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肾移植6年后发生主动脉夹层和严重肾衰竭。

Aortic Dissection and Severe Renal Failure 6 Years After Kidney Transplantation.

作者信息

Dujardin Amaury, Le Fur Awena, Cantarovich Diego

机构信息

Department of Nephrology, Institute of Transplantation, Urology and Nephrology, Nantes University Hospital, Nantes, France.

Department of Nephrology, La Roche-Sur-Yon Hospital, La Roche-Sur-Yon, France.

出版信息

Transplant Direct. 2017 Aug 9;3(9):e202. doi: 10.1097/TXD.0000000000000723. eCollection 2017 Sep.

Abstract

We report the case of a patient with long-term history of hypertension, presenting with transient neurological disorders and severe graft failure several years after kidney transplantation. Cause of end-stage renal disease was hypertensive nephrosclerosis. Chronic hemodialysis lasted for 1 year. After transplantation and throughout follow-up, serum creatinine ranged from 200 to 230 μmol/L and maintenance immunosuppression included sirolimus and low-dose steroids. Six years after transplantation, the patient presented with right hip pain radiating to the lower back, transient aphasia, confusion, and hemiparesis. Surprisingly, progressive anuria was established requiring dialysis. After numerous nonconclusive investigations including renal histology, a contrast computed tomography scan discovered a Stanford B aortic dissection from the left common carotid artery and left subclavian artery to bilateral internal and external iliac arteries, including the right femoral artery. No surgical treatment was opted and hemodialysis, tight control of blood pressure and oral anticoagulation were established. Immunosuppression was lightened to low-dose steroids alone. After 8 months, chronic dialysis was stopped, and today, 22 months after the diagnosis of aortic dissection, the patient is doing well with a still functioning graft (creatinine, 377 μmol/L; modification of diet in renal disease-glomerular filtration rate, 15 mL/min), and without any other immunosuppression than low-dose steroids.

摘要

我们报告了一例有长期高血压病史的患者,在肾移植数年之后出现短暂性神经功能障碍和严重的移植肾失功。终末期肾病的病因是高血压性肾硬化。慢性血液透析持续了1年。移植后及整个随访期间,血清肌酐范围为200至230μmol/L,维持性免疫抑制包括西罗莫司和小剂量类固醇。移植后6年,患者出现放射至下背部的右髋部疼痛、短暂性失语、意识模糊和偏瘫。令人惊讶的是,逐渐出现无尿,需要进行透析。在包括肾脏组织学检查在内的众多无定论的检查之后,计算机断层扫描血管造影发现了一个从左颈总动脉和左锁骨下动脉至双侧髂内、外动脉,包括右股动脉的斯坦福B型主动脉夹层。未选择手术治疗,而是进行血液透析、严格控制血压和口服抗凝治疗。免疫抑制减至仅使用小剂量类固醇。8个月后,停止了慢性透析,如今,在诊断主动脉夹层22个月后,患者情况良好,移植肾仍在发挥功能(肌酐377μmol/L;肾脏病饮食改良-肾小球滤过率15mL/min),除小剂量类固醇外未使用任何其他免疫抑制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7080/5585418/3d827ff10a48/txd-3-e202-g001.jpg

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