[结核后肺后遗症患者过敏性肺曲霉病的晚期诊断:1例死亡]。

Brenda Guendulain-Velázquez
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引用次数: 0

摘要

简介:过敏性肺曲霉病(ABPA)是对烟曲霉抗原的超敏反应。当它与其他肺部疾病重叠时,诊断可能会延迟。我们提出的病例患者的历史,儿童哮喘和结核后肺部后遗症,治疗多年严重哮喘没有改善。ABPA被确诊,但诊断较晚限制了治疗选择,导致了致命的结果。病例报告:一名61岁女性,有儿童哮喘、高血压、睡眠呼吸暂停、慢性肺心病病史,于2000年以肺结核就诊,经治疗后痊愈,留下支气管扩张、氧依赖等后遗症。患者表现为持续性呼吸困难和频繁发作,重度哮喘治疗无改善。临床旁检查:总IgE 2321 IU/mL,嗜酸性粒细胞908.4。皮肤试验及烟曲霉特异性IgG/IgE阳性。ABPA是根据国际人类和动物真菌学学会(ISHAM)的标准诊断的。病人开始服用伊曲康唑和类固醇。然而,他出现了大量咯血,感染性休克,并于2025年3月去世。结论:变应性支气管肺曲霉病是一种免疫介导的疾病。常见于有哮喘或囊性纤维化病史的患者。在易感个体中,曲霉产生一种夸张的免疫反应。在这个病例中,结核病和支气管扩张的病史延误了诊断,导致治疗延迟和致命的并发症。这种情况强调了在支气管扩张、哮喘和囊性纤维化合并难治性呼吸道症状的患者中需要高度怀疑ABPA的必要性。早期诊断和及时治疗可以改善预后,减少潜在的致命并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Late diagnosis of allergic pulmonary aspergillosis in a patient with post-tuberculosis pulmonary sequelae: a fatal case].

Introduction: Allergic pulmonary aspergillosis (ABPA) is a hypersensitivity reaction to Aspergillus fumigatus antigens. Its diagnosis can be delayed when it overlaps with other pulmonary conditions. We present the case of a patient with a history of childhood asthma and post-tuberculosis pulmonary sequelae, treated for years as severe asthma without improvement. ABPA was confirmed, but the late diagnosis limited therapeutic options, resulting in a fatal outcome.

Case report: A 61-year-old woman with a history of childhood asthma, hypertension, sleep apnea, and chronic cor pulmonale presented with pulmonary tuberculosis in 2000, which resolved after treatment, leaving sequelae such as bronchiectasis and oxygen dependence. She presented with persistent dyspnea and frequent exacerbations, with no improvement with treatment for severe asthma. Paraclinical tests: total IgE 2321 IU/mL, eosinophilia 908.4. Skin tests and specific IgG/IgE for Aspergillus fumigatus were positive. ABPA was diagnosed according to the International Society of Human and Animal Mycology (ISHAM) criteria. The patient was started on itraconazole and steroids. However, he developed massive hemoptysis, septic shock, and died in March 2025.

Conclusion: Allergic bronchopulmonary aspergillosis is an immunologically mediated disease. It occurs in patients with a history of asthma or cystic fibrosis. In susceptible individuals, Aspergillus produces an exaggerated immune response. In this case, the history of tuberculosis and bronchiectasis delayed diagnosis, resulting in delayed management and fatal complications. This scenario underscores the need for a high index of suspicion for ABPA in patients with bronchiectasis, asthma, and cystic fibrosis with refractory respiratory symptoms. Early diagnosis and timely treatment can improve the prognosis and reduce potentially fatal complications.

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