首页> 外文期刊>Transfusion and apheresis science: official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis >A post-partum hemolytic-uremic-like-syndrome in a patient with pre-eclampsia: description of a clinical case.
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A post-partum hemolytic-uremic-like-syndrome in a patient with pre-eclampsia: description of a clinical case.

机译:子痫前期患者的产后溶血性尿毒症样综合征:临床病例描述。

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HEMOLYTIC UREMIC SYNDROME POST-PARTUM: We describe a case of a 37-year-old woman admitted for severe renal failure to our hospital immediately after the delivery by caesarean section of twins. She had anuria, anemia, and moderate thrombocytopenia. A diagnosis of hemolytic-uremic syndrome was made. Plasma exchange was started, substitution was performed with fresh frozen plasma and eight consecutive plasmapheresis sessions were given. She received hydrocortisone and ACE inhibitors. After about fifteen days from the beginning of the illness, signs of active haemolysis disappeared and renal function was partially recovered. A genetic study demonstrated the absence of HF1 and MCP mutations but a polymorphic variant of the HF1 gene (C-257T promoter region). This polymorphism is strongly associated with non-diarrhoea-HUS (D-HUS). Post-partum HUS is quite a rare syndrome and has a poor outcome; however prompt diagnosis and efficacious therapy could save lives without clinical consequences. The excellent outcome of this patient seems to corroborate this concept.
机译:产后溶血性尿毒症综合征:我们描述了一名因双胎剖腹产分娩后立即因严重肾功能衰竭入院的37岁妇女的病例。她患有无尿,贫血和中度血小板减少症。诊断为溶血性尿毒症综合征。开始血浆置换,用新鲜的冷冻血浆进行置换,并连续进行八次血浆置换。她接受了氢化可的松和ACE抑制剂。从发病开始约十五天后,活跃的溶血迹象消失,肾功能部分恢复。一项遗传研究表明,没有HF1和MCP突变,但是HF1基因具有多态性(C-257T启动子区域)。这种多态性与非腹泻性HUS(D-HUS)密切相关。产后HUS是一种罕见的综合症,预后差。但是,及时诊断和有效治疗可以挽救生命,而不会产生临床后果。该患者的出色结果似乎证实了这一观点。

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