Successful Immunoglobulin Treatment in Severe Cryptogenic Organizing Pneumonia Caused by Dermatomyositis

Dong Hoon Lee, J. H. Yeo, Youngil Kim, Seungjun Gim, J. Sohn, J. Yhi
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引用次数: 1

Abstract

In connective tissue diseases, autoantibodies cause pulmonary interstitial inflammation and fibrosis, and patients require treatment with an immunosuppressive agent such as a steroid. Dermatomyositis is an incurable, uncommon form of connective tissue disease that occasionally causes diffuse pulmonary inflammation leading to acute severe respiratory failure. In such cases, the prognosis is very poor despite treatment with high-dose steroid. In the present case, a 46-year-old man was admitted to our hospital with dyspnea. He was diagnosed with dermatomyositis combined with cryptogenic organizing pneumonia (COP) with respiratory failure and underwent treatment with steroid and an immunosuppressive agent, but the COP was not improved. However, the respiratory failure did improve after treatment with intravenous immunoglobulin, which therefore can be considered a treatment option in cases where steroids and immunosuppressive agents are ineffective.
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免疫球蛋白成功治疗皮肌炎引起的严重隐源性组织性肺炎
在结缔组织疾病中,自身抗体引起肺间质炎症和纤维化,患者需要使用免疫抑制剂如类固醇治疗。皮肌炎是一种无法治愈的、罕见的结缔组织疾病,偶尔会引起弥漫性肺部炎症,导致急性严重呼吸衰竭。在这种情况下,尽管使用大剂量类固醇治疗,预后仍很差。在本病例中,一名46岁的男性因呼吸困难入院。他被诊断为皮肌炎合并隐源性组织性肺炎(COP)并呼吸衰竭,并接受类固醇和免疫抑制剂治疗,但COP没有改善。然而,在静脉注射免疫球蛋白治疗后,呼吸衰竭确实有所改善,因此,在类固醇和免疫抑制剂无效的情况下,静脉注射免疫球蛋白可以被认为是一种治疗选择。
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