Acute Renal Thrombotic Microangiopathy Caused by Eltrombopag and Romiplostim in a Patient with Myelodysplastic Syndromes (MDS) and Underlying Antiphospholipid Syndrome.

Q3 Medicine
European journal of case reports in internal medicine Pub Date : 2024-05-31 eCollection Date: 2024-01-01 DOI:10.12890/2024_004564
Nikhil Sood, Margarita Kushnir, Bindu Jayavelu
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Abstract

Romiplostim and eltrombopag are synthetic agonists of the thrombopoietin receptor (TPO-R), commonly used for immune thrombocytopenic purpura (ITP) and sometimes in myelodysplastic syndrome (MDS). They are rarely associated with kidney injury. We report a case of acute kidney injury caused by romiplostim and eltrombopag in an 80-year-old male patient with MDS and ITP. He did not have systemic haemolysis syndrome but isolated acute renal thrombotic microangiopathy confirmed by kidney biopsy. He was treated with steroids, plasmapheresis and anticoagulation, with improvement in renal function. Interestingly, the patient had high antiphospholipid (aPL) antibodies noted upon screening, indicating a possible new antiphospholipid syndrome (APS) diagnosis. In the presence of circulating aPL antibodies, eltrombopag may have served as a trigger, causing endothelial injury and subsequent renal microangiopathy; aPL antibodies were still significantly positive at four weeks of outpatient testing. This case and a few others reported in the literature highlight the importance of screening for aPL antibodies before initiating TPO-R agonists in patients with ITP. We suspect that using TPO-R agonists, rather than underlying aPL, caused renal failure.

Learning points: Synthetic agonists of the thrombopoietin receptor, such as romiplostim or eltrombopag, can cause acute renal failure.Preexisting antiphospholipid (aPL) antibodies may increase the risk of renal failure.Screening for aPL antibodies should be considered before initiating thrombopoietin-receptor agonists (TPO-R agonists) in patients with immune thrombocytopenic purpura (ITP).

骨髓增生异常综合征 (MDS) 和潜在抗磷脂综合征患者因使用 Eltrombopag 和 Romiplostim 而引发的急性肾血栓性微血管病。
Romiplostim 和 eltrombopag 是血小板生成素受体(TPO-R)的合成激动剂,常用于治疗免疫性血小板减少性紫癜(ITP),有时也用于骨髓增生异常综合征(MDS)。这些药物很少与肾损伤有关。我们报告了一例由罗米波司汀和艾曲波帕引起的急性肾损伤病例,患者是一名 80 岁的男性 MDS 和 ITP 患者。他没有全身溶血综合征,但经肾活检证实患有孤立的急性肾血栓性微血管病。他接受了类固醇、血浆置换和抗凝治疗,肾功能有所改善。有趣的是,患者在筛查时发现了高抗磷脂(aPL)抗体,这表明他可能被诊断为新的抗磷脂综合征(APS)。在循环中存在 aPL 抗体的情况下,艾曲波帕可能成为诱因,导致内皮损伤和随后的肾脏微血管病变;在四周的门诊检测中,aPL 抗体仍呈显著阳性。该病例和文献中报道的其他一些病例强调了在对 ITP 患者使用 TPO-R 激动剂前筛查 aPL 抗体的重要性。我们怀疑是使用 TPO-R 激动剂而非潜在的 aPL 导致了肾衰竭:免疫性血小板减少性紫癜(ITP)患者在使用促血小板生成素受体激动剂(TPO-R激动剂)前应考虑筛查aPL抗体。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
166
审稿时长
8 weeks
期刊介绍: The European Journal of Case Reports in Internal Medicine is an official journal of the European Federation of Internal Medicine (EFIM), representing 35 national societies from 33 European countries. The Journal''s mission is to promote the best medical practice and innovation in the field of acute and general medicine. It also provides a forum for internal medicine doctors where they can share new approaches with the aim of improving diagnostic and clinical skills in this field. EJCRIM welcomes high-quality case reports describing unusual or complex cases that an internist may encounter in everyday practice. The cases should either demonstrate the appropriateness of a diagnostic/therapeutic approach, describe a new procedure or maneuver, or show unusual manifestations of a disease or unexpected reactions. The Journal only accepts and publishes those case reports whose learning points provide new insight and/or contribute to advancing medical knowledge both in terms of diagnostics and therapeutic approaches. Case reports of medical errors, therefore, are also welcome as long as they provide innovative measures on how to prevent them in the current practice (Instructive Errors). The Journal may also consider brief and reasoned reports on issues relevant to the practice of Internal Medicine, as well as Abstracts submitted to the scientific meetings of acknowledged medical societies.
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