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Nephrogenic systemic fibrosis: risk factors suggested from Japanese published cases

机译:肾源性系统性纤维化:日本公布病例提示的危险因素

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摘要

The aim of this article is to review the published cases of nephrogenic systemic fibrosis (NSF) in Japan. The Japanese medical literature database and MedLine were searched using the keywords NSF and nephrogenic fibrosing dermopathy (January 2000 to March 2009). Reports in peer-reviewed journals and meeting abstracts were included, and cases with biopsy confirmation were selected. 14 biopsy-verified NSF cases were found. In seven of eight patients reported after the association between gadolinium-based contrast agent (GBCA) and NSF was proposed, GBCA administration was documented: five received only gadodiamide; two received both gadodiamide and gadopentetate dimeglumine. In four cases, the amounts of contrast agent were registered: two received only a single dose (0.1 mmol kg−1 body weight) whereas the other two received 7–15 ml (the body weight was not disclosed) for each MR examination. Five patients had multiple injections of GBCA before NSF developed. Except for one patient in whom renal assessment was not reported, none of the patients had an estimated glomerular filtration rate >30 ml min−1 1.73 m−2 and all received dialysis. 5 of the 8 patients (63%) in whom GBCA exposure was confirmed were treated with peritoneal dialysis. Skin lesion of the lower extremity was the first symptom in 12 patients (86%), whereas 2 patients had primarily symptoms from the upper extremity. In three cases, GBCA was administered even after onset of the NSF symptoms because of the physicians' lack of knowledge about the possible association between GBCA and NSF. NSF is found among Japanese end-stage renal failure patients even after examinations using a single dose.
机译:本文的目的是回顾日本已发表的肾源性系统性纤维化(NSF)病例。使用关键字NSF和肾原性纤维化皮肤病(2000年1月至2009年3月)搜索了日本医学文献数据库和MedLine。包括同行评审期刊和会议摘要中的报告,并选择经活检确认的病例。发现14例经活检证实的NSF病例。在提议将g基造影剂(GBCA)与NSF联用后报道的八例患者中,有七例记录了GBCA的给药:五例仅接受了gadodiamide;三例仅接受了gadodiamide。两人同时接受了加多巴胺和加多戊酸酯二甲双胍。在四种情况下,记录了造影剂的量:两个仅接受单剂量(0.1 mmol kg -1 体重),而另外两个仅接受7–15 ml(未披露体重) )进行每次MR检查。 NSF发生前,五名患者多次注射GBCA。除未报告肾脏评估的一名患者外,所有患者的肾小球滤过率估计均不超过30 ml min -1 1.73 m -2 ,并且均接受了透析。确诊为GBCA的8例患者中有5例(63%)接受了腹膜透析治疗。下肢皮肤病变是12例患者的首发症状(86%),而2例患者主要是上肢症状。在三例病例中,由于医师对GBCA和NSF之间可能的关联性缺乏了解,因此即使在NSF症状发作后仍要给予GBCA。即使在使用单剂量检查后,在日本终末期肾衰竭患者中也发现了NSF。

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