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

被引:5
|
作者
Turudic, Daniel [1 ]
Milosevic, Danko [2 ,3 ,4 ]
Bilic, Katarina [2 ,5 ,6 ]
Prohaszka, Zoltan
Bilic, Ernest [1 ,2 ]
机构
[1] Univ Hosp Ctr Zagreb, Dept Pediat Hematol & Oncol, Kispaticeva 12, Zagreb 10000, Croatia
[2] Univ Zagreb, Sch Med, Salata 3, Zagreb 10000, Croatia
[3] Gen Hosp Zabok, Dept Pediat, Bracak 8, Bracak 49210, Croatia
[4] Hosp Croatian Vet, Bracak 8, Bracak 49210, Croatia
[5] Semmelweis Univ, Dept Internal Med & Haematol, H-1085 Budapest, Hungary
[6] Semmelweis Univ, Res Grp Immunol & Haematol, H-1085 Budapest, Hungary
关键词
atypical hemolytic uremic syndrome; acute lymphoblastic leukemia; 6-mercaptopurine; drug-induced; child; PLATELET RATIO INDEX; THROMBOTIC THROMBOCYTOPENIC PURPURA; ASPARTATE-AMINOTRANSFERASE; LIVER FIBROSIS; CIRRHOSIS; APRI; FORM;
D O I
10.3390/jcm11102779
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 Potential undiagnosed/unpublished cases may be assumed.
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页数:10
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