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Extreme lactic acidosis type B associated with metformin treatment. 极端乳酸性酸中毒B型与二甲双胍治疗相关。
Pub Date : 2011-12-01 Epub Date: 2011-09-14 DOI: 10.1093/ndtplus/sfr110
Andreas Pikwer, Einar Vernersson, Anders Frid, Gunnar Sterner

The elimination of metformin is exclusively through the kidneys and elevated plasma concentrations can cause lactic acidosis. We report a case of severe lactic acidosis (pH 6.60) occuring with ostensibly normal therapeutic doses of metformin in the setting of acute renal failure. Continuous veno-venous haemodiafiltration decreased plasma metformin concentrations from 266 lmol/L at presentation to 68 lmol/L, 21 h later. The patient improved rapidly.

二甲双胍的清除完全通过肾脏,血浆浓度升高可引起乳酸性酸中毒。我们报告一例严重乳酸酸中毒(pH 6.60)发生与表面正常治疗剂量的二甲双胍在设置急性肾功能衰竭。持续的静脉-静脉血液滤过使血浆二甲双胍浓度从出现时的266 lmol/L降至21 h后的68 lmol/L。病人好转得很快。
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引用次数: 6
Successful management of angiomyolipoma of the left kidney. 左肾血管平滑肌脂肪瘤的成功治疗。
Pub Date : 2011-12-01 Epub Date: 2011-08-24 DOI: 10.1093/ndtplus/sfr101
G H Neild, Yuvaram N V Reddy, Yogesh N V Reddy, Deepika Lunawat, Georgi Abraham
A 57-year-old woman with a creatinine of 0.8 mg/dL and a normal urine analysis, was investigated with technetium-99m renogram and multidetector computerized tomography (MDCT) as a renal donor for her daughter. The glomerular filtration rate (GFR) was 100 mL/min with the left kidney 42 mL/min and right kidney 58 mL/ min. MDCT revealed a large lipomatous tumour on the renal cortex of the left lower pole with exophytic extension into the perirenal space measuring 7.3 3 5.2 cm (Figure 1). The arterial phase revealed dual arterial supply to the left kidney with the tumour being supplied by a branch from the lower renal artery (Figure 2a). The presence of fat [67 Hounsfield unit (HU)] with interposed soft tissue (42 HU), ectatic vessels and an aneurysm that measured 9 mm 3 8.9 mm with no direct arteriovenous shunting favoured the diagnosis of angiomyolipoma. Superselective catheterization of the feeding artery was performed and the neovascular vessels were embolized. Post-embolization MDCT revealed complete obliteration of the abnormal feeding artery and the aneurysmal lumen (Figure 2b). A week later, the GFR was 107 mL/min, left kidney 43 mL/min and right kidney 64 mL/min. Angiomyolipoma is a benign renal neoplasm with variable amounts of fat, vascular and smooth muscle elements. Attenuation of less than 20 HU on computerized tomography is widely accepted to confirm the presence of fat and this finding confirms the diagnosis of angiomyolipoma [1]. A tumour >4 cm with an aneurysm measuring >5 mm has a high risk of rupture [2].
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引用次数: 1
The role of hypoxia-inducible factor-1 alpha in TEMPI syndrome. 缺氧诱导因子-1 α在TEMPI综合征中的作用。
Pub Date : 2011-12-01 DOI: 10.1093/ndtplus/sfr143
Sujoy Khan
Sir, Two recent reports in The New England Journal of Medicine on a newly described syndrome, namely TEMPI syndrome (telangiectasia, erythrocytosis, monoclonal paraprotein, paranephric fluid collections, intrapulmonary shunting) are fascinating [1, 2], considering the number of cases where the radiological finding of perinephric fluid collections are not investigated further [3] or the concomitant laboratory finding of a paraprotein is dismissed as another case of monoclonal gammopathy of undetermined significance (MGUS). Sykes et al. [2] hypothesize that the IgG paraprotein in TEMPI syndrome may be pathogenic due to the resolution of most clinical features after a trial with the proteasome inhibitor, bortezomib. But, as bortezomib also affects the function of hypoxia-inducible factor-1 alpha (Hif-1α) and down-stream transcription of vascular endothelial growth factor (VEGF) [4], inhibition of Hif-1α would also explain the resolution of the symptoms seen in the patient described by Sykes et al. Expression of Hif-1α and Hif-1α messenger RNA has been detected in all human tissues [5]. Intratumoral hypoxia is known to induce Hif-1α expression that increases VEGF and angiogenesis, but growth factors and loss-of-function mutations in von Hippel Lindau gene and p53 also induce Hif-1α expression (and possibly development of telangiectasias and erythrocytosis) [6]. Zhang et al. [7] showed that even under normoxic conditions, the oncogenic c-Myc/Hif-1α pathway modulates multiple myeloma cell production and mediates production and secretion of VEGF. Bortezomib was also shown to decrease both c-Myc and Hif-1α levels. Specific inhibitors of Hif-1α may therefore reverse most of the pathological manifestations of TEMPI syndrome.
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引用次数: 5
Developing an assisted automated peritoneal dialysis (aAPD) service-a single-centre experience. 开发辅助自动腹膜透析(aAPD)服务--单中心经验。
Pub Date : 2011-12-01 DOI: 10.1093/ndtplus/sfr130
Nina Brown, Anand Vardhan

