Acute chest syndrome and COVID-19 in hydroxyurea naïve sickle cell disease patient in a low resource setting.

COVID 19 SARS‐Cov‐2 acute chest syndrome case report hydroxyurea sickle cell disease

Journal

EJHaem
ISSN: 2688-6146
Titre abrégé: EJHaem
Pays: United States
ID NLM: 101761942

Informations de publication

Date de publication:
May 2022
Historique:
received: 18 01 2022
revised: 26 01 2022
accepted: 27 01 2022
pubmed: 24 5 2022
medline: 24 5 2022
entrez: 23 5 2022
Statut: epublish

Résumé

Acute chest syndrome (ACS) is a severe complication of sickle cell disease (SCD) and one of the leading causes of mortality in SCD patients. The management of ACS is challenging and requires prompt intervention to halt clinical deterioration. With the outbreak of the Coronavirus Disease 2019 (COVID-19) pandemic, which also primarily results in acute respiratory illness, the clinical picture and treatment outcome in SCD patients with ACS remain unknown. We present a case of a 30-year-old male who came in with features of painful vaso-occlusive episode and haemolysis that later evolved to acute chest syndrome. Chest X-ray showed pneumonic changes and mild bilateral pleural effusion, and nasal Reverse Transcription-Polymerase Chain Reaction (RT-PCR) for COVID-19 test came out positive. He was managed supportively with simple transfusion, antibiotics, dexamethasone and oxygen support with a good clinical outcome. Presenting with non-specific symptoms and similar respiratory symptoms and signs, the clinical picture of COVID-19 can prove difficult to discern from that of ACS due to other causes. This report emphasizes a need for a higher index of suspicion whenever a SCD patient presents with symptoms of acute respiratory distress.

Identifiants

pubmed: 35602245
doi: 10.1002/jha2.397
pii: JHA2397
pmc: PMC9110990
doi:

Types de publication

Case Reports

Langues

eng

Pagination

507-512

Informations de copyright

© 2022 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd.

Déclaration de conflit d'intérêts

The authors have no conflict of interest to disclose.

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Auteurs

William Frank Mawalla (WF)

Department of Haematology and Blood Transfusion Muhimbili University of Health and Allied Sciences Dar es Salaam Tanzania.

Ahlam Nasser (A)

Department of Haematology and Blood Transfusion Muhimbili University of Health and Allied Sciences Dar es Salaam Tanzania.

James Salumu Jingu (JS)

Department of Internal Medicine Muhimbili National Hospital Dar es Salaam Tanzania.

Happiness Joseph (H)

Department of Haematology and Blood Transfusion Muhimbili University of Health and Allied Sciences Dar es Salaam Tanzania.

Lilian Gasper Mmbaga (LG)

Department of Haematology and Blood Transfusion Muhimbili University of Health and Allied Sciences Dar es Salaam Tanzania.

Eunice Shija (E)

Department of Haematology and Blood Transfusion Muhimbili University of Health and Allied Sciences Dar es Salaam Tanzania.

Helena Kakumbula (H)

Department of Internal Medicine Muhimbili National Hospital Dar es Salaam Tanzania.

Neema Budodi Lubuva (NB)

Department of Internal Medicine Muhimbili National Hospital Dar es Salaam Tanzania.

Collins Meda (C)

Department of Internal Medicine Muhimbili National Hospital Dar es Salaam Tanzania.

Clara Chamba (C)

Department of Haematology and Blood Transfusion Muhimbili University of Health and Allied Sciences Dar es Salaam Tanzania.

Classifications MeSH