Un posible caso de trombocitopenia inmunitaria inducida por la vacuna contra la difteria y el tétanos

Immune thrombocytopenia (ITP) is an autoimmune disorder characterized by autoantibody-mediated platelet destruction. Vaccine-induced ITP, particularly the tetanus-diphtheria (Td) booster, is a well-documented phenomenon in children yet rare among adults. This report describes the case of a 48-year-old woman who presented with petechiae, palate and lingual bleeding, and gastrointestinal hemorrhage one week following Td booster vaccination, along with thrombocytopenia and leukocytosis. Except for uterine fibroids, she had an unremarkable medical history. Serological tests for dengue, HIV, hepatitis B, and hepatitis C, as well as a direct Coombs test, were performed to rule out alternative etiologies of ITP. An integral clinical approach and treatment with steroids and immunosuppressors, following three to four weeks, achieved clinical improvement of ITP. Previous cases and current analysis of the literature suggest molecular mechanisms and genetic factors as probable causes for this outcome; however, detailed clinical history together with environmental and clinical settings may allow for better characterization of this phenomenon.