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June 3, 2026The Journal of Rheumatology0 citations

Hydroxychloroquine Sulfate-Associated Skin Lesions: Clinical Features and Mechanisms

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LYLi YangXLXiang LiQZQinghua Zou

Key Points

  • This review aims to characterize the clinical features and mechanisms of skin lesions caused by hydroxychloroquine, focusing on adverse reactions.
  • Searched databases including PubMed, Web of Science, Embase, and Cochrane Library up to December 2025.
  • Included original studies, reviews, and case reports on hydroxychloroquine and skin lesions, assessing study quality.
  • Two reviewers screened literature independently to ensure data completeness and rigor.
  • Common adverse reactions include pigmentation, maculopapular rash, and pruritus; severe reactions include AGEP, DRESS, SJS, and TEN.
  • Mechanisms involve alteration of pigment metabolism and lysosomal ion trapping, along with immune hypersensitivity.
  • Management strategies include dose adjustment, drug discontinuation, and desensitization for select mild cases.

Abstract

Hydroxychloroquine (HCQ) is pivotal in rheumatology and dermatology for its potent anti-malarial and immunomodulatory properties. Though generally safe, HCQ causes cutaneous adverse reactions (CARs) ranging from mild pigmentation to life-threatening severe cutaneous adverse reactions (SCARs). This review synthesizes data from studies indexed PubMed, Web of Science, Embase, and the Cochrane Library up to December 2025. Search keywords included "hydroxychloroquine," "adverse reactions," "skin lesions" (e.g., pigmentation, maculopapular rash, psoriasiform eruption), and "mechanisms." We included original studies, reviews, and case reports, excluding duplicates and studies focused solely on non-cutaneous reactions. Two reviewers independently screened the literature, and any discrepancies were resolved via discussion. Study quality was assessed based on methodological rigor and data completeness, with priority given to high‑impact literature published in the last decade.Common adverse reactions include pigmentation, maculopapular rash, and pruritus; rare but severe reactions include acute generalized exanthematous pustulosis (AGEP), drug hypersensitivity syndrome (DRESS), Stevens-Johnson syndrome (SJS), and toxic epidermal necrolysis (TEN). Underlying mechanisms may involve alteration of pigment metabolism, lysosomal ion trapping, and T-cell-mediated hypersensitivity. Management depends on early recognition, dose adjustment, or drug discontinuation. For select mild cases, desensitization may be appropriate. Ongoing monitoring of pharmacovigilance databases is crucial for proactive surveillance and early warning.

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Cite This Study

Yang et al. (2026) studied this question.

synapsesocial.com/papers/6a1fc76ddee9eb8c0dce85c4https://doi.org/10.3899/jrheum.2025-1087
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