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dc.contributor.authorPaz-Ibarra, José
dc.contributor.authorConcepción-Zavaleta, Marcio
dc.contributor.authorQuiroz-Aldave, Juan Eduardo
dc.contributor.authorKcomt Lam, Mikaela
dc.contributor.authorHuauya, Edwars Gilvonio
dc.contributor.authorSueldo Espinoza, Diego
dc.contributor.authorGago Cajacuri, George
dc.date.accessioned2023-10-17T16:08:09Z
dc.date.available2023-10-17T16:08:09Z
dc.date.issued2023-04-09
dc.identifier.urihttps://hdl.handle.net/20.500.13053/9553
dc.description.abstract“Autoimmune dysglycemia syndrome (ADS) is a rare condition that presents as episodes of hypoglycemia as well as hyperglycemia and is classified as insulin autoimmune syndrome (IAS) and type B insulin resistance (TBIR). Autoimmunity plays a key role in the pathogenesis ofthis disorder, as evidenced by the presence of autoantibodies against endogenous insulin or the insulin receptor, and by its association with rheumatologic disorders. Treatment usually includes glycemic control and immunomodulatory agents. We report a case of a 31-year-old woman who was admitted for severe hypoglycemia. Further workup revealed underlying systemic lupus erythematosus (SLE) with renal involvement. During hospitalization, she continued to experience episodes of fasting hypoglycemia, as well as episodes of postprandial hyperglycemia. Hypoglycemia associated with a high serum insulin concentration and positive anti-insulin antibodies were consistent with IAS. Likewise, hyperglycemia and hypoglycemia in association with weight loss, acanthosis nigricans, polycystic ovarian syndrome, and normotriglyceridemia strongly suggested TBIR, although testing for antibodies against the insulin receptor was not available in Peru. Immunosuppressive therapy and metformin were indicated, resulting in remission of SLE and ADS. Years later, the patient exhibited features of dermatomyositis, such as Raynaud’s phenomenon, muscular weakness, heliotrope exanthema, and elevated muscle enzymes. Once again, the patient received immunosuppressive therapy. ADS is an infrequent cause of hypoglycemia, and the coexistence of its two pathophysiological mechanisms in a patient with SLE and subsequent development of dermatomyositis is even more rare. Our case is the first one reported describing this association.“es_PE
dc.formatapplication/pdfes_PE
dc.language.isoenges_PE
dc.publisherModestum LTDes_PE
dc.rightsinfo:eu-repo/semantics/openAccesses_PE
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/es_PE
dc.subject"hypoglycemia, hyperinsulinism, autoantibodies, systemic lupus erythematosus, dermatomyositis, autoimmune diseases"es_PE
dc.titleA rare case of autoimmune dysglycemia syndrome associated with systemic lupus erythematosus and dermatomyositises_PE
dc.typeinfo:eu-repo/semantics/articlees_PE
dc.identifier.doi10.29333/ejgm/13294"
dc.type.versioninfo:eu-repo/semantics/publishedVersiones_PE
dc.publisher.countryGBRes_PE
dc.subject.ocde3.03.00 -- Ciencias de la saludes_PE


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