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联合复合体I和IV缺乏时呼吸肌的病变

Affection of the Respiratory Muscles in Combined Complex I and IV Deficiency.

作者信息

Finsterer Josef, Rauschka Helmut, Segal Liane, Kovacs Gabor G, Rolinski Boris

机构信息

Krankenanstalt Rudolfstiftung, Vienna, Austria.

Neurological Department, SMZO-Donauspital, Vienna, Austria.

出版信息

Open Neurol J. 2017 Jan 26;11:1-6. doi: 10.2174/1874205X01711010001. eCollection 2017.

DOI:10.2174/1874205X01711010001
PMID:28217183
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5301300/
Abstract

OBJECTIVES

Combined complex I+IV deficiency has rarely been reported to manifest with the involvement of the respiratory muscles.

CASE REPORT

A 45y male was admitted for hypercapnia due to muscular respiratory insufficiency. He required intubation and mechanical ventilation. He had a previous history of ophthalmoparesis since age 6y, ptosis since age 23y, and anterocollis since at least age 40y. Muscle biopsy from the right deltoid muscle at age 41y was indicative of mitochondrial myopathy. Biochemical investigations revealed a combined complex I+IV defect. Respiratory insufficiency was attributed to mitochondrial myopathy affecting not only the extra-ocular and the axial muscles but also the shoulder girdle and respiratory muscles. In addition to myopathy, he had mitochondrial neuropathy, abnormal EEG, and elevated CSF-protein. Possibly, this is why a single cycle of immunoglobulins was somehow beneficial. For muscular respiratory insufficiency he required tracheostomy and was scheduled for long-term intermittent positive pressure ventilation.

CONCLUSION

Mitochondrial myopathy due to a combined complex I+IV defect with predominant affection of the extra-ocular muscles may progress to involvement of the limb-girdle, axial and respiratory muscles resulting in muscular respiratory insufficiency. In patients with mitochondrial myopathy, neuropathy and elevated cerebrospinal fluid protein, immunoglobulins may be beneficial even for respiratory functions.

摘要

目的

联合性复合体I + IV缺乏症很少有累及呼吸肌的报道。

病例报告

一名45岁男性因肌肉性呼吸功能不全导致高碳酸血症入院。他需要插管和机械通气。他自6岁起有眼肌麻痹病史,自23岁起有上睑下垂病史,至少自40岁起有颈前屈病史。41岁时右侧三角肌肌肉活检提示线粒体肌病。生化检查显示联合性复合体I + IV缺陷。呼吸功能不全归因于线粒体肌病,不仅影响眼外肌和轴性肌肉,还影响肩胛带和呼吸肌。除了肌病外,他还有线粒体神经病变、脑电图异常和脑脊液蛋白升高。可能这就是单次免疫球蛋白治疗有一定益处的原因。因肌肉性呼吸功能不全,他需要进行气管切开术,并计划进行长期间歇性正压通气。

结论

由联合性复合体I + IV缺陷导致的线粒体肌病,以眼外肌受累为主,可能会进展至累及肢带肌、轴性肌肉和呼吸肌,导致肌肉性呼吸功能不全。对于患有线粒体肌病、神经病变和脑脊液蛋白升高的患者,免疫球蛋白甚至对呼吸功能可能有益。