STAT5b gain-of-function disease in a child with mycobacterial osteomyelitis of the skull: rare presentation of an emerging disease entity.
Andrew J KobetsSamuel AhmadAndre BoykeDavid OrikoRyan HollandRachel EisenbergSeyed Ahmad Naseri AlaviRick AbbottPublished in: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery (2023)
Patients with STAT5b gain-of-function mutations have attenuated Th1 responses and are treated with medications, such as JAK inhibitors, which further inhibit other STAT proteins that regulate immunity against rare infectious entities, such as mycobacterium. Our case highlights the importance of considering these rare infections in patients on JAK inhibitors and with STAT protein mutations. Possessing a clear mechanistic understanding of this genetic mutation, its downstream effect, and the consequences of treatment may enhance a physician's diagnostic and clinical management of similar patients in the future.