Sommario
Nella storia naturale delle malattie autoimmuni sono implicati diversi meccanismi autoanticorpo-mediati e/o cellulo-mediati. Nella prima parte dell’articolo vengono presi in considerazione i vari meccanismi immunopatogeni con le malattie relative. Tra questi vi è il meccanismo di tipo VII caratterizzato dalla presenza di un anticorpo che lega un ormone. Nella seconda parte di questo articolo viene presa in considerazione l’epidemiologia, l’eziopatogenesi, la fisiopatologia, le caratteristiche cliniche, immunologiche, genetiche e le implicazioni terapeutiche della sindrome di Hirata. Tale sindrome è caratterizzata da un’ipoglicemia autoimmune dovuta alla presenza di autoanticorpi anti-insulina che si formano spontaneamente o in seguito al contatto dei soggetti con farmaci con un gruppo sulfidrilico o all’acido alfa-lipoico.
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Betterle, C., Presotto, F. La sindrome di Hirata (stato dell’arte). L'Endocrinologo 17, 82–89 (2016). https://doi.org/10.1007/s40619-016-0189-7
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DOI: https://doi.org/10.1007/s40619-016-0189-7