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Artículo en Inglés | WPRIM | ID: wpr-188613

RESUMEN

BACKGROUND: The coexistence of an autoimmune disease and amyotrophic lateral sclerosis (ALS) has led to the hypothesis that immune-mediated pathological mechanisms are overlapping in the two diseases. We report herein a rare coexistence of bullous pemphigoid (BP) in a novel mutation (F45S) of the gene encoding Cu/Zn superoxide dismutase (SOD1) in an ALS patient, and discuss a role for the SOD1 mutation in this unusual overlap. CASE REPORT: A 57-year-old male with familial ALS, including vesicles and tense bullae on erythematous bases, was diagnosed with BP. Direct immunofluorescence revealed deposits of C3 and immunoglobulin G in the basement membrane zone. Direct sequencing of SOD1 in the patient revealed a novel mutation (c.137T>C; F45S). CONCLUSIONS: We report a novel SOD1 mutation in ALS, which was combined with BP. This novel SOD1 mutation could affect the phenotype of a combined autoimmune disease and matrix metalloproteinase-9. There may therefore be common factors linking BP and ALS with the SOD1 mutation.


Asunto(s)
Humanos , Masculino , Persona de Mediana Edad , Esclerosis Amiotrófica Lateral , Enfermedades Autoinmunes , Autoinmunidad , Membrana Basal , Técnica del Anticuerpo Fluorescente Directa , Inmunoglobulina G , Metaloproteinasa 9 de la Matriz , Penfigoide Ampolloso , Fenotipo , Superóxido Dismutasa , Estimulación Eléctrica Transcutánea del Nervio
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