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  Vol. 133 No. 9, September 1997 TABLE OF CONTENTS
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Epidermolysis Bullosa Acquisita in Childhood

Claire Callot-Mellot, MD; Christine Bodemer, MD; Frederic Caux, MD; Isabelle Bourgault-Villada, MD; Sylvie Fraitag, MD; Genevìeve Goudié, MD; Martine Heller, MD; Yves de Prost, MD; Catherine Prost, MD

Arch Dermatol. 1997;133(9):1122-1126.


Abstract



Background
Epidermolysis bullosa acquisita (EBA) is an autoimmune bullous disease characterized by the presence of antitype VII collagen antibodies, leading to the formation of bullae in the dermoepidermal junction. This disease is rare in childhood.

Observations
We report 3 new cases of EBA in children. The 3 patients were similar; all 3 children were black, with a clinical phenotype resembling linear IgA bullous disease in children and typical histologic and immunologic features of EBA. In the 3 patients, diagnosis was proven using immune electron microscopy and Western blot analysis, where antitype VII collagen antibodies were demonstrated. Patients 1 and 2 were successfully treated with a combination of prednisone and dapsone. In patient 3, the lesions healed without specific therapy. We found 11 other pediatric cases of EBA in the literature and studied those cases in addition to the cases presented herein to describe the characteristics of EBA in childhood.

Conclusions
Epidermolysis bullosa aquisita is a rare disease in childhood. Mucosal involvement is frequent and severe. Because the clinical features are misleading, the use of immune electron microscopy and Western blot analysis is essential to making a diagnosis. Treatment with a combination of prednisone and dapsone is often effective. The prognosis in children is better than it is in adult patients.

Arch Dermatol. 1997;133:1122-1126



Author Affiliations



From the Departments of Dermatology (Drs Callot-Mellot, Bodemer, and de Prost) and Histopathology (Dr Fraitag), Hôpital Necker-Enfants Malades, and the Center of the Study and Diagnosis of Bullous Diseases, Hôpital Saint Louis (Drs Caux, Heller, and Prost), Paris, Dermatology Services, Hôpital Henri Mondor (Dr Bourgault-Villada), Créteil, and Hôpital Général (Dr Goudié), Dreux, France.



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Congenital Epidermolysis Bullosa Acquisita: Vertical Transfer of Maternal Autoantibody From Mother to Infant
Abrams et al.
Arch Dermatol 2011;147:337-341.
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Interventions for Mucous Membrane Pemphigoid/Cicatricial Pemphigoid and Epidermolysis Bullosa Acquisita: A Systematic Literature Review
Kirtschig et al.
Arch Dermatol 2002;138:380-384.
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