Thind Gurcharan Singh
Department of TB and Chest Diseases, Medical College Hospital, Amritsar, India.
Lung India. 2009 Oct;26(4):152-4. doi: 10.4103/0970-2113.56355.
Secondary pulmonary alveolar proteinosis (PAP) is rare but may occur in association with malignancy, certain infections, and exposure to inorganic or organic dust and some toxic fumes. This case report describes the second recorded case of PAP due to exposure to cotton dust. A 24-year-old man developed PAP after working as a spinner for eight years without respiratory protection. He was admitted as an emergency patient with very severe dyspnea for four months and cough for several years. Chest X-ray showed bilateral diffuse alveolar consolidation. He died 16 days later, and a diagnosis of acute pulmonary alveolar proteinosis was made at autopsy. The histopathology demonstrated alveoli and respiratory bronchioles filled with characteristic periodic acid Schiff-positive material, which also revealed birefringent bodies of cotton dust under polarized light. Secondary PAP can be fatal and present with acute respiratory failure. The occupational history and characteristic pathology can alert clinicians to the diagnosis.
继发性肺泡蛋白沉积症(PAP)较为罕见,但可能与恶性肿瘤、某些感染、接触无机或有机粉尘以及一些有毒烟雾有关。本病例报告描述了因接触棉尘导致的第二例有记录的PAP病例。一名24岁男性在未采取呼吸防护措施的情况下担任纺纱工8年后患上了PAP。他因极度严重的呼吸困难持续4个月且咳嗽数年而作为急诊患者入院。胸部X线显示双侧弥漫性肺泡实变。他于16天后死亡,尸检诊断为急性肺泡蛋白沉积症。组织病理学显示肺泡和呼吸性细支气管充满特征性的过碘酸希夫染色阳性物质,在偏振光下还可见棉尘的双折射体。继发性PAP可能致命,并表现为急性呼吸衰竭。职业病史和特征性病理可提醒临床医生做出诊断。