Detalhes do Documento

Diagnostic Challenge in a Sickle Cell Disease Patient with COVID-19

Autor(es): Rodrigues, J ; Silva, TM ; Garcia, AM ; Soares, E ; Brito, MJ

Data: 2022

Identificador Persistente: http://hdl.handle.net/10400.17/4280

Origem: Repositório do Centro Hospitalar de Lisboa Central, EPE

Assunto(s): Acute Chest Syndrome/diagnosis; Acute Chest Syndrome/diagnostic imaging; Acute Chest Syndrome/therapy; Anemia, Sickle Cell/ complications; COVID-19/complications; Diagnosis, Differential; SARS-CoV-2; Tomography, X-ray Computed; Adolescent; HDE IMA; HDE INF PED


Descrição

Acute chest syndrome is a life-threatening complication in sickle cell disease. Infections are frequently implied, and like other viruses, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) may be a trigger. In addition, due to their inflammatory status, they may present a higher risk for severe coronavirus disease 2019 (COVID-19). Pneumonia and acute chest syndrome share clinical, laboratory, and radiological features and may overlap, which makes their differential diagnosis especially challenging. We describe a case of an adolescent with homozygous sickle cell disease that developed acute chest syndrome in the context of COVID-19. With it, we intend to bring awareness to the potential role of imaging in the differential diagnosis and in establishing the best approach for the patient. Chest computed tomography findings were suggestive of an alternative diagnosis to COVID-19 pneumonia and red cell transfusion, fluid management, analgesics, and antibiotics were administered with favorable outcome.

Tipo de Documento Artigo científico
Idioma Inglês
Contribuidor(es) Repositório da Unidade Local de Saúde São José
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