Godoy I, Leite R M, Yoo H H, Defaveri J, Catâneo A J, Queluz T H
Department of Internal Medicine, Botucatu School of Medicine, Universidade Estadual Paulista, Brazil.
Am J Med Sci. 2000 Jun;319(6):411-3. doi: 10.1097/00000441-200006000-00012.
This report describes a case of a 49-year-old man with cough, recurrent hemoptysis, and dyspnea during 18 months, presenting with radiological findings of alveolar infiltrate and cystic lesions in left upper lobe. Laboratory studies revealed normocytic hypochromic anemia and normal coagulation tests. C-reactive protein and mucoproteins were negative. Serum protein electrophoresis and complement, urinalysis, serum creatinine, creatinine clearance, and 24-hour urine protein were normal. Tests for antineutrophil cytoplasmic antibodies and anti-glomerular-basement membrane antibodies were negative. Tests for connective tissue diseases were all negative. Histological findings were consistent with those of idiopathic pulmonary hemosiderosis. Radiological findings are discussed.
本报告描述了一名49岁男性病例,该患者在18个月内出现咳嗽、反复咯血和呼吸困难,胸部影像学检查显示左上叶有肺泡浸润和囊性病变。实验室检查显示正细胞低色素性贫血,凝血功能检查正常。C反应蛋白和粘蛋白为阴性。血清蛋白电泳、补体、尿液分析、血清肌酐、肌酐清除率和24小时尿蛋白均正常。抗中性粒细胞胞浆抗体和抗肾小球基底膜抗体检测为阴性。结缔组织病相关检查均为阴性。组织学检查结果与特发性肺含铁血黄素沉着症相符。文中对影像学检查结果进行了讨论。