1989
DOI: 10.1016/s0190-9622(89)70079-7
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Endemic pemphigus foliaceus (fogo seivagem). I. Clinical features and immunopathology

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Cited by 159 publications
(115 citation statements)
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“…Endemic pemphigus foliaceus (EPF) is an autoimmune blistering skin disease presenting in well-defined geographic regions [1][2][3][4][5][6][7]. The roles of IgG autoantibodies and complement in lesional EPF skin has been previously documented [1][2][3][4][5][6][7].…”
Section: Introductionmentioning
confidence: 99%
“…Endemic pemphigus foliaceus (EPF) is an autoimmune blistering skin disease presenting in well-defined geographic regions [1][2][3][4][5][6][7]. The roles of IgG autoantibodies and complement in lesional EPF skin has been previously documented [1][2][3][4][5][6][7].…”
Section: Introductionmentioning
confidence: 99%
“…Trata-se de Sinal clássico, bem caracterizado em casos de pênfigo foliáceo humano, na modalidade endêmi-ca ("pênfigo brasileiro" ou "sul-americano" ou, ainda, fogo-selvagem) (DIAZ et al, 1989;FURTADO, 1959). Foi referido, de forma magistral, por Vieira (1948), dermatologista brasileiro, na fase de evolução para a cura da enfermidade, denominada "aurora da cura".…”
Section: Salpico De Lamaunclassified
“…Canino penfigoso no pós-terapia Fonte: (LARSSON, 2014) Figura 27 -Pênfigo foliáceo -lesões ventrais, na pré-terapia de pênfigo foliáceo canino. Aspecto pustular erosado (configuração circinada) disseminado em área abdominal ventral e úmero-radio-ulnar (canino da figura 26) Fonte: (LARSSON, 2014) Histologicamente, há proliferação melanocítica intraepidérmica e consequente aumento da deposição melânica, incontinência pigmentar com acúmulo de melanina nos fagócitos dérmicos (DIAZ et al, 1989).…”
Section: Salpico De Lamaunclassified
“…3) (Eyre and Stanley, 1988). It is still a paradox, therefore, that pemphigus vulgaris antibodies, in spite of their broader binding capacity, cause loss of cell adhesion at only the suprabasal level, and that pemphigus foliaceus patients, in whom mucosal lesions rarely occur, show in vivo-bound autoantibodies in oral and esophageal mucosa (Diaz et al, 1989). The recent demonstration of antibodies to desmosomal plaque proteins in both pemphigus vulgaris and pemphigus foleaceus patients, however, may explain these staining patterns The intercellular localization of this antigen (from 180 to 190 kDa) does not favor inclusion of anti-180-to 190-kDa antibodies among pathogenic pemphigus autoantibodies, but they will nevertheless produce staining in indirect immunofluorescence staining (loly et al, 1994 (Rock et al, 1989;Allen et al, 1993;Calvanico et al, 1993;Bhol et al, 1995).…”
Section: Immunopathologymentioning
confidence: 99%