The decedent was a 16-month-old female patient with medical history of nonaccidental trauma, sickle cell trait with trace Bart's hemoglobin, developmental delay, and premature birth at 36 weeks' gestation with uncomplicated vaginal delivery. She presented to her primary care provider with a 1-day history of fever and chills, diarrhea, and decreased appetite. She was treated with cefdinir to cover a suspected upper respiratory infection. Days later, she returned to her primary care provider with a fever of 104°F, fatigue, nasal drainage, cough, diarrhea, and decreased appetite. Chest x-ray demonstrated clear lungs, and her family was advised to continue treating with the antibiotic.The following month, she was found seizing and had a decreased level of consciousness. On admission to her local emergency department, she demonstrated marked hypoglycemia, acidemia, and thrombocytopenia. She was transferred to a tertiary medical center and was tachycardic and hypotensive on arrival. Examination revealed abdominal distention with hepatosplenomegaly. Laboratory evaluation revealed anemia and a left-shifted leukocytosis. Blood, urine, and lung cultures were negative. A respiratory viral panel detected rhinovirus/enterovirus. Further sequencing was positive for enterovirus D68. She continued to decline and died 4 days after admission.General findings at autopsy included diffuse jaundice, anasarca, and limb ischemia involving the hands and legs. Her lungs were firm and hemorrhagic on gross examination, and thrombi were visible in the small pulmonary arteries (Fig. 1). Microscopic examination of the lungs revealed pauci-septate ribbon-like hyphae, highlighted by GMS and PAS-fungus stains, invading the Manuscript