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Childhood pemphigus vulgaris is a challenging diagnosis
Lins Filho, Gastão Tenório; Barbosa, Nathalia Lages Sarmento; Abreu, Eulina Maria Vieira de; Costa, Klinger Vagner Teixeira da; Meneses, Kelly Chrystine Barbosa; Silva, Rodrigo Neves; Ferreira, Sonia Maria Soares.
Afiliación
  • Lins Filho, Gastão Tenório; Centro Universitário CESMAC. Curso de Odontologia. Maceió. BR
  • Barbosa, Nathalia Lages Sarmento; Centro Universitário CESMAC. Curso de Odontologia. Maceió. BR
  • Abreu, Eulina Maria Vieira de; Posto de Atendimento Médico Salgadinho-Serviço de Dermatologia. Maceió. BR
  • Costa, Klinger Vagner Teixeira da; Centro Universitário CESMAC. Curso de Medicina. Maceió. BR
  • Meneses, Kelly Chrystine Barbosa; Centro Universitário CESMAC. Curso de Medicina. Maceió. BR
  • Silva, Rodrigo Neves; Centro Universitário CESMAC. Curso de Odontologia. Maceió. BR
  • Ferreira, Sonia Maria Soares; Centro Universitário CESMAC. Curso de Odontologia. Maceió. BR
Autops. Case Rep ; 11: e2021267, 2021. graf
Article en En | LILACS | ID: biblio-1249009
Biblioteca responsable: BR26.7
ABSTRACT
Pemphigus Vulgaris (PV) is an uncommon autoimmune and blistering mucocutaneous disease. Childhood Pemphigus Vulgaris (CPV) is a pediatric variant of PV, which affects children below 12 years, being very rare among children under 10 years of age. CPV has similar clinical, histological, and immunological features as seen in PV in adults. The mucocutaneous clinical presentation is the most common in both age groups. Vesicles and erosions arising from the disease usually cause pain. A few CPV cases have been reported in the literature. This study reports a case of an 8-year-old male patient with oral lesions since the age of 3 years, and the diagnosis of pemphigus was achieved only 2 years after the appearance of the initial lesions. CPV remains a rare disease, making the diagnosis of this clinical case a challenge due to its age of onset and clinical features presented by the patient. Therefore, dentists and physicians should know how to differentiate CPV from other bullous autoimmune diseases more common in childhood.
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Texto completo: 1 Índice: LILACS Asunto principal: Pénfigo Tipo de estudio: Diagnostic_studies Límite: Child / Humans / Male Idioma: En Revista: Autops. Case Rep Asunto de la revista: Anatomia / Patologia Cl¡nica / Patologia Legal Año: 2021 Tipo del documento: Article

Texto completo: 1 Índice: LILACS Asunto principal: Pénfigo Tipo de estudio: Diagnostic_studies Límite: Child / Humans / Male Idioma: En Revista: Autops. Case Rep Asunto de la revista: Anatomia / Patologia Cl¡nica / Patologia Legal Año: 2021 Tipo del documento: Article