Tews Hauke Christian, Driendl Sarah M, Kandulski Melanie, Buechler Christa, Heiss Peter, Stöckert Petra, Heissner Klaus, Paulus Michael G, Kunst Claudia, Müller Martina, Schmid Stephan
Department of Internal Medicine I, Gastroenterology, Hepatology, Endocrinology, Rheumatology and Infectious Diseases, University Hospital Regensburg, Franz-Josef-Strauss-Allee 11, 93053 Regensburg, Germany.
Department of Radiology, University Hospital Regensburg, University Hospital Regensburg, Franz-Josef-Strauss-Allee 11, 93053 Regensburg, Germany.
Vaccines (Basel). 2022 Apr 12;10(4):595. doi: 10.3390/vaccines10040595.
Vaccine-induced immune thrombotic thrombocytopenia (VITT) with venous thrombosis is a rare complication of SARS-CoV-2 vaccination with ChAdOx1 (AstraZeneca) and AD26.COV2.S (Johnson & Johnson, New Brunswick, NJ, USA) associated with high mortality. At present, there are no known differences in the pathophysiology or risk factors of VITT with the AstraZeneca vaccine (ChAdOx1) compared with the Johnson & Johnson vaccine (AD26.COV2.S). Herein, we present the case of a healthy 39-year-old patient with VITT after having received the vaccine Ad26.COV2.S. Ten days after vaccination, the patient developed a deep vein thrombosis and subsequent pulmonary embolism. A computed tomography scan of the abdomen showed adrenal gland bleeding and an adrenocorticotrophic hormone stimulation test diagnosed adrenal insufficiency. Therapy with intravenous immunoglobulin, argatroban and hydrocortisone was initiated immediately after diagnosis. The patient left the hospital 22 days after admission with the diagnosis of adrenal insufficiency but otherwise in good health. To the best of our knowledge, five cases of VITT and adrenal bleeding have been described to date in the literature but the presented case was the first to occur after immunisation with the vaccine of Johnson & Johnson. In summary, VITT-associated adrenal dysfunction is a very rare complication of vaccination with an adenoviral vector-based COVID-19 vaccine.
疫苗诱导的免疫性血栓性血小板减少症(VITT)伴静脉血栓形成是接种阿斯利康公司的ChAdOx1疫苗和美国新泽西州强生公司的AD26.COV2.S疫苗后出现的一种罕见并发症,死亡率很高。目前,与强生疫苗(AD26.COV2.S)相比,阿斯利康疫苗(ChAdOx1)引起的VITT在病理生理学或风险因素方面尚无已知差异。在此,我们报告一例39岁健康患者在接种AD26.COV2.S疫苗后发生VITT的病例。接种疫苗10天后,患者出现深静脉血栓形成及随后的肺栓塞。腹部计算机断层扫描显示肾上腺出血,促肾上腺皮质激素刺激试验诊断为肾上腺功能不全。诊断后立即开始静脉注射免疫球蛋白、阿加曲班和氢化可的松治疗。患者入院22天后出院,诊断为肾上腺功能不全,但其他方面健康状况良好。据我们所知,迄今为止文献中已描述了5例VITT和肾上腺出血病例,但本病例是首例在接种强生疫苗后发生的。总之,VITT相关的肾上腺功能障碍是基于腺病毒载体的COVID-19疫苗接种非常罕见的并发症。