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本文引用的文献

1
HIV treatment and associated mitochondrial pathology: review of 25 years of in vitro, animal, and human studies.艾滋病病毒治疗与相关线粒体病理学：对25年体外、动物和人体研究的综述
Toxicol Pathol. 2014 Jul;42(5):811-22. doi: 10.1177/0192623313503519. Epub 2013 Sep 25.
2
A risk prediction score for kidney failure or mortality in rhabdomyolysis.横纹肌溶解症致肾衰竭或死亡的风险预测评分。
JAMA Intern Med. 2013 Oct 28;173(19):1821-8. doi: 10.1001/jamainternmed.2013.9774.
3
Renal involvement in mitochondrial cytopathies.线粒体细胞病变相关性肾损伤
Pediatr Nephrol. 2012 Apr;27(4):539-50. doi: 10.1007/s00467-011-1926-6. Epub 2011 Jun 9.
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Searching for the needle in the Haystacks.大海捞针
Lancet. 2009 Sep 5;374(9692):850. doi: 10.1016/S0140-6736(09)61032-1.
5
Multisystem manifestations of mitochondrial disorders.线粒体疾病的多系统表现。
J Neurol. 2009 May;256(5):693-710. doi: 10.1007/s00415-009-5028-3. Epub 2009 Mar 1.
6
Early coenzyme Q10 supplementation in primary coenzyme Q10 deficiency.原发性辅酶Q10缺乏症的早期辅酶Q10补充治疗
N Engl J Med. 2008 Jun 26;358(26):2849-50. doi: 10.1056/NEJMc0800582.
7
COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement.辅酶Q2肾病：一种新描述的以原发性肾脏受累为特征的遗传性线粒体病。
J Am Soc Nephrol. 2007 Oct;18(10):2773-80. doi: 10.1681/ASN.2006080833. Epub 2007 Sep 12.
8
Renal pathology in children with mitochondrial diseases.线粒体疾病患儿的肾脏病理学
Pediatr Nephrol. 2005 Sep;20(9):1299-305. doi: 10.1007/s00467-005-1948-z. Epub 2005 Jun 24.
9
Acute renal failure due to carnitine palmitoyltransferase II deficiency.肉碱棕榈酰转移酶II缺乏所致的急性肾衰竭
Neth J Med. 2003 Dec;61(12):417-20.
10
Mitochondrial DNA depletion and respiratory chain enzyme deficiencies are present in peripheral blood mononuclear cells of HIV-infected patients with HAART-related lipodystrophy.线粒体DNA耗竭和呼吸链酶缺乏存在于接受高效抗逆转录病毒治疗（HAART）相关脂肪代谢障碍的HIV感染患者的外周血单个核细胞中。
Antivir Ther. 2003 Aug;8(4):333-8.

复发性急性肾损伤作为线粒体肌病的首发表现

Recurrent episodic acute kidney injury as presenting manifestation of mitochondrial myopathy.

作者信息

Matthai T P, Zachariah U G, Matthai S M

机构信息

Deptartment of Nephrology, St. Mary's Dialysis Centre, Karipal Hospital, Kottayam, Kerala, India.

Department of Hepatology, Central Electron Microscopy Unit, Christian Medical College, Vellore, Tamil Nadu, India.

出版信息

Indian J Nephrol. 2014 Nov;24(6):387-9. doi: 10.4103/0971-4065.133027.

DOI:10.4103/0971-4065.133027
PMID:25484535
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4244721/
Abstract

Mitochondrial cytopathies (MC) are a rare heterogenous group of disorders with frequent multisystem involvement including uncommon renal manifestations. Acute kidney injury (AKI) as the primary manifestation of MC is extremely rare. Here, we report a case of recurrent episodic AKI in an adult male who was subsequently diagnosed to have mitochondrial disease.

摘要

线粒体细胞病（MC）是一组罕见的异质性疾病，常累及多系统，包括少见的肾脏表现。急性肾损伤（AKI）作为MC的主要表现极为罕见。在此，我们报告一例成年男性复发性发作性AKI病例，该患者随后被诊断为线粒体疾病。