AI Article Synopsis

  • Countries are focusing on vaccinating populations against COVID-19 to prevent severe disease, hospitalizations, and healthcare strain as new variants emerge.
  • There is increasing evidence of rare side effects from COVID-19 vaccines, including IgA vasculitis, a condition characterized by visible skin symptoms and various systemic issues.
  • A case study is presented involving a 72-year-old patient who developed IgA vasculitis symptoms two weeks after receiving the Pfizer BioNTech vaccine, with lab results confirming the diagnosis as a potential vaccine-related side effect.

Article Abstract

As new variants of SARS-CoV-2 continue to emerge worldwide, countries are striving to fully vaccinate their population in a bid to prevent severe disease, subsequent hospitalizations, and the associated strain on their healthcare systems and death. In this context, there is growing evidence of rare, potential side effects associated with COVID-19 vaccines. IgA vasculitis is a systemic, IgA-mediated vasculitis characterized by palpable purpura, arthralgia, abdominal pain, and renal involvement. It is the most common type of vasculitis in childhood, sporadically affecting the adult population. However, there have been multiple reports of IgA vasculitis following vaccination against COVID-19. Herein, we present the case of a 72-year-old patient with palpable purpura that developed two weeks after receiving the Pfizer BioNTech vaccine. Laboratory investigations revealed elevated serum creatinine (2.6 mg/dL), macroalbuminuria (8.6 g/24 h), and macroscopic hematuria. Histopathological examination confirmed necrotizing vasculitis, and a diagnosis of IgA vasculitis was established. Considering the clinical presentation, the laboratory and histopathological findings, and the time interval between the vaccination and the development of symptoms, we strongly believe that IgA vasculitis in this patient arose as a side effect of the Pfizer BioNTech vaccine.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9937717PMC
http://dx.doi.org/10.7759/cureus.33938DOI Listing

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