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Epidermolysis Bullosa Acquisita With Negative Direct Immunofluorescence
Jean-Philippe Lacour, MD;
Lennart Juhlin, MD;
Philip El Baze, MD;
Jean-Paul Ortonne, MD
Arch Dermatol. 1985;121(9):1183-1185.
Abstract
Epidermolysis bullosa (EB) appeared in a patient at the age of 54 years. Other bullous disorders could be excluded by electron microscopy, and there was no family history of EB. The patient would therefore best be classified as having EB acquisita. Repeated direct immunofluorescence studies were, however, negative for all tested serum samples, suggesting that there might be a subgroup lacking immunoglobulin deposits in the skin. Collagen IV, laminin, and fibronectin were expressed normally at the dermoepidermal junction.
(Arch Dermatol 1985;121:1183-1185)
Author Affiliations
From the Dermatology Service, Pasteur Hospital, Nice, France. Dr Juhlin was a visiting professor at the time of the study; he is now with the Department of Dermatology, University of Uppsala, Sweden.
Footnotes
Accepted for publication Feb 5, 1985.
Reprint requests to Service de Dermatologie, Hôpital Pasteur, 30 Avenue Voie Romaine, 06002 Nice Cedex, France (Dr Ortonne).
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