2022
DOI: 10.2337/dc21-1094
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COVID-19–Related Multisystem Inflammatory Syndrome in Children Presenting With New-Onset Type 1 Diabetes in Severe Ketoacidosis: A Case Series

Abstract: OBJECTIVE To report and describe cases of children presenting with COVID-19–related multisystem inflammatory syndrome in children (MIS-C) with new-onset type 1 diabetes mellitus (T1DM) in severe diabetic ketoacidosis (DKA). RESEARCH DESIGN AND METHODS This prospective observational study was conducted to characterize children with COVID-19–related MIS-C and new onset T1DM who were in DKA. MIS-C was diagnosed if Centers for Di… Show more

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Cited by 13 publications
(14 citation statements)
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“…New-onset diabetes in COVID-19 patients typically has an abrupt onset, severe but transient hyperglycemic episodes, and may include potentially life-threatening diabetic ketoacidosis; in this regard, it resembles T1DM more than T2DM [89]. For example, in a case series of six pediatric patients with the critical multisystem inflammatory syndrome in COVID-19, all developed diabetic ketoacidosis and were diagnosed with T1DM [90].…”
Section: New-onset Diabetesmentioning
confidence: 99%
“…New-onset diabetes in COVID-19 patients typically has an abrupt onset, severe but transient hyperglycemic episodes, and may include potentially life-threatening diabetic ketoacidosis; in this regard, it resembles T1DM more than T2DM [89]. For example, in a case series of six pediatric patients with the critical multisystem inflammatory syndrome in COVID-19, all developed diabetic ketoacidosis and were diagnosed with T1DM [90].…”
Section: New-onset Diabetesmentioning
confidence: 99%
“…The pathogenetic mechanisms of both autoinflammatory and autoimmune diseases associated with COVID-19 infection are as yet poorly understood but may involve molecular mimicry, bystander activation, and loss of immune tolerance [ 4 ]. Autoimmune endocrine conditions described following SARS-CoV-2 include type 1 diabetes [ 5 ], autoimmune thyroiditis including hypothyroidism, Graves' disease [ 6 ], and one case of autoimmune adrenalitis in an adult [ 7 ]. We report the first case of autoimmune polyglandular syndrome 2 (APS2) characterized by new-onset primary adrenal insufficiency and autoimmune primary hypothyroidism diagnosed in an adolescent, in the context of COVID-19 infection, presenting with severe systemic symptoms suggestive of MIS-C.…”
Section: Introductionmentioning
confidence: 99%
“…Following the disease definition, fever, rash, cardiac, and GIS involvement signs were reported to be the most common clinical findings of MIS-C, in several cohort studies [14,15 & ,47, [55][56][57][58]. We tried to summarize the main characteristics of MIS-C patients in Table 1 There are also other miscellaneous cases whose cardinal signs have been uncommon such as acute pancreatitis, encephalopathy, cerebellitis, diabetic ketoacidosis, hepatitis, acute appendicitis, mesenteric lymphadenopathy, ocular myasthenia, and papilledema [70][71][72][73][74][75][76][77][78]. Despite the common similarities between Kawasaki disease and MIS-C, only one MIS-C case has been reported to have erythema and induration of Bacillus Calmette-Guerin (BCG) scar so far [79].…”
Section: Clinical Featuresmentioning
confidence: 99%
“…There are also other miscellaneous cases whose cardinal signs have been uncommon such as acute pancreatitis, encephalopathy, cerebellitis, diabetic ketoacidosis, hepatitis, acute appendicitis, mesenteric lymphadenopathy, ocular myasthenia, and papilledema [70–78]. Despite the common similarities between Kawasaki disease and MIS-C, only one MIS-C case has been reported to have erythema and induration of Bacillus Calmette–Guerin (BCG) scar so far [79].…”
Section: Clinical Featuresmentioning
confidence: 99%