Biomedical subjects
S B Mallory
Publications and source records attributed to S B Mallory.
Osteoma cutis as a presenting sign of pseudohypoparathyroidism.
Four unrelated children with osteoma cutis and Albright hereditary osteodystrophy (pseudohypoparathyroidism and pseudopseudohypoparathyroidism) are described. All four patients were normocalcemic when they were first seen with cutaneous ossification. A diagnosis of Albright hereditary osteodystrophy was established on the basis of associated somatic features, radiographic abnormalities, and family history. Progression to pseudohypoparathyroidism was documented in two children who developed hypocalcemia at 2 and 3 years of age, respectively. Early recognition of the skin manifestations of this syndrome and careful follow-up are important to prevent the deleterious effects of hypocalcemia. Osteoma cutis is a common sign of Albright hereditary osteodystrophy in infancy and childhood, and its significance should not be overlooked, even in the normocalcemic patient.
What syndrome is this? Klippel-Trenaunay syndrome.
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Name this syndrome. Incontinentia pigmenti.
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Segmental eruption in an 8-year-old girl.
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Azithromycin compared with cephalexin in the treatment of skin and skin structure infections.
This randomized, third-party-blinded study compared short-course therapy of once-daily azithromycin (500 mg on day 1, followed by 250 mg/day on days 2-5) with cephalexin (500 mg twice daily for 10 days) in the treatment of patients with skin and skin structure infections. At 25 centers, a total of 361 patients were entered into the study and 148 were evaluable for efficacy. The main causative pathogens, Staphylococcus aureus and Streptococcus pyogenes, were responsible for approximately two thirds of the infections in the two treatment groups. Clinical cure and improvement rates for the two treatments were comparable; 99% with azithromycin and 96% with cephalexin. On completion of therapy, both treatments had eradicated approximately 98% of pathogens. In general, both agents were well-tolerated. The results of this study show that a 5-day course of once-daily treatment with azithromycin is as effective as a 10-day course of twice-daily treatment with cephalexin in the management of skin and skin structure infections.
Diffuse papular eruption with swelling of joints in a preschooler. Sarcoidosis in a preschooler.
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Blau syndrome versus sarcoidosis.
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Neonatal skin disorders.
Skin disorders are commonly seen in the neonatal period. A recent survey of neonates demonstrated that almost every neonate had some skin lesion. The most common skin findings are desquamation, Epstein's pearls, sebaceous hyperplasia, milia, toxic erythema, salmon patch, hypertrichosis, and Mongolian spot. In addition to these common cutaneous findings, other disorders may exist and are discussed in this article.
Congenital immunodeficiency syndromes with cutaneous manifestations. II.
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Acquired forms of immunosuppression.
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Reticulate acropigmentation of Kitamura with localized alopecia.
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Infantile myofibromatosis.
Infantile myofibromatosis is part of a heterogeneous group of rare childhood fibromatoses characterized by the proliferation of myofibroblasts. It is not a common condition and is frequently misdiagnosed. We present an unusual patient who had small, depressed, atrophic, skin lesions uncharacteristic of infantile myofibromatosis.
What syndrome is this characteristic of? Dyskeratosis congenita.
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Warts in blacks versus whites.
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Atopic dermatitis and food hypersensitivity in children.
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Congenital immunodeficiency syndromes with cutaneous manifestations. I.
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Ulerythema ophryogenes in Noonan syndrome.
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