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1.
Int J Dermatol ; 43(12): 931-5, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15569023

ABSTRACT

BACKGROUND: Cutis laxa is an uncommon entity characterized by laxity of the skin, which hangs in loose folds, producing the appearance of premature aging. It can be subdivided into congenital and acquired. This latter variant is rare and the skin involvement varies from generalized to localized. We report a case of a localized acquired cutis laxa confined to the face, without preceding inflammatory lesions or systemic compromise. Four similar cases have been reported to date. The etiology remains unknown and there is no definitive treatment. METHODS: A 27-year-old White woman came to our hospital with a wrinkled face, pendulous earlobes and drop eyelids. Changes began 5 years prior, and she appeared much older than her age. RESULTS: Histological analysis and ultrastructural examination of skin biopsy revealed reduction and fragmentation of elastic fibers, confirming the diagnosis of cutis laxa. No systemic involvement was diagnosed. The patient was submitted to plastic surgery for repair, with satisfactory results to date. CONCLUSIONS: Acquired localized cutis laxa confined to the face without preceding inflammatory lesions is extremely rare. The etiology remains unknown. Clinical features and histopathologic findings confirm the diagnosis. Surgical repair seems to be the only therapeutic choice, but the results are variable and temporary.


Subject(s)
Cutis Laxa/pathology , Facial Dermatoses/pathology , Adult , Ear Diseases/pathology , Ear, External/pathology , Elastic Tissue/pathology , Eyelid Diseases/pathology , Female , Humans
2.
Pediatr Dermatol ; 19(5): 426-31, 2002.
Article in English | MEDLINE | ID: mdl-12383101

ABSTRACT

Acrodermatitis enteropathica (AE) is a rare hereditary disorder caused by impaired absorption of zinc from the gastrointestinal tract. It is characterized by acral and periorificial dermatitis, alopecia, and diarrhea. Symptoms usually begin on weaning from breast or formula feeding. We report a full-term, 21-month-old boy with typical skin lesions and decreased plasma zinc level (12 micro g/dl). The patient was given zinc sulfate 40 mg/day and at the end of 1 month his condition had improved significantly. After reviewing the literature we emphasize the important role of zinc in human metabolism and the difference between AE and acquired zinc deficiencies.


Subject(s)
Acrodermatitis/genetics , Malabsorption Syndromes/genetics , Zinc/deficiency , Acrodermatitis/drug therapy , Acrodermatitis/etiology , Dietary Supplements , Humans , Infant , Malabsorption Syndromes/complications , Malabsorption Syndromes/drug therapy , Male , Treatment Outcome , Wound Healing/drug effects , Wound Healing/genetics , Zinc/therapeutic use
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