Ono Ryohei, Iwahana Togo, Aoki Kaoruko, Kato Hirotoshi, Tsutsui Yuka, Takaishi Koji, Takeda Yusuke, Sakaida Emiko, Kobayashi Yoshio
Department of Cardiovascular Medicine, Chiba University Graduate School of Medicine, Chiba, Japan.
Department of Hematology, Chiba University Graduate School of Medicine, Chiba, Japan.
J Cardiol Cases. 2024 Aug 22;30(6):181-184. doi: 10.1016/j.jccase.2024.08.003. eCollection 2024 Dec.
Immune thrombocytopenia (ITP) is an acquired autoimmune disorder characterized by low platelet counts with increased risk of bleeding. In particular, ITP induced by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has been increasingly reported. Since immunosuppressive regimens in organ transplantation are often the primary cause of increased risk of infection, ITP following solid organ transplantation has occasionally been observed. However, SARS-CoV-2 infection-induced ITP in a heart transplant patient has not been reported. We report the first case of ITP after SARS-CoV-2 infection in an orthotopic heart transplant patient who did not respond well to first-line ITP treatment. We also review the previously reported cases of SARS-CoV-2 infection-induced ITP on immunosuppressive therapy.
Post-transplant immune thrombocytopenia (ITP) may have different mechanisms than ordinal ITP; post-transplant ITP may be associated with donor condition such as history of ITP, autoantibodies, and use of immunosuppressants. Our literature review showed that severe acute respiratory syndrome coronavirus 2 infection-induced ITP patients with autoimmune diseases, with malignant hematologic disorders, or after organ transplantation may be refractory to prednisolone and intravenous immunoglobulin and require second-line ITP treatments.
免疫性血小板减少症(ITP)是一种获得性自身免疫性疾病,其特征为血小板计数低且出血风险增加。特别是,由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染引起的ITP报道日益增多。由于器官移植中的免疫抑制方案常常是感染风险增加的主要原因,实体器官移植后偶尔会观察到ITP。然而,尚未有心脏移植患者发生SARS-CoV-2感染诱导的ITP的报道。我们报告了首例原位心脏移植患者在感染SARS-CoV-2后发生ITP且对一线ITP治疗反应不佳的病例。我们还回顾了先前报道的接受免疫抑制治疗的SARS-CoV-2感染诱导的ITP病例。
移植后免疫性血小板减少症(ITP)可能具有与普通ITP不同的机制;移植后ITP可能与供体状况有关,如ITP病史、自身抗体以及免疫抑制剂的使用。我们的文献综述表明,严重急性呼吸综合征冠状病毒2感染诱导的ITP患者,若患有自身免疫性疾病、恶性血液系统疾病或在器官移植后,可能对泼尼松龙和静脉注射免疫球蛋白难治,需要二线ITP治疗。