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January 23, 2026Biomedicines0 citationsOpen Access

Chronic Urticaria and Malignancy: A Review Uncovering the Common Links

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ELEralda LekliMHMehmet HoxhaMBMaria Bova

Key Points

  • This review explores the potential connections between chronic urticaria and malignancy, focusing on immune mechanisms.
  • Literature review conducted using PubMed and Google Scholar databases.
  • Studies on the relationship between chronic urticaria and malignancy were analyzed.
  • Focus on immune mechanisms and patient demographics.
  • Limited evidence exists linking chronic urticaria with malignancy.
  • Increased incidence of hematologic malignancy observed in chronic urticaria patients.
  • Certain factors like antihistamine resistance and older age may elevate malignancy risk.
  • Immunological pathways linking chronic urticaria and cancer remain poorly understood.

Abstract

Background: Chronic urticaria (CU) is a complex skin condition, frequently challenging both patients and clinicians and requiring wise individualized management. While allergy, autoimmunity, and depression are recognized comorbidities, evidence linking CU and malignancy remains underexplored. Screening for malignancy is not a routine standard of care for CU patients. Methods: A literature review was conducted to explore the potential risk or associations, including immune mechanisms, between CU and malignancy, based on searches in the PubMed and Google Scholar databases. Results: Scientific evidence on the malignancy risk in CU and its causal relationship is limited to a few population-based studies and case reports. A higher incidence of hematologic malignancy in CU patients has been reported in several publications, but the overall risk of malignancy in the CU population remains controversial. Antihistamine resistance, ultra-low IgE, and older age at the time of CU diagnosis may be related to a higher risk of malignancy, especially shortly after CU diagnosis. Immunological pathways linking CU and cancer are not clear. Immune system dysregulation, including alterations in immune checkpoints, is a feature of both cancer and CU. Such dysregulation may promote immunotolerance, abnormal immune responses, and mast cell activation through novel autoantigens and autoantibodies involved in the tumor microenvironment. Conclusions: There is growing, although limited, evidence suggesting a possible link between CU and malignancy, especially hematologic cancers. Large multicenter cohort studies are warranted to determine whether CU may act as a clinical harbinger of malignancy and to identify patient subsets that may benefit from targeted cancer screening.

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Cite This Study

Lekli et al. (2026) studied this question.

synapsesocial.com/papers/69731047c8125b09b0d1ffe3https://doi.org/10.3390/biomedicines14010229
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