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1例由裂褶菌引起的变应性支气管肺真菌病伴高密度黏液嵌塞

[A case of allergic bronchopulmonary mycosis caused by Schizophyllum commune presenting with hyperattenuated mucoid impaction].

作者信息

Uruga Hironori, Imafuku Aya, Hanada Shigeo, Takaya Hisashi, Miyamoto Atsushi, Sugimoto Hideyasu, Morokawa Nasa, Kurosaki Atsuko, Fujii Takeshi, Kishi Kazuma

机构信息

Department of Respiratory Medicine, Respiratory Center, Toranomon Hospital.

出版信息

Nihon Kokyuki Gakkai Zasshi. 2010 Oct;48(10):749-54.

Abstract

A 64-year-old woman was admitted to our hospital because of cough, bloody sputum and chest pain in January 2007. Chest computed tomography (CT) on admission revealed hyperattenuated mucoid impaction and consolidation in the right S3b. She was given a diagnosis of allergic bronchopulmonary mycosis caused by Schizophyllum commune. Treatment with 200 mg/day itraconazole and 15 mg/day oral prednisolone was begun, and her symptoms and consolidation resolved. In December 2007, consolidation in the left lower lobe appeared after itraconazole was stopped and replaced with oral prednisolone with inhaled fluticasone propionate. She again received 200 mg/day itraconazole and 15 mg/day oral prednisolone, resulting in a reduction in her consolidation. In May 2008, itraconazole was stopped and oral prednisolone was changed to inhaled salmeterol fluticasone propionate. In November 2008, her symptoms appeared again, and chest CT demonstrated hyperattenuated mucoid impaction and consolidation in the right S8. A transbronchial biopsy revealed granulomatosis, Charcot-Leyden crystals, and mucus infiltrated by eosinophils and fungi. Schizophyllum commune was isolated from her bronchial lavage fluid. A recurrence of allergic bronchopulmonary mycosis was diagnosed. Retreatment with itraconazole and oral prednisolone resulted in improvement of her symptoms and chest radiographic findings. To the best of our knowledge this is the first reported case of allergic bronchopulmonary mycosis caused by Schizophyllum commune presenting with hyperattenuated mucoid impaction.

摘要

2007年1月,一名64岁女性因咳嗽、咯血和胸痛入住我院。入院时胸部计算机断层扫描(CT)显示右肺上叶S3b段有高密度黏液嵌塞和实变。她被诊断为裂褶菌引起的过敏性支气管肺真菌病。开始使用伊曲康唑200mg/天和口服泼尼松龙15mg/天进行治疗,她的症状和实变情况得到缓解。2007年12月,停用伊曲康唑并换用口服泼尼松龙加吸入丙酸氟替卡松后,左下叶出现实变。她再次接受伊曲康唑200mg/天和口服泼尼松龙15mg/天治疗,实变情况有所减轻。2008年5月,停用伊曲康唑,将口服泼尼松龙改为吸入沙美特罗替卡松丙酸酯。2008年11月,她的症状再次出现,胸部CT显示右肺下叶S8段有高密度黏液嵌塞和实变。经支气管活检显示肉芽肿、夏科-莱登结晶,以及嗜酸性粒细胞和真菌浸润的黏液。从她的支气管灌洗液中分离出裂褶菌。诊断为过敏性支气管肺真菌病复发。再次使用伊曲康唑和口服泼尼松龙治疗后,她的症状和胸部影像学表现有所改善。据我们所知,这是首例由裂褶菌引起的过敏性支气管肺真菌病伴高密度黏液嵌塞的报道病例。

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