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多系统线粒体病伴复发性类固醇反应性嗜酸性粒细胞增多症。

Multi-system mitochondrial disorder with recurrent steroid-responsive eosinophilia.

机构信息

Krankenanstalt Rudolfstiftung, Postfach 20, 1180 Vienna, Austria.

出版信息

Rheumatol Int. 2009 Nov;30(1):135-9. doi: 10.1007/s00296-009-0915-6.

Abstract

Though mitochondrial disorders due to a respiratory chain defect may manifest with haematological abnormalities such as anaemia, neutropenia, or thrombocytopenia, recurrent steroid-responsive eosinophilia has not been reported as a manifestation of a mitochondrial disorder. In a polymorbid 65-year old female recurrent erythema, asthma, chronic bronchitis, gastritis with eosinophilic granuloma, recurrent episodes of hypereosinophilia, and polyarthralgia suggested Churg–Strauss syndrome, which was excluded upon absence of eosinophilic vasculitis on any of the biopsies. However, corticosteroids were effective for hypereosinophilia. In addition to the hypereosinophilic syndrome a mitochondrial disorder with multi-system affection was diagnosed upon the clinical presentation and a muscle biopsy indicative of a mitochondrial disorder. Hypereosinophilia was interpreted as a manifestation of the mitochondrial disorder after exclusion of various differentials. Mitochondrial disease may go along with marked eosinophilia mimicking Churg–Strauss syndrome. Steroids may be useful to resolve episodic eosinophilia but may be ineffective for other features of mitochondrial disorders.

摘要

尽管由于呼吸链缺陷引起的线粒体疾病可能表现为血液学异常,如贫血、中性粒细胞减少或血小板减少,但反复类固醇反应性嗜酸性粒细胞增多症尚未被报道为线粒体疾病的表现。在一位多病的 65 岁女性中,反复出现红斑、哮喘、慢性支气管炎、胃炎伴嗜酸性粒细胞肉芽肿、反复出现嗜酸性粒细胞增多症和多发性关节炎,提示变应性肉芽肿性血管炎,但任何活检均未见嗜酸性粒细胞血管炎,因此排除了该诊断。然而,皮质类固醇对嗜酸性粒细胞增多症有效。除了高嗜酸性粒细胞综合征外,还根据临床表现和提示线粒体疾病的肌肉活检诊断出一种多系统受累的线粒体疾病。排除各种鉴别诊断后,将嗜酸性粒细胞增多症解释为线粒体疾病的表现。线粒体疾病可能伴有明显的嗜酸性粒细胞增多,类似于变应性肉芽肿性血管炎。类固醇可能有助于解决阵发性嗜酸性粒细胞增多症,但对线粒体疾病的其他特征可能无效。

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