We describe a man in his 30s with haemophagocytic lymphohistiocytosis (HLH), secondary to an upper respiratory tract infection, with subsequent febrile infection-related epilepsy syndrome. He had a prolonged hospital admission, during which he was treated with chemotherapy for HLH and antiepileptic medications for refractory seizures. He was discharged fully dependent to a care facility and died from aspiration pneumonia 11 months later. This case report highlights his management and discusses these conditions' pathophysiology and future management.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890756 | PMC |
http://dx.doi.org/10.1136/bcr-2022-252637 | DOI Listing |
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