1978
DOI: 10.1111/j.1365-2230.1978.tb01474.x
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Eosinophilic spongiosis: a localized bullous dermatosis unassociated with pemphigus

Abstract: Summary Two women with recurrent, localized, bullous eruptions showing the histological changes of eosinophilic spongiosis are described. The natural history, and the absence of immunopathological evidence of pemphigus, distinguishes these cases from those described as a variant of pemphigus. They appear to form a separate, as yet unclassifiable, subgroup.

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Cited by 4 publications
(1 citation statement)
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“…Other variants of pemphigus, such as eosinophilic spongiosis, may be more difficult to identify since these cases may clinically resemble bullous pemphigoid or dermatitis herpetiformis. Immunopathologicaily the majority of cases of eosinophilic spongiosis can be shown to belong to the pemphigus group with intercellular epidermal direct IMF (Knight, Black & Delaney, 1976), although there are other cases who appear to be unrelated to pemphigus (Knight et al, 1976;Black 1977;Kennedy, Hodge & Sanderson, 1978). ' I 2.…”
Section: Imf Findings In the Bullous Disordersmentioning
confidence: 99%
“…Other variants of pemphigus, such as eosinophilic spongiosis, may be more difficult to identify since these cases may clinically resemble bullous pemphigoid or dermatitis herpetiformis. Immunopathologicaily the majority of cases of eosinophilic spongiosis can be shown to belong to the pemphigus group with intercellular epidermal direct IMF (Knight, Black & Delaney, 1976), although there are other cases who appear to be unrelated to pemphigus (Knight et al, 1976;Black 1977;Kennedy, Hodge & Sanderson, 1978). ' I 2.…”
Section: Imf Findings In the Bullous Disordersmentioning
confidence: 99%