紧急脾栓塞治疗难治性免疫性血小板减少症合并重症出血1例。

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL
AME Case Reports Pub Date : 2025-07-15 eCollection Date: 2025-01-01 DOI:10.21037/acr-25-25
Hayabusa Takano, Naoki Hara, Eri Nakajima, Kouhei Katsuda, Kenki Usami, Ayaka Hasegawa, Jun Matsuda, Satoshi Arino, Nobuo Sasaki, Naoki Kojima, Hiroshi Inagawa, Yasusei Okada, Akira Fujita
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引用次数: 0

摘要

背景:免疫性血小板减少症(ITP)的特点是由于免疫机制导致血小板计数减少。一线治疗是皮质类固醇,血栓生成素受体激动剂、利妥昔单抗和脾切除术作为二线选择。虽然手术脾切除术是有效的,但严重血小板减少患者出血风险高。脾栓塞(SE)被认为是治疗类固醇难治性慢性ITP的一种替代脾切除术的方法,据报道是一种有效且微创的选择。然而,对于急性ITP伴有危及生命的出血,很少有SE的报道。病例描述:一名63岁男性,因口腔出血、便血和复发性晕厥而休克。实验室检查显示严重的血小板减少(4000 /mm3血小板)和血小板相关免疫球蛋白G (PA-IgG)升高,导致ITP诊断。尽管输了血小板、静脉注射免疫球蛋白和大剂量类固醇,他的病情仍恶化,第3天出现肺泡出血。考虑到手术风险,在第5天使用线圈和明胶海绵进行紧急SE。在给予SE和血小板生成素受体激动剂后,血小板计数从第6天开始改善,可以在第11天停止输血。患者于第12天从重症监护病房出院,血小板稳定,呼吸状况改善。结论:该病例表明,对于难治性ITP伴有危及生命的出血,特别是当严重的血小板减少症使手术无法干预时,紧急SE是一种有效和安全的脾切除术替代方法。血小板计数的快速改善表明SE可能是一种可行的紧急治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Emergent splenic embolization for refractory immune thrombocytopenia with critical bleeding: a case report.

Emergent splenic embolization for refractory immune thrombocytopenia with critical bleeding: a case report.

Background: Immune thrombocytopenia (ITP) is characterized by decreased platelet count due to immunological mechanisms. First-line treatment is corticosteroids, with thrombopoietin receptor agonists, rituximab, and splenectomy as second-line options. While surgical splenectomy is effective, it poses high bleeding risks in severe thrombocytopenia. Splenic embolization (SE) is considered an alternative to splenectomy for the treatment of steroid-refractory chronic ITP and has been reported to be an effective and minimally invasive option. However, there are few reports of SE being performed for acute ITP with life-threatening bleeding.

Case description: A 63-year-old man presented in shock with oral bleeding, bloody stools, and recurrent syncope. Laboratory tests revealed severe thrombocytopenia (4,000/mm3 platelets) and elevated platelet-associated immunoglobulin G (PA-IgG), leading to ITP diagnosis. Despite platelet transfusions, intravenous immunoglobulin, and high-dose steroids, his condition worsened with alveolar hemorrhage developing on day 3. Given the surgical risks, emergency SE was performed on day 5 using coils and gelatin sponge. Following SE and thrombopoietin receptor agonist administration, platelet counts improved from day 6, allowing discontinuation of transfusions by day 11. The patient was discharged from the intensive care unit on day 12 with stabilized platelets and improved respiratory status.

Conclusions: This case demonstrates that emergency SE can be an effective and safe alternative to splenectomy for refractory ITP with life-threatening bleeding, particularly when severe thrombocytopenia precludes surgical intervention. The rapid improvement in platelet counts suggests SE could be a viable emergency treatment option.

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