Cerebral fat embolism syndrome in a patient with homozygous sickle cell disease in the setting of multisystem inflammatory syndrome in children.

Autor: Sepulveda K; Department of Pediatrics, Baylor Scott & White McLane Children's Medical Center, Temple, Texas., Issa T; Department of Pediatrics, Baylor Scott & White McLane Children's Medical Center, Temple, Texas., Dubrocq G; Department of Pediatrics, Baylor Scott & White McLane Children's Medical Center, Temple, Texas.
Jazyk: angličtina
Zdroj: Proceedings (Baylor University. Medical Center) [Proc (Bayl Univ Med Cent)] 2022 Dec 20; Vol. 36 (2), pp. 266-268. Date of Electronic Publication: 2022 Dec 20 (Print Publication: 2023).
DOI: 10.1080/08998280.2022.2155927
Abstrakt: Multisystem inflammatory syndrome in children (MIS-C) is a rare progressive inflammatory process temporally associated with exposure to SARS-CoV-2 (COVID-19) in patients 20 years of age and younger. At this time, much of MIS-C is not well understood, including the pathogenesis, long-term implications, and how each variant of the COVID-19 virus affects the progression and severity. We present the unusual case of a 19-year-old man with a history of homozygous sickle cell disease who developed a vaso-occlusive pain crisis and cerebral fat embolism syndrome as a complication of MIS-C secondary to the Omicron variant of COVID-19.
Competing Interests: The authors report no funding or conflicts of interest. The patient and family have consented to the publication of this case.
(Copyright © 2022 Baylor University Medical Center.)
Databáze: MEDLINE