Drug-induced hypersensitivity syndrome induced by propylthiouracil: case report and literature review
- PMID: 35933436
- PMCID: PMC9357314
- DOI: 10.1186/s13223-022-00707-w
Drug-induced hypersensitivity syndrome induced by propylthiouracil: case report and literature review
Abstract
Background: Drug-induced hypersensitivity syndrome (DIHS) is a rare, potentially life-threatening systemic drug reaction. Antithyroid drugs (ATDs) causing DIHS have seldom been reported before.
Case presentation: We present a case of propylthiouracil (PTU)-induced DIHS, which included fever, skin rash, lymphadenopathy, hepatosplenomegaly, serious liver and kidney dysfunction, peripheral blood eosinophilia, and atypical lymphocytosis. Following supportive therapy, intravenous immunoglobulin (IVIG), and systemic corticosteroid, the patient experienced a resolution of fever and rash combined with progressive normalization of hematological index and organ function. These clinical features, and the skin lesion biopsy confirmed DIHS diagnosis.
Conclusions: To our knowledge, this is the second reported case of PTU-induced DIHS worldwide and the first human leukocyte antigen (HLA) typing of PTU-induced DIHS. Clinicians should cautiously distinguish hyperthyroidism etiology and identify the indication of ATDs. Timely recognition and formal DIHS treatment are required in patients with ATDs.
Keywords: Drug-induced hypersensitivity syndrome; Human leukocyte antigen; Propylthiouracil.
© 2022. The Author(s).
Conflict of interest statement
The authors declare no competing interests.
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References
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- Kardaun SH, Sekula P, Valeyrie-Allanore L, Liss Y, Chu CY, Creamer D, et al. Drug reaction with eosinophilia and systemic symptoms (DRESS): an original multisystem adverse drug reaction. Results from the prospective RegiSCAR study. Br J Dermatol. 2013;169:1071–1080. doi: 10.1111/bjd.12501. - DOI - PubMed
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