Clinical Observation of COVID-19 in a Patient With an Acquired Humoral Deficiency Secondary to Chemotherapeutic Agents

被引:2
作者
Schend, Jason [1 ]
Daniels, Phuong [2 ]
Sanan, Neha [1 ]
Tcheurekdjian, Haig [1 ,3 ]
Hostoffer, Robert [1 ,2 ,3 ]
机构
[1] Univ Hosp Cleveland, Med Ctr, Dept Pulm Crit Care, Cleveland, OH 44106 USA
[2] Lake Erie Coll Osteopath Med, Dept Pediat, Erie, PA USA
[3] Allergy Immunol Assoc Inc, Mayfield Hts, OH USA
来源
ALLERGY & RHINOLOGY | 2020年 / 11卷
关键词
COVID-19; immunodeficiency; rituximab; SARS-CoV-2; chemotherapy; CORONAVIRUS DISEASE 2019;
D O I
10.1177/2152656720978764
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Introduction: The coronavirus disease 2019 (COVID-19) pandemic due to the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes worldwide devastation. We describe the course of a patient with COVID-19 in the setting of an acquired humoral deficiency as a result of chemotherapeutic treatment for rheumatologic conditions. Case Report: A 49-year-old Caucasian male presented with non-relieving fever, hypoxemia, and persistent diarrhea after seven days following a positive SARS-CoV-2 polymerase chain reaction (PCR) assay. The patient's past medical history was significant for mixed connective tissue disease, rheumatoid arthritis, and systemic lupus erythematosus treated with methotrexate and rituximab since 2008. He was diagnosed with acquired humoral deficiency in 2017 managed by intravenous immunoglobulin (IVIG) infusion every three weeks. The patient's course of hospitalization was complicated by acute respiratory distress which necessitated intensive unit care and required up to 20 L/min oxygen supplementation via a humidified high flow generator. He was treated with hydroxychloroquine and azithromycin and received an IVIG transfusion. The patient was discharged to home after forty-two days of hospitalization with oxygen supplementation only during ambulation and a complete resolution of diarrhea. Discussion: According to current limited data, patients with immunodeficiency have longer length of hospitalization compared to immunocompetent individuals. Our patient demonstrated a form of immunodeficiency as the result of a chemotherapeutic agent, and his clinical course appeared to be more severe. Conclusion: More studies are necessary to shed light on the immunological response to SARS-CoV-2 and its impact on immunocompromised and immunocompetent and individuals. We describe the course of a patient with COVID-19 in the setting of an acquired humoral deficiency.
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