Introduction
Dengue is a mosquito-borne viral infection endemic in tropical and subtropical regions. While most infections are self-limiting, dengue hemorrhagic fever (DHF) represents a severe form characterized by increased vascular permeability, thrombocytopenia, and risk of hemorrhagic complications.
Diabetic ketoacidosis (DKA) is an acute complication of type 1 diabetes mellitus (T1DM) and is commonly encountered as the initial presentation in undiagnosed cases. It involves hyperglycemia, ketosis, and metabolic acidosis.
The concurrent occurrence of DHF and DKA is exceptionally rare but clinically significant due to overlapping symptoms such as vomiting, abdominal pain, altered sensorium, and shock-like states. The management of such cases is particularly challenging because fluid resuscitation strategies for DKA and DHF differ significantly.
Case Presentation
Patient Information:
A 10-year-old previously healthy girl was brought to the emergency department with complaints of fever for 5 days, vomiting, and abdominal pain for 3 days, and drowsiness for 1 day.
Clinical Findings:
On examination, the child was drowsy, dehydrated, tachypneic (RR 32/min), febrile (101.6°F), and hypotensive (BP 88/60 mmHg). Capillary refill time was >3 seconds, and she had cold extremities. She had no signs of bleeding, but petechiae were noted on the limbs.
Investigations:
Diagnosis:
Therapeutic Intervention:
Clinical Course:
Over the next 72 hours, the patient's metabolic parameters improved, acidosis resolved, and oral feeding was resumed. Platelet count and hematocrit normalized by day 6. She was transitioned to subcutaneous insulin and discharged in stable condition on day 8 with pediatric endocrinology follow-up.
Discussion
This case highlights a rare but clinically important scenario involving the co-occurrence of DKA and DHF. Both conditions can independently cause intravascular volume depletion and shock, but their fluid management principles diverge:
The diagnostic dilemma arises due to overlapping symptoms such as fever, vomiting, tachypnea, and abdominal pain. Laboratory findings such as hemoconcentration, thrombocytopenia, and ketonuria helped establish the dual diagnosis in this case.
In dengue-endemic areas, children presenting with DKA and fever should be evaluated for concurrent viral infections. Clinicians should tailor fluid therapy with careful titration, guided by serial clinical and laboratory parameters. Additionally, recognition of new-onset diabetes in the setting of acute febrile illness is vital.
Conclusion
Coexistence of DHF and DKA presents a critical management challenge in children. Clinicians should maintain a high index of suspicion in febrile children with metabolic acidosis, especially in dengue-endemic regions. Judicious fluid management, close monitoring, and multidisciplinary care are key to successful outcomes.
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