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Immunostimulatory Agent Evaluation: Lymphoid Tissue Extraction and Injection Route-Dependent Dendritic Cell Activation
Published on: September 16, 2018
Cutaneous Lymphomas and Lymphoproliferative Disorders Associated With SARS-CoV-2 Vaccination: A Systematic Review
Martina Mussi1,2, Corrado Zengarini1,2, Alberto Corrà3
1Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy, unibo.it.
COVID-19 vaccination is linked to rare cutaneous lymphomas (CLs) and non-neoplastic lymphoproliferative disorders (nn-LPDs). While a causal link is unproven, the short onset time suggests vaccination may trigger existing conditions, necessitating pharmacovigilance.
Area of Science:
- Dermatology
- Oncology
- Immunology
Background:
- Cutaneous lymphomas (CLs) are rare T-cell skin cancers.
- Post-SARS-CoV-2 vaccination reports suggest potential links to CLs and non-neoplastic lymphoproliferative disorders (nn-LPDs).
Purpose of the Study:
- To systematically review literature on CLs and nn-LPDs following COVID-19 vaccination.
- Analyze clinical features, subtypes, onset latency, and potential mechanisms.
Main Methods:
- Systematic review adhering to PRISMA guidelines.
- Inclusion of case reports/series of new-onset or relapsed CLs/nn-LPDs post-vaccination.
- Extraction and analysis of demographic, clinical, histological, therapeutic, and temporal data.
Main Results:
- 35 cases identified across 15 manuscripts.
- 51.4% were confirmed CLs (e.g., lymphomatoid papulosis, Sézary syndrome, mycosis fungoides).
- 48.6% were nn-LPDs; 76.2% showed CD30 positivity; 80% received Pfizer-BioNTech vaccine; new-onset CLs appeared within 3-42 days (median 14 days).
Conclusions:
- Most cases involved low-grade T-cell CLs and nn-LPDs.
- Short latency suggests vaccination may trigger underlying conditions, highlighting the need for pharmacovigilance.
- These rare events do not negatively impact the overall favorable risk-benefit of COVID-19 vaccination.
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