There is an ongoing increase in the number of elderly or frail patients requiring renal replacement therapy. Assisted automated peritoneal dialysis (aAPD) is one treatment option for this patient group and is becoming increasingly recognized as a distinct dialysis modality. In this article, we review the current status of aAPD and its evolution across Europe, describing the differences in service provision. We also report our experience locally of outcomes on our aAPD population over the last 4 years. We found that aAPD is a viable dialysis modality in the frail and elderly with limited lifespan, and complications of peritoneal dialysis are perhaps lower than would be expected in this population. This form of therapy also avoids the disruption to life which results from hospital-based dialysis.

需要接受肾脏替代治疗的老年或体弱患者人数不断增加。辅助自动腹膜透析(aAPD)是这类患者的一种治疗选择,作为一种独特的透析方式正日益得到认可。在这篇文章中,我们回顾了辅助腹膜透析的现状及其在欧洲的发展,描述了服务提供方面的差异。我们还报告了过去 4 年中我们在当地对 aAPD 患者的治疗结果。我们发现,对于体弱多病、寿命有限的老年人来说,腹膜透析是一种可行的透析方式,而且腹膜透析的并发症在这类人群中可能低于预期。这种治疗方式还避免了住院透析对生活造成的干扰。
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引用次数: 0
IgM antibodies towards pre-endothelial cells: strong indication for an association with accelerated rejection. A case report. 针对内皮前细胞的IgM抗体:与加速排斥反应相关的强烈迹象。一份病例报告。
Pub Date : 2011-12-01 DOI: 10.1093/ndtplus/sfr147
Maria L Kafetzi, Aliki G Iniotaki, George C Liapis, Maria N Darema, Ilias I N Doxiadis, John N Boletis

A 27-year-old woman developed a graft loss due to an accelerated humoral rejection after receiving a blood group identical, human leucocyte antigens (HLA) haploidentical living-related kidney, despite the fact that she did not refer any sensitization event before transplantation. The complement-dependent cytotoxicity and flow cytometry crossmatches were negative for T and B cells. Retrospectively, IgM antibodies against donor precursor endothelial Tie-2(+) cells were detected using a commercially available assay and the pre-transplant serum sample. This case illustrates the necessity of detection of other than the classical HLA-directed antibodies prior organ grafting.

一名27岁的女性在接受了血型相同的人类白细胞抗原(HLA)单倍体相同的活体相关肾脏后,由于加速的体液排斥反应而发生了移植物丢失,尽管她在移植前没有提到任何致敏事件。T细胞和B细胞补体依赖性细胞毒性和流式细胞术交叉配型均为阴性。回顾性地,使用市售的检测方法和移植前血清样本检测针对供体前体内皮Tie-2(+)细胞的IgM抗体。本病例说明了在器官移植前检测除经典hla定向抗体外的其他抗体的必要性。
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引用次数: 2
Nutcracker phenomenon presenting as loin pain haematuria syndrome. 胡桃夹子现象表现为腰痛血尿综合征。
Pub Date : 2011-12-01 DOI: 10.1093/ndtplus/sfr152
Holly B Vince, Charles R Tomson, Eric J Loveday, Paul A Lear, John B Eastwood

A 19-year-old female presented with bilateral severe loin pain associated with recurrent macroscopic haematuria. A provisional diagnosis of loin pain haematuria syndrome was made; the severity and frequency of pain led to referral to the pain management service. Alternative diagnoses were considered. Although previous reports of obstruction of the left renal vein have not described pain of this severity, magnetic resonance angiography was performed; it showed obstruction of the left renal vein as it passed between the superior mesenteric artery and aorta, i.e. the nutcracker phenomenon. Both pain and haematuria resolved fully after autotransplantation.

一个19岁的女性提出了双侧严重的腰痛,并伴有复发性肉眼血尿。初步诊断为腰痛血尿综合征;疼痛的严重程度和频率导致转介到疼痛管理服务。考虑了其他诊断。虽然先前的左肾静脉梗阻报告没有描述这种严重程度的疼痛,但磁共振血管造影进行了;左肾静脉经肠系膜上动脉与主动脉之间时梗阻,即胡桃钳现象。自体移植后疼痛和血尿完全消失。
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引用次数: 1
Sepsis and a painful shoulder in a haemodialysis patient. 血液透析患者的败血症和肩部疼痛。
Pub Date : 2011-12-01 Epub Date: 2011-07-25 DOI: 10.1093/ndtplus/sfr088
Roshni Rathore, John Cheesbrough, Monika Pasztor, Alex Woywodt
Soft tissue infections are common in patients with end-stage renal failure, particularly those with concomitant diabetes and peripheral vascular disease. They usually affect the lower extremities and their microbiology is dominated by gram-positive organisms. Empirical antibiotic treatment is usually straightforward, and success or failure is heavily influenced by the degree of underlying vascular disease. We present an unusual case of treatment-resistant and eventually fatal soft tissue infection of the shoulder in a maintenance haemodialysis patient with known chronic lymphocytic leukaemia (CLL). We discuss the case with emphasis on the differential diagnosis of unusual soft tissue infections in a dialysis patient. We review possible causes of treatment failure, unusual organisms and implications for treatment.
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引用次数: 1
Anticoagulation and dialysis access practice in home haemodialysis in the UK. 英国家庭血液透析中的抗凝和透析通路实践。
Pub Date : 2011-12-01 DOI: 10.1093/ndtplus/sfr132
Cormac Breen

