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Thrombosis with Thrombocytopenia Syndrome (TTS) After ChAdOx1 nCoV-19 Immunization: An Investigative Case Report

Patient: Male, 18-year-old Final Diagnosis: Thrombosis with thrombocytopenia syndrome • probable vaccine-induced immune thrombotic thrombocytopenia Symptoms: Headache • hemiparesis • intracranial hemorrhage • thrombocytopenia • vomiting Clinical Procedure: Decompressive craniotomy • exploratory lapa...

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Detalles Bibliográficos
Autores principales: Jain, Nityanand, Chaudhary, Piyush, Shrivastava, Amit, Kaur, Taranvir, Kaur, Shabjot, Brar, Harmandeep Singh, Jindal, Ravul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037117/
https://www.ncbi.nlm.nih.gov/pubmed/36932639
http://dx.doi.org/10.12659/AJCR.938878
Descripción
Sumario:Patient: Male, 18-year-old Final Diagnosis: Thrombosis with thrombocytopenia syndrome • probable vaccine-induced immune thrombotic thrombocytopenia Symptoms: Headache • hemiparesis • intracranial hemorrhage • thrombocytopenia • vomiting Clinical Procedure: Decompressive craniotomy • exploratory laparotomy • small bowel anastomosis • IVIG administration Specialty: Surgery OBJECTIVE: Unusual clinical course BACKGROUND: Thrombosis with thrombocytopenia syndrome (TTS), including vaccine-induced immune thrombotic thrombocytopenia (VITT), is an extremely rare adverse effect, mostly seen after initial vaccination with the viral vector-based AstraZeneca-Oxford COVID-19 vaccine. It is characterized by mild to severe thrombocytopenia and venous or arterial thrombosis. CASE REPORT: Herein, we present a case of an 18-year-old male patient who developed Level 1 TTS (probable VITT) eight days after immunization with the ChADOx1 nCOV-19 vaccine (Covishield; AZ-Oxford). Initial investigations revealed severe thrombocytopenia, hemiparesis, and intracranial hemorrhage, after which the patient was treated conservatively. However, a decompressive craniotomy was performed later due to patient deterioration. One week after surgery, the patient developed bilious vomiting, lower-gastrointestinal bleeding, and abdominal distension. An abdominal CT scan was performed that showed thrombosis of the portal vein with occlusion of the left iliac vein. The patient underwent an exploratory laparotomy followed by resection and anastomosis of the small bowel due to massive gut gangrene. Due to persistent thrombocytopenia after surgery, intravenous immune globulin (IVIG) was administered. The platelet count increased thereafter, and the patient stabilized. He was discharged on the 33(rd) day after admission and was followed up for a year. No post-hospitalization complications were observed in the follow-up period. CONCLUSIONS: Although vaccines have been proven to be highly safe and effective to end the Coronavirus Disease 2019 (COVID-19) caused pandemic, there is still a small risk of developing rare complications, including TTS and VITT. Early diagnosis and prompt intervention are key for patient management.