Late-onset immune thrombocytopenia after unrelated cord blood transplantation for chronic myelomonocytic leukemia.

Blood cell therapy Pub Date : 2025-07-04 eCollection Date: 2025-08-25 DOI:10.31547/bct-2025-004
Shoya Arai, Kensuke Matsumoto, Haruko Tashiro, Seiko Kato, Takaaki Konuma, Jun Ooi
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Abstract

Several reports have been published on autoimmune hematologic complications, including immune thrombocytopenia (ITP), after cord blood transplantation (CBT). However, there have been no reports of late-onset ITP following CBT. A 51-year-old male with chronic myelomonocytic leukemia received unrelated CBT in 2012. During regular follow-up visits every 3-6 months, his complete blood count remained normal until March 2024. In September 2024, 12 years after the CBT, the patient suddenly developed severe thrombocytopenia. Following a diagnosis of ITP, the patient was treated with intravenous immunoglobulins and prednisone. With follow-up period of 5 months after the onset of ITP, the patient is still alive with a platelet count of 126 × 109/L. This case suggests that late-onset ITP after CBT occurred suddenly and may be life-threatening. Long-term follow-ups and regular clinic visits may reduce the risk of delays in diagnosis and treatment.

非相关脐带血移植后迟发性免疫性血小板减少治疗慢性髓细胞白血病。
脐带血移植(CBT)后的自身免疫性血液学并发症(包括免疫性血小板减少症(ITP))已发表了几篇报道。然而,尚无CBT后迟发性ITP的报道。一名患有慢性髓细胞白血病的51岁男性于2012年接受了无关的CBT治疗。在每3-6个月的定期随访中,他的全血细胞计数正常,直到2024年3月。2024年9月,CBT治疗12年后,患者突然出现严重的血小板减少症。诊断为ITP后,患者接受静脉注射免疫球蛋白和强的松治疗。ITP发病后随访5个月,患者仍存活,血小板计数126 × 109/L。本病例提示CBT后迟发性ITP突然发生,可能危及生命。长期随访和定期就诊可减少诊断和治疗延误的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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