Anticoagulation is an important component of haemodialysis treatment in all settings. The therapeutic options available for anticoagulation of home haemodialysis are similar to those for haemodialysis in other settings. However, dialysis sessions with a wide range of treatment durations are undertaken at home, which can require different approaches to anticoagulation. Conference delegates were asked about the types of anticoagulation used in home dialysis and about surveillance strategies for monitoring vascular access, and the results are presented and discussed.

抗凝是所有情况下血液透析治疗的重要组成部分。家庭血液透析的抗凝治疗方案与其他环境下的血液透析相似。但是,家庭透析的治疗时间长短不一,因此需要采取不同的抗凝方法。会议代表就家庭透析中使用的抗凝类型以及监测血管通路的监控策略进行了提问,并对结果进行了介绍和讨论。
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引用次数: 0
Home dialysis-an international perspective. 家庭透析——一个国际视角。
Pub Date : 2011-12-01 DOI: 10.1093/ndtplus/sfr129
Martin Wilkie

Background. There is strong evidence from a range of long-term conditions of improved outcomes where patients are involved in self-management. Against this background, the international trend for home dialysis continues to decline, with centre-based haemodialysis continuing its dominance. Methods. An opinion-based commentary exploring practice patterns and drivers for home dialysis internationally. Data are drawn from a number of sources including the 2010 United States Renal Data System report. Results. Drivers behind the use of home dialysis are complex including factors relating to the patient and their carers, health care team, health care system, geography and cultural factors. There are important examples where local champions or public health initiatives have had a positive impact on the use of home dialysis; however, in many settings significant barriers remain. Better systems for giving patient information, shared decision making and involving patients in their own care may have the potential to act as a driver for change. Conclusion. Centre-based haemodialysis continues to dominate renal replacement therapy internationally with notable exceptions. Such dominance suggests that most patients worldwide do not get much choice when it comes to modality selection.

背景。有强有力的证据表明,在患者参与自我管理的长期条件下,结果会有所改善。在这种背景下,家庭透析的国际趋势继续下降,以中心为基础的血液透析继续占主导地位。方法。一个基于意见的评论探索实践模式和驱动家庭透析国际。数据来自多个来源,包括2010年美国肾脏数据系统报告。结果。使用家庭透析背后的驱动因素是复杂的,包括与患者及其护理人员、卫生保健团队、卫生保健系统、地理和文化因素有关的因素。有一些重要的例子表明,地方倡导者或公共卫生倡议对家庭透析的使用产生了积极影响;然而,在许多情况下,仍然存在重大障碍。提供患者信息、共同决策和让患者参与自身护理的更好的系统可能会成为推动变革的动力。结论。以中心为基础的血液透析继续在国际上主导肾脏替代治疗,有明显的例外。这种优势表明,当涉及到模式选择时,世界上大多数患者没有太多选择。
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引用次数: 13
Minimal-change disease as a paraneoplastic syndrome in a patient with ovarian carcinoma. 卵巢癌伴副肿瘤综合征的微小病变。
Pub Date : 2011-12-01 Epub Date: 2011-09-30 DOI: 10.1093/ndtplus/sfr106
Guido R González-Fontal, Juan G Restrepo, Andrés F Henao-Martínez

Minimal-change disease (MCD) is an exceptional paraneoplastic presentation. We are describing the case of an ovarian paraneoplastic nephrotic syndrome. The kidney biopsy was consistent with MCD. Steroids and immunosuppressive therapy were given with no change in the nephrotic-range proteinuria. A complete resolution of the nephrotic syndrome was soon observed with improvement of her clinical condition after five cycles of chemotherapy with paclitaxel and carboplatin and tumor-debulking surgery. Ovarian carcinoma paraneoplastic nephrotic syndrome secondary to MCD is an extremely rare event, which is important to recognize since it is responsive to the standard chemotherapy.

微小变化病(MCD)是一种特殊的副肿瘤表现。我们正在描述一个卵巢副肿瘤肾病综合征的病例。肾活检结果与MCD相符。给予类固醇和免疫抑制治疗,肾范围蛋白尿无变化。在紫杉醇和卡铂化疗5个周期以及肿瘤减积手术后,她的临床状况得到改善,肾病综合征很快得到完全解决。卵巢癌副肿瘤肾病综合征继发于MCD是一种极其罕见的事件,认识到这一点很重要,因为它对标准化疗有反应。
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引用次数: 2
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