Department of Chest Diseases, Atatürk Chest Diseases and Thoracic Surgery Training and Research Hospital, Ankara, Turkey.
Ann Thorac Med. 2011 Oct;6(4):237-40. doi: 10.4103/1817-1737.84781.
Pulmonary alveolar microlithiasis (PAM) is an uncommon lung disease characterized by accumulation of intraalveolar calcifications. The disease can be diagnosed based on the radiological findings. We present a 27-year-old women with five-year history of shortness of breath. She was diagnosed with PAM due to the presence of the characteristic chest X-ray and thorax computed tomography (CT) findings. We performed (18)F-fluorodeoxyglucose (FDG)-PET/CT imaging in order to detect any evidence of inflamation in the lung before deciding an anti-inflammatory treatment. The lung regions with dense calcifications revealed low FDG uptakes (SUVmax: 2.7) and the lung regions without calcifications showed lower FDG uptakes. No further treatment modality was planned besides inhaler salbutamol. Herein, we discuss this rare entity with literature search.
肺肺泡微结石症(PAM)是一种罕见的肺部疾病,其特征为肺泡内钙沉积。该疾病可基于影像学发现进行诊断。我们报告了一例 27 岁女性,其病史为五年呼吸困难。由于存在特征性的胸部 X 线和胸部 CT(CT)表现,她被诊断为 PAM。我们进行了(18)F-氟脱氧葡萄糖(FDG)-PET/CT 成像,以便在决定进行抗炎治疗之前检测肺部是否有炎症的证据。致密钙化的肺区域显示出低 FDG 摄取(SUVmax:2.7),而无钙化的肺区域显示出较低的 FDG 摄取。除了吸入沙丁胺醇外,没有计划进行其他治疗方式。在此,我们通过文献检索讨论了这种罕见的实体。