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[复发性非典型溶血尿毒综合征的成功预防性血浆输注]

[Successful prophylactic plasma infusions in recurrent atypical hemolytic-uremic syndrome].

作者信息

Zurowska Aleksandra, Załuska-Leśniewska Iga, Hladny-Czerska Wanda

机构信息

Klinika Nefrologii Dzieciecej, Akademii Medycznej w Gdańsku.

出版信息

Przegl Lek. 2006;63 Suppl 3:223-5.

Abstract

UNLABELLED

Atypical, recurrent hemolytic uraemic syndrome (HUS) often leads to end-stage renal disease and can relapse after a renal transplantation. Plasmapheresis and fresh frozen plasma (FFP) therapies are used to treat acute relapses. We report on the prophylactic use of FFP in a child with atypical recurrent HUS with low serum C3. The girl experienced four episodes of atypical HUS over a year from the age of 18 months. During the first relapse a decreased level of C3--0,62 g/l (normal: 0.88-2.01 g/l) was revealed. Initially daily plasma infusions were given (8-14 ml/kg for 5-15 days) during acute episodes. Following the 4th episode prophylactic FFP therapy was started. Three-times weekly plasma transfusions were continued for three months and then doses were tapered off over the next months to once-weekly FFP. During the one year follow-up no relapse has been observed. At the age of 3 1/2 years she is thriving (10th percentile for height and weight). She has severe but well controlled hypertension without end-organ involvement. The child demonstrates signs of stage 2 chronic kidney disease (CKD): serum creatinine--0.65 mg/dl, Schwartz estimated GFR--79.9 ml/min/ 1.73 m2, persistent slight proteinuria and haematuria, increased renal cortical echogenicity on ultrasound. Genetic studies for the known atypical HUS mutations and assessment of complement activation proteins (factors H and I) are under investigation.

CONCLUSION

Prophylactic FFP infusions can be successful in preventing relapses and further progressive renal damage in individual patients with atypical HUS associated with low C3.

摘要

未标注

非典型复发性溶血尿毒综合征(HUS)常导致终末期肾病,且肾移植后可能复发。血浆置换和新鲜冰冻血浆(FFP)疗法用于治疗急性复发。我们报告了对一名血清C3水平低的非典型复发性HUS患儿预防性使用FFP的情况。该女孩从18个月大起的一年中经历了4次非典型HUS发作。在首次复发时,发现C3水平降低至0.62g/L(正常范围:0.88 - 2.01g/L)。急性发作期间最初每日输注血浆(8 - 14ml/kg,持续5 - 15天)。第4次发作后开始预防性FFP治疗。每周3次血浆输注持续3个月,然后在接下来的几个月中逐渐减少剂量至每周1次FFP。在1年的随访中未观察到复发。3岁半时,她生长发育良好(身高和体重处于第10百分位)。她患有严重但控制良好的高血压,无终末器官受累。该患儿表现出2期慢性肾脏病(CKD)的体征:血清肌酐 - 0.65mg/dl,施瓦茨估算的肾小球滤过率 - 79.9ml/min/1.73m²,持续轻度蛋白尿和血尿,超声显示肾皮质回声增强。针对已知非典型HUS突变的基因研究以及补体激活蛋白(因子H和I)的评估正在进行中。

结论

预防性输注FFP对于预防非典型HUS且C3水平低的个体患者复发及进一步的进行性肾损害可能是成功的。

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