Akpa Bimaje, Desai Hem
Department of Pulmonary, Allergy, Critical Care and Sleep Medicine, University of Minnesota Medical School, USA.
Respir Med Case Rep. 2024 Feb 13;48:101994. doi: 10.1016/j.rmcr.2024.101994. eCollection 2024.
Unilateral absence of pulmonary artery (UAPA) is a congenital clinical abnormality that is rarely diagnosed in adulthood. Due to its rarity and heterogeneity as it pertains to its clinical presentation, it may be difficult to diagnose, often leading to misdiagnosis. We present a case of UAPA with unilateral pulmonary fibrosis which was misdiagnosed as rheumatoid arthritis-associated interstitial lung disease (RA-ILD). We describe the symptomology, physical examination findings, laboratory values and radiologic findings. We also describe the diagnostic challenges and approach to a patient presenting with unilateral interstitial lung disease (ILD) and highlight the importance of a comprehensive evaluation.
单侧肺动脉缺如(UAPA)是一种先天性临床异常,在成年期很少被诊断出来。由于其罕见性以及临床表现的异质性,可能难以诊断,常常导致误诊。我们报告一例伴有单侧肺纤维化的UAPA病例,该病例最初被误诊为类风湿关节炎相关间质性肺病(RA-ILD)。我们描述了症状、体格检查结果、实验室检查值和影像学检查结果。我们还描述了诊断面临的挑战以及对单侧间质性肺病(ILD)患者的诊断方法,并强调了综合评估的重要性。