[糖皮质激素治疗特发性纤维化纵隔炎1例]。

Go Kato, Koichiro Takahashi, Tomonori Abe, Chiho Kakino, Ayako Matsuo, Naomi Kobayashi, Kazutoshi Komiya, Naoko Sueoka-Aragane, Shinichiro Hayashi
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引用次数: 0

摘要

一名54岁男子因用力呼吸困难和胸部压迫感被送入佐贺大学医院。胸部CT示纵隔隆突及左肺门周围低密度肿块,导致左肺动脉及左主支气管狭窄。手术活检的病理结果显示明显的纤维化组织伴淋巴细胞和浆细胞,我们诊断为特发性纤维化性纵隔炎II期。口服糖皮质激素治疗强的松龙30 mg/d可减轻肿块,改善左肺动脉和左主支气管狭窄。给予低剂量糖皮质激素维持治疗。以往的报道表明,特发性纤维化纵隔炎伴严重组织纤维化难以用糖皮质激素单药治疗控制。在这里,我们报告一个特发性纤维化纵隔炎的病例是有效的治疗糖皮质激素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Effective glucocorticoid treatment in a case of idiopathic fibrosing mediastinitis].

A 54-year-old man was admitted to Saga University hospital with dyspnea on effort and a sensation of pressure in the chest. Chest CT images showed a low-density mass in the mediastinum surrounding the carina and left hilus, causing narrowing of both the left pulmonary artery and left main bronchus. The pathological findings from a surgical biopsy showed markedly fibrotic tissue with lymphocytes and plasmacytes, and we diagnosed idiopathic fibrosing mediastinitis, stage II. Oral glucocorticoid treatment of 30 mg/day prednisolone reduced the mass and improved the narrowing of the left pulmonary artery and left main bronchus. The patient was given low-dosage glucocorticoids as maintenance treatment. Previous reports indicated that idiopathic fibrosing mediastinitis with severe tissue fibrosis is difficult to control with glucocorticoid monotherapy. Here, we report a case of idiopathic fibrosing mediastinitis that was effectively treated with glucocorticoids.

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