Pessoa Natália Lima, Diniz Lilian Martins Oliveira, Andrade Adriana de Souza, Kroon Erna Geessien, Bentes Aline Almeida, Campos Marco Antônio
Laboratório de Vírus Departamento de Microbiologia Instituto de Ciências Biológicas Universidade Federal de Minas Gerais Belo Horizonte Brazil.
Imunologia de Doenças Virais, Instituto René Rachou Fundação Oswaldo Cruz Belo Horizonte Brazil.
EJHaem. 2021 Nov 24;3(1):199-202. doi: 10.1002/jha2.325. eCollection 2022 Feb.
Here we report three clinical cases of children with sickle cell disease (SCD) and severe COVID-19 who evolved with complications during hospitalization or after discharge. They present single nucleotide polymorphisms in and genes, identified from 37 patients under 16 years old hospitalized from September 2020 to May 2021 in the Hospital João Paulo II, Belo Horizonte, Brazil. They presented significant complications of SCD as acute chest syndrome, splenic sequestration, and pain crisis during hospitalization or up to 2 months after SARS-CoV-2 infection. They all required transfusion of concentrated red blood cells and hospitalization in a reference hospital to care for children with SCD.
在此,我们报告三例镰状细胞病(SCD)患儿合并重症 COVID-19 的临床病例,这些患儿在住院期间或出院后出现了并发症。他们存在 和 基因的单核苷酸多态性,这些是从 2020 年 9 月至 2021 年 5 月在巴西贝洛奥里藏特的若昂·保罗二世医院住院的 37 名 16 岁以下患者中鉴定出来的。他们在住院期间或感染 SARS-CoV-2 后长达 2 个月出现了 SCD 的严重并发症,如急性胸综合征、脾隔离症和疼痛危象。他们都需要输注浓缩红细胞,并在一家参考医院住院,以照顾患有 SCD 的儿童。