (33%) had no known etiology. None (95% CI: 0.0-16.8%) of the 20 patients were found to have a neuroblastoma or other malignancy during a mean following of 56.5 months (range, 0-256.9 months).