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Biomedical subjects

R C Hansen

Publications and source records attributed to R C Hansen.

At least 55 records · Page 3Linked to original sources

Urticarial vasculitis treated with colchicine.

Cutaneous vasculitis may present as an urticaria-like eruption in association with viral illness, systemic lupus erythematosus, Sjögren's syndrome, or serum sickness. Often, however, urticarial vasculitis presents as an immune complex-mediated disease without other associated connective-tissue disease or associated infection. Many forms of therapy have been tried, including antihistamines, prednisone, and immunosuppressive drugs without success in every patient. Because colchicine had been effective in some patients with non-urticarial cutaneous vasculitis, we decided to use it in two patients with urticarial vasculitis in whom other therapy had failed. Both responded dramatically, although severe hypocomplementemia persisted in one patient.

Adult↗

Necrotizing fasciitis in infancy: report of three cases and review of the literature.

Necrotizing fasciitis exists on a continuum of soft tissue infections between cellulitis and myonecrosis. It has been uncommonly reported in infancy (1-10). The diagnosis depends on recognition of the characteristic rapidly progressive clinical course and demonstration of full-thickness skin necrosis with involvement of the fascial planes overlying the muscle. The organisms most often recovered are beta-hemolytic Streptococcus or Staphylococcus aureus, but other aerobic and anaerobic organisms in single or mixed infection have been reported (1, 2, 11, 12). This infection has a significant mortality rate, necessitating early, aggressive, specific medical and surgical treatment.

Fasciitis↗

Staphylococcal scalded skin syndrome, toxic shock syndrome, and Kawasaki disease.

Three dramatic clinical syndromes have been compared and contrasted. Of these, staphylococcal scalded syndrome is most readily recognized and least likely to have a morbid or fatal outcome. It is easy to confuse toxic shock syndrome and Kawasaki disease. Since the case fatality rate is significant in both of these diseases, and the management so different, proper recognition of the disease by its external features is critical.

Adolescent↗

Cystic fibrosis manifesting with acrodermatitis enteropathica-like eruption. Association with essential fatty acid and zinc deficiencies.

A refractory dermatitis resembling acrodermatitis enteropathica was the manifesting sign in a 5-month-old male infant with cystic fibrosis, preceding pulmonary and gastrointestinal tract symptoms by two months. The eruption was clearly nutritionally responsive. Biochemical evidence was shown for deficiencies of zinc, essential fatty acids, and protein. Altered prostaglandin metabolism was also demonstrated.

Acrodermatitis↗

Atypical familial benign chronic pemphigus.

Two patients with atypical features of familial benign chronic pemphigus (FBCP) are presented herein. One patient had lesions limited to the anterior chest and the other had lesions localized to the lateral arms. Neither patient had prominent intertriginous involvement. These cases illustrate the protean manifestations of this disease.

Adult↗

Punctate hyperkeratosis of the palms and soles. An ultrastructural study.

Punctate hyperkeratosis of the palms and soles is an uncommon autosomal dominant condition. We report a 65-year-old man with this condition and review the literature. With electron microscopy, we have examined both clinically affected and adjacent clinically unaffected palmar skin. The only ultrastructural differences noted were a thicker keratin layer and hypertrophic nucleoli in the basal cell layer and stratum spinosum in the clinically affected skin. This nucleolar hypertrophy suggests that there may be increased metabolic activity in the clinically affected skin which is contributing to the abnormal keratinization.

Aged↗

The blue-gray cystic basal cell epithelioma.

We report, in two men, the occurrence of a tiny, dome-shaped, blue-gray cystic nodule of the face. The nodule in both men clinically simulated an eccrine or apocrine hidrocystoma. Histologic examination revealed that both were cystic basal cell epitheliomas. These cases are reported in order to bring this unusual clinical presentation of basal cell epithelioma to the attention of clinicians.

Basal Cell Carcinoma↗

Transcutaneous gamma benzene hexachloride absorption and toxicity in infants and children.

A premature, malnourished infant had seizures and abnormal neurological function associated with topical gamma benzene hexachloride (lindane) therapy. The level of gamma benzene hexachloride in his blood was 17 times greater than expected after a single topical application of 1% gamma benzene hexachloride. Significant levels developed in another child's blood after repeated applications of small amounts to areas of dermatitis and excoriations on the skin. The use of topical gamma benzene hexachloride in pediatric patients is reviewed because of increased evidence of unpredictable absorption and toxicity.

Administration, Topical↗