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  Vol. 123 No. 6, June 1987 TABLE OF CONTENTS
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Childhood Epidermolysis Bullosa Acquisita

Detection in a 5-Year-Old Girl

Richard Rubenstein, MD; Nancy B. Esterly, MD; Jo-David Fine, MD

Arch Dermatol. 1987;123(6):772-776.


Abstract



• A 51/2 girl with a blistering disease involving the skin and the oral, ocular, and anogenital mucosa is described. The initial clinical, histologic, and immunofluorescence findings suggested a diagnosis of cicatricial pemphigoid. However, immunoelectron microscopy demonstrated linear deposits of several immunoreactants within the sub-lamina densa region of the dermoepidermal junction, consistent with the diagnosis of epidermolysis bullosa acquisita. Although epidermolysis bullosa acquisita is considered a disease of adult onset, it should be included in the differential diagnosis of blistering diseases in children.

(Arch Dermatol 1987;123:772-776)



Author Affiliations



From the Departments of Dermatology (Drs Rubenstein and Esterly) and Pediatrics (Dr Esterly), Northwestern University Medical School, and Children's Memorial Hospital, Chicago, the Department of Dermatology, University of Alabama at Birmingham School of Medicine, and the Dermatology Section, Medical Service, Birmingham (Ala) Veterans Administration Medical Center (Dr Fine).


Footnotes



Accepted for publication Nov 27, 1986.

Reprints not available.



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Epidermolysis Bullosa Acquisita in Childhood
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Arch Dermatol 1997;133:1122-1126.
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Arch Dermatol 1991;127:373-377.
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Childhood Bullous Pemphigoid: Clinical and Immunologic Features, Treatment, and Prognosis
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Epidermolysis Bullosa Acquisita in Childhood: Differentiation From Hereditary Epidermolysis Bullosa
McCuaig et al.
Arch Dermatol 1989;125:944-949.
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