Suppr超能文献

[患有古德综合征和新冠病毒病的患者。一例临床病例报告]

[Patient with Good's syndrome and COVID-19. Report of a clinical case].

作者信息

Maldonado-Domínguez Edwin Daniel, O Farrill-Romanillos Patricia María

机构信息

Instituto Mexicano del Seguro Social, Centro Médico Nacional Siglo XXI, Hospital de Especialidades, Departamento de Alergia e Inmunología Clínica, Clínica de Inmunodeficiencias Primarias. Ciudad de México, México.

出版信息

Rev Med Inst Mex Seguro Soc. 2022 Jul 4;60(4):474-479.

Abstract

BACKGROUND

The consequences of SARS-CoV-2 infection in patients with primary (now called "inborn errors of immunity") or secondary immunodeficiencies is still a matter of debate. There are few reports in the literature of patients with Good's syndrome and SARS-CoV-2 infection with variable outcomes.

CLINICAL CASE

A 51-year-old male with diagnosis of Good's syndrome treated with intravenous human immunoglobulin (IVIG) at a replacement dose with application every 21 days and prophylaxis for P. jirovecii with trimethoprim/ sulfamethoxazole due to profound lymphopenia at expense of T CD4+ lymphocytes who presented initially mild disease (RT-PCR+) that progressed to pneumonia with acute respiratory failure and required advanced airway management and admission to the ICU with a fatal outcome due to superinfection after 14 days hospitalized.

CONCLUSION

It has been documented in patients with humoral immunodeficiencies a better prognosis for developing less intense cytokine release syndrome. The alteration in cellular immunity, especially lymphopenia at the expense of CD4+ T lymphocytes, may be associated with a worse prognosis as the response against viruses is compromised as well as high susceptibility to superinfection by opportunistic agents such as P. aeruginosa and Mucor sp. For this reason, we must maintain close surveillance in patients with inborn errors of immunity with cellular defects, as is the case of patients with Good's syndrome who present with COVID-19.

摘要

背景

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染对原发性(现称为“先天性免疫缺陷”)或继发性免疫缺陷患者的影响仍存在争议。文献中关于古德综合征患者感染SARS-CoV-2且预后各异的报道较少。

临床病例

一名51岁男性,诊断为古德综合征,接受静脉注射人免疫球蛋白(IVIG)替代治疗,每21天应用一次,并因严重淋巴细胞减少(以CD4+T淋巴细胞减少为代价)接受甲氧苄啶/磺胺甲恶唑预防卡氏肺孢子菌感染。该患者最初表现为轻症(逆转录聚合酶链反应阳性),随后进展为肺炎并伴有急性呼吸衰竭,需要进行高级气道管理,住院14天后因二重感染入住重症监护病房,最终死亡。

结论

体液免疫缺陷患者中已有文献记载,发生强度较低的细胞因子释放综合征的预后较好。细胞免疫改变,尤其是以CD4+T淋巴细胞减少为代价的淋巴细胞减少,可能与较差的预后相关,因为对病毒的反应受到损害,同时对铜绿假单胞菌和毛霉属等机会性病原体的二重感染易感性较高。因此,我们必须对存在细胞缺陷的先天性免疫缺陷患者,如患有新型冠状病毒肺炎的古德综合征患者,进行密切监测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78f4/10395876/e4a5e7e39e35/04435117-60-4-474-c001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验