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. |
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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 |
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