Vu Khoan, Leavitt Andrew D
Division of Hematology and Oncology, Department of Medicine, San Francisco, California.
Department of Laboratory Medicine, University of California, San Francisco, California.
Transfusion. 2018 Oct;58(10):2265-2269. doi: 10.1111/trf.14824. Epub 2018 Sep 17.
Posttransfusion purpura (PTP) is a rare condition characterized by severe thrombocytopenia following receipt of blood products. Most reported PTP cases involve alloantibodies directed against human platelet antigen (HPA)-1a. We present a case of PTP-mediated severe thrombocytopenia associated with alloantibodies directed against HPA-4a in the setting of combination checkpoint inhibitor therapy.
A 62-year-old woman with rectal melanoma that progressed on combination checkpoint inhibitors (ipilimumab and nivolumab) was admitted for abdominoperineal resection. She received multiple blood products during surgery, and between the sixth and eighth days post-surgery her platelet (PLT) count decreased from 126 × 10 /L to a nadir of 1 × 10 /L. She received intravenous immunoglobulin (IVIG), steroids, and romiplostim with eventual recovery of her PLT count to 50 × 10 /L 20 days after surgery. She tested positive for anti-HPA-4a and was shown not to express HPA-4a, confirming a diagnosis of PTP.
Alloantibodies strongly reactive to HPA-4a were detected in this patient who received multiple blood products during abdominoperineal resection surgery. Her thrombocytopenia improved with prompt administration of IVIG, steroids, and romiplostim. PTP must always be considered in patients with acute severe thrombocytopenia after receipt of blood products, and treatment should not be delayed while awaiting laboratory confirmation. To our knowledge, this is the second reported case of PTP with antibodies against HPA-4a.
输血后紫癜(PTP)是一种罕见病症,其特征为在输注血液制品后出现严重血小板减少。大多数报道的PTP病例涉及针对人类血小板抗原(HPA)-1a的同种抗体。我们报告一例在联合检查点抑制剂治疗背景下,由PTP介导的严重血小板减少,伴有针对HPA-4a的同种抗体。
一名62岁患有直肠黑色素瘤的女性,在接受联合检查点抑制剂(伊匹木单抗和纳武单抗)治疗后病情进展,因腹会阴切除术入院。她在手术期间接受了多种血液制品,术后第六天至第八天,其血小板(PLT)计数从126×10⁹/L降至最低点1×10⁹/L。她接受了静脉注射免疫球蛋白(IVIG)、类固醇和罗米司亭治疗,术后20天血小板计数最终恢复至50×10⁹/L。她抗HPA-4a检测呈阳性,且被证实不表达HPA-4a,确诊为PTP。
在该例腹会阴切除术中接受多种血液制品的患者体内检测到对HPA-4a有强烈反应的同种抗体。通过及时给予IVIG、类固醇和罗米司亭,她的血小板减少症得到改善。对于输注血液制品后出现急性严重血小板减少的患者,必须始终考虑PTP,且在等待实验室确诊期间不应延迟治疗。据我们所知,这是第二例报道的具有抗HPA-4a抗体的PTP病例。