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一名接受维持治疗的非典型溶血性尿毒症综合征合并前体B细胞急性淋巴细胞白血病儿童使用依库珠单抗的有限疗程:病例报告及文献综述

A Limited Course of Eculizumab in a Child with the Atypical Hemolytic Uremic Syndrome and Pre-B Acute Lymphoblastic Leukemia on Maintenance Therapy: Case Report and Literature Review.

作者信息

Turudic Daniel, Milosevic Danko, Bilic Katarina, Prohászka Zoltán, Bilic Ernest

机构信息

Department of Pediatric Hematology and Oncology, University Hospital Centre Zagreb, Kispaticeva 12, 10000 Zagreb, Croatia.

School of Medicine, University of Zagreb, Šalata 3, 10000 Zagreb, Croatia.

出版信息

J Clin Med. 2022 May 14;11(10):2779. doi: 10.3390/jcm11102779.

Abstract

Acute lymphoblastic leukemia (ALL) is considered a possible risk for the occurrence of thrombotic microangiopathies. We present a girl with pre-B ALL successfully treated according to the BFM ALL IC-2009 protocol on maintenance therapy followed by aHUS occurrence. This is the seventh case of HUS/aHUS on ALL maintenance therapy and the first with clearly documented eculizumab use in the early stage of aHUS/secondary TMA. Standard and additional parameters were used in aHUS monitoring alongside the reticulocyte production index adjusted for age (RPI/A) and the aspartate aminotransferase-to-platelet ratio index (APRI) as markers of hemolysis and rapid response following treatment. RPI/A and APRI are markers of bone marrow response to anemia serving as red blood cell vs. platelet recovery markers. Together they mark the exact recovery point of thrombotic microangiopathy and serve as a prognostic marker of eculizumab treatment success. During the 8-month treatment and 6-month follow-up, no recurrence of hemolysis, ALL relapse, or renal damage were observed. A systematic review of the literature revealed 14/312 articles; five children had aHUS before the onset of ALL, and two children had both diseases concurrently. At least 3/7 patients are attributed to aHUS, of whom 2/7 have renal damage. Potential undiagnosed/unpublished cases may be assumed.

摘要

急性淋巴细胞白血病(ALL)被认为是发生血栓性微血管病的一个潜在风险因素。我们报告了一名前B细胞ALL女童,按照BFM ALL IC - 2009方案成功接受维持治疗后发生了非典型溶血尿毒综合征(aHUS)。这是ALL维持治疗期间发生HUS/aHUS的第7例病例,也是首例在aHUS/继发性血栓性微血管病(TMA)早期明确记录使用依库珠单抗治疗的病例。在aHUS监测中,除了使用标准参数和其他参数外,还采用了根据年龄调整的网织红细胞生成指数(RPI/A)和天冬氨酸转氨酶与血小板比值指数(APRI)作为溶血及治疗后快速反应的标志物。RPI/A和APRI是骨髓对贫血反应的标志物,可作为红细胞与血小板恢复的标志物。它们共同标志着血栓性微血管病的确切恢复点,并作为依库珠单抗治疗成功的预后标志物。在8个月的治疗期和6个月的随访期内,未观察到溶血复发、ALL复发或肾损害。对文献进行系统回顾后发现了14/312篇文章;5名儿童在ALL发病前就患有aHUS,2名儿童同时患有这两种疾病。至少3/7的患者归因于aHUS,其中2/7有肾损害。可能存在未诊断/未发表的病例。

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