DRESS (drug reaction with eosinophilia and systemic symptoms) syndrome to voxelotor treatment of sickle cell disease

Sickle cell disease (SCD), an inherited disorder, leads to polymerization of hemoglobin and formation of sickle cells resulting in vaso-occlusive crises and chronic anemia.1 Although hydroxyurea is still the most commonly used treatment, new molecules are emerging to treat sickle cell patients.2 Vox...

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Bibliographic Details
Published in:The journal of allergy and clinical immunology in practice (Cambridge, MA) Vol. 10; no. 12; pp. 3320 - 3322
Main Authors: Fargeas, Marine, Calugareanu, Andreea, Pascu, Isabela, Dupire, Gwendy, Aubineau, Magali, Cannas, Giovanna, Ben-Said, Benoit
Format: Journal Article
Language:English
Published: United States Elsevier Inc 01-12-2022
Elsevier Limited
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Summary:Sickle cell disease (SCD), an inherited disorder, leads to polymerization of hemoglobin and formation of sickle cells resulting in vaso-occlusive crises and chronic anemia.1 Although hydroxyurea is still the most commonly used treatment, new molecules are emerging to treat sickle cell patients.2 Voxelotor, was approved by the U.S. Food and Drug Administration for the SCD in 2019. Blood tests revealed lactatemia (4.5 mmol/L, N < 2.2), acute renal failure with increased creatinine level (713 μmol/L, N < 80; Figure 1, A) requiring extrarenal purification session, increased serum levels of alanine aminotransferase (×20 N), and intrahepatic cholestasis. Epstein-Barr virus, cytomegalovirus, parvovirus B19, and human herpes virus 6 blood serologies revealed an old contact, viral serologies (hepatitis B virus, hepatitis C virus, human immunodeficiency virus) as well as repeated blood cultures and antinuclear antibodies remained negative.
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ISSN:2213-2198
2213-2201
DOI:10.1016/j.jaip.2022.08.046