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2.
J Am Acad Dermatol ; 40(5 Pt 1): 649-71; quiz 672-3, 1999 May.
Article in English | MEDLINE | ID: mdl-10321591

ABSTRACT

Pemphigus describes a group of autoimmune diseases characterized by blisters and erosions of the skin and mucous membranes, acantholysis by histology, and autoantibodies directed against epidermal cell surface components. Since the early 1970s, the following new clinical variants of pemphigus have been reported: pemphigus herpetiformis, IgA pemphigus, and paraneoplastic pemphigus. In recent years, significant data have been obtained from laboratory investigation on these rare and atypical variants, especially regarding their specific target antigens. We review these variants, their clinical presentations, histologic findings, immunopathology, target antigens, theories of pathogenesis, treatment modalities, and clinical courses.


Subject(s)
Pemphigus/classification , Acantholysis/pathology , Autoantibodies/immunology , Autoantigens/analysis , Autoimmune Diseases/classification , Blister/pathology , Dermatitis Herpetiformis/classification , Epidermis/immunology , Humans , Immunoglobulin A/immunology , Paraneoplastic Syndromes/classification , Paraneoplastic Syndromes/immunology , Pemphigus/immunology , Pemphigus/pathology , Prognosis
3.
Dermatologica ; 178(4): 181-3, 1989.
Article in English | MEDLINE | ID: mdl-2670617

ABSTRACT

The term polymorphic pemphigoid has been used in the literature as a variant of bullous pemphigoid. But this term is imprecise and now obsolete, since patients with linear IgA dermatosis have been reported under this terminology. The patients who develop an atypical subepidermal bullous disease with clinical and histological features of both bullous pemphigoid and dermatitis herpetiformis may actually be classified into three groups: (1) vesicular variant of bullous pemphigoid; (2) linear IgA dermatosis, and (3) mixed subepidermal bullous disease.


Subject(s)
Pemphigoid, Bullous/classification , Skin Diseases, Vesiculobullous/classification , Terminology as Topic , Dermatitis Herpetiformis/classification , Humans , Immunoglobulin A/immunology , Skin Diseases, Vesiculobullous/immunology
14.
Fontilles, Rev. leprol ; 7(2): 229-232, Jul.-Dic. 1968. ilus
Article in Spanish | Sec. Est. Saúde SP, HANSEN, Hanseníase Leprosy, SESSP-ILSLACERVO, Sec. Est. Saúde SP | ID: biblio-1226135

ABSTRACT

Tres de entre 40 enfermos del Mal de Hansen que fueran tratados con talidomida, desde noviembre de 1964 hasta la fecha, evidenciaron lesiones vesiculares. El examen histopatológico practicado en 2 de éstos mostró un cuadro semejante a la dermatitis herpertiforme. La anamnesis, la evolución y el diagnóstico diferencial permiten suponer que se trata de manifestaciones originadas en el tratamiento con talidomida.


Subject(s)
Dermatitis Herpetiformis/classification , Dermatitis Herpetiformis/diagnosis , Dermatitis Herpetiformis/prevention & control , Dermatitis Herpetiformis/drug therapy , Leprosy , Leprosy/classification , Leprosy/diagnosis , Leprosy/drug therapy
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