Renduchintala Kavita, Pabbathi Smitha, Nanjappa Sowmya, Ramsakal Asha, Greene John
Internal and Hospital Medicine, Moffitt Cancer Center, Tampa, USA.
Internal Medicine, Moffitt Cancer Center, Tampa, USA.
Cureus. 2020 Dec 14;12(12):e12078. doi: 10.7759/cureus.12078.
Alpha-1 antitrypsin deficiency (AATD) is an autosomal dominant genetic disorder that presents with pulmonary complications and is most commonly manifested by panacinar emphysema and chronic obstructive pulmonary disease. A 49-year-old Caucasian female with a history of AATD and chronic tobacco use was referred to both infectious disease and thoracic surgery clinics with worsening cough and chronic intermittent hemoptysis for the evaluation of possible superimposed infection or malignancy. She had previously been treated with multiple antibiotics and Prolastin-CÒ (alpha-1-proteinase inhibitor). Initial CT of the chest showed known chronic bronchiectasis, severe lower lung emphysema, and right-sided lower lobe pulmonary masses. CT-guided biopsy of one mass showed nonspecific inflammation, negative cultures, and negative cytology. Subsequent follow-up with chest CT scans showed a decreasing size of right-sided pulmonary masses and new left-sided nodule formation, which later stabilized in growth. Based on symptoms and radiological and pathological findings, a diagnosis of organizing pneumonia was made. We present an unusual case of bilateral pulmonary masses mimicking infection and malignancy later found to be most consistent with an organizing pneumonia in a patient with underlying AATD.
α-1抗胰蛋白酶缺乏症(AATD)是一种常染色体显性遗传疾病,表现为肺部并发症,最常见的表现是全腺泡型肺气肿和慢性阻塞性肺疾病。一名49岁有AATD病史且长期吸烟的白人女性,因咳嗽加重和慢性间歇性咯血被转诊至传染病科和胸外科门诊,以评估是否可能合并感染或恶性肿瘤。她此前曾接受多种抗生素和普洛拉丝汀-C(α-1蛋白酶抑制剂)治疗。最初的胸部CT显示已知的慢性支气管扩张、严重的下肺肺气肿和右侧下叶肺部肿块。对其中一个肿块进行CT引导下活检,结果显示为非特异性炎症,培养阴性,细胞学检查阴性。随后的胸部CT随访显示右侧肺部肿块缩小,左侧出现新的结节形成,随后结节生长稳定。根据症状以及影像学和病理学检查结果,诊断为机化性肺炎。我们报告了一例不寻常的病例,该患者双侧肺部肿块最初疑似感染和恶性肿瘤,后来发现最符合潜在AATD患者的机化性肺炎表现。