Legal disclaimers in medical journals and textbooks.
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Biomedical subjects
Publications and source records attributed to W M Hendricks.
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Twenty-one patients with stasis leg ulcers were randomly assigned to two groups. The first group was treated with Unna's boots, while the second was treated with elastic support stockings with graded compression from 24 mm/Hg pressure at the ankle to 16 mm/Hg pressure at the calf. The ulcers on seven of ten legs (70%) treated with Unna's boots and on 10 of 14 legs (71%) treated with elastic support stocking healed. Although the two groups were small, there was no statistically significant difference between their success rate in healing stasis leg ulcers (p = 0.9394). Both treatment groups showed significant changes in lower limb volume, calf circumference, and ankle circumference, although there was no statistically significant difference between the two groups. If healing times are calculated, however, the average healing time in the Unna boot-treated group was 7.3 weeks, while patients treated with support stockings took an average of 18.4 weeks. If one patient whose ulcerations almost encircled her calves and took 78 weeks to heal is excluded, patients treated with support stockings had an average healing time of 11.8 weeks.
A newborn baby with generalized "blueberry muffin" eruption and histologic evidence of dermal erythropoiesis is described. This case is unusual in that we could not identify any of the congenital viral infections usually associated with this syndrome. The clinical features of dermal erythropoiesis and dermal hematopoiesis are reviewed briefly.
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A 14-year-old boy developed a cluster of blue nevi after a severe sunburn. The relationship between cutaneous injury and the development of blue nevi is discussed.
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Oculoauriculovertebral dysplasia is a developmental disorder characterized by a triad of anomalies; epibulbar dermoids with or without lipodermoids, preauricular appendages or blind preauricular fistulae, and vertebral anomalies. Multiple associated anomalies have been reported. A case of this syndrome and a review of the literature are presented herein.
A review of Weber-Christian syndrome in infancy is presented along with the report of two cases. Both infants had low serum properdin levels, and one patient showed remissions of his disease when he was T-lymphocytopenic. This suggests that the T-lymphocyte may have an important role in the pathogenesis of Weber--Christian syndrome.