Department of Internal Medicine, Morehouse School of Medicine, Atlanta, GA, USA.
Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, USA.
Am J Case Rep. 2020 Dec 28;21:e928499. doi: 10.12659/AJCR.928499.
BACKGROUND Invasive pulmonary aspergillosis (IPA) is a severe form of the fungal infection with relatively high mortality rates. Risk factors that lead to IPA include immunosuppression through corticosteroid use. IPA complicated by hydropneumothorax is rare and its mechanism of formation is unknown. CASE REPORT A 72-year-old woman recently diagnosed with a right frontal meningioma that was managed with dexamethasone presented with a new 3-day history of nonproductive cough, chest pain, and dyspnea and was managed for pneumonia. The patient failed to improve, prompting a follow-up computed tomography scan, which revealed a right middle lobe cavitary lesion. During the workup of this lesion, the patient's hospital course was complicated by hemoptysis and development of a large right hydropneumothorax that was successfully managed with a chest tube. Despite initial resolution of hydropneumothorax, the patient developed a right apical pneumothorax that gradually worsened. Bronchoscopy culture revealed Aspergillus fumigatus, leading to the diagnosis of IPA, which was managed with intravenous voriconazole. CONCLUSIONS Corticosteroid use with subsequent immunosuppression is a risk factor for developing IPA. Clinicians should include IPA in their differential diagnosis for respiratory infections in patients receiving corticosteroids. Although overall prognosis of IPA is poor, outcomes can be improved with early diagnosis, early empiric initiation of antifungals, and withdrawal of immunosuppressive therapy. IPA complicated by hydropneumothorax is a rare phenomenon with a poorly understood mechanism of formation. Based on our case, we propose a mechanism of hydropneumothorax formation from IPA.
侵袭性肺曲霉病(IPA)是一种严重的真菌感染形式,死亡率相对较高。导致 IPA 的危险因素包括使用皮质类固醇的免疫抑制。IPA 并发液气胸较为罕见,其形成机制尚不清楚。
一名 72 岁女性,最近被诊断出患有右侧额部脑膜瘤,采用地塞米松治疗,出现了新的 3 天无痰咳嗽、胸痛和呼吸困难,被诊断为肺炎。患者病情未见改善,促使进行了后续的计算机断层扫描,显示右侧中叶空洞性病变。在对该病变进行检查的过程中,患者的住院过程出现了咯血,并发生了大量右侧液气胸,经胸腔引流管成功治疗。尽管最初的液气胸得到了缓解,但患者出现了右侧尖顶气胸,逐渐加重。支气管镜培养显示烟曲霉,导致 IPA 的诊断,采用静脉伏立康唑治疗。
皮质类固醇的使用及随后的免疫抑制是发生 IPA 的危险因素。临床医生应将 IPA 纳入接受皮质类固醇治疗的患者发生呼吸道感染的鉴别诊断中。虽然 IPA 的总体预后较差,但早期诊断、早期经验性抗真菌治疗和免疫抑制治疗的停药可以改善预后。IPA 并发液气胸较为罕见,其形成机制尚不清楚。基于我们的病例,我们提出了 IPA 引起液气胸形成的机制。