ReviewFrontiers in endocrinology2026
When diabetic ketoacidosis becomes a neurological emergency: cerebral edema in a child with new-onset type 1 diabetes mellitus - a case report and narrative review.
Review in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Background: Diabetic ketoacidosis (DKA) is a life-threatening complication of type 1 diabetes mellitus (T1D), potentially leading to severe outcomes, including cerebral edema (CE). The case describes an eight-year-old child with previously undiagnosed T1D complicated by DKA, and subsequent development of CE. It is followed by a short literature review including other pediatric cases of clinically overt CE. Case presentation: A boy was admitted to the outpatient clinic with a several-day history of vomiting, abdominal pain and headache, leading to a presumptive diagnosis of gastrointestinal infection. The following day, the patient's condition deteriorated. Despite a positive family history of T1D (the patient's father), his blood glucose level was measured for the first time by the emergency medical service (25.6 mmol/L (460 mg/dL)). Further evaluation revealed DKA secondary to previously undiagnosed T1D. On admission, the boy was in severe general condition. Severe DKA was confirmed (pH 6.88), and appropriate treatment was implemented, resulting in temporary clinical stabilization. However, on the second day of hospitalization, the patient's condition deteriorated again. He was somnolent, with fluctuating consciousness and nuchal rigidity. An increase in intracranial pressure (ICP) was suspected. Optic nerve ultrasonography revealed increased optic nerve sheath diameters, also suggestive of raised ICP. Anti-edema therapy with mannitol was initiated based on clinical suspicion, resulting in clinical improvement. Dexamethasone and furosemide were administered as adjunctive therapy. Subsequent CT findings supported the diagnosis of CE. The patient was discharged after 10 days in good general condition. Conclusions: DKA can be a diagnostic challenge for clinicians due to its nonspecific symptoms. Early signs suggesting this condition should not be underestimated, and bedside blood glucose should be measured early in children presenting with unexplained vomiting, weight loss, tachypnea, dehydration or altered consciousness. Close monitoring for complications is critical during treatment, especially for CE, one of the most serious and potentially life-threatening consequences of DKA.
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