Membranous nephropathy and pulmonary alveolar proteinosis

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Abstract

A 47-year-old woman with a severe cough and high-grade fever demonstrated proteinuria of 3.2 g/day. Chest radiograph and CT scan revealed scattered small nodules and ground-glass opacities with interlobular septal thickening in both lungs. The serum levels of surfactant A, surfactant D, gnd KL-6 were increased to 190 ng/ml (normal: 0-43.8), 360 ng/ml (normal:0-110), and 4856 U/ml (normal: 0-500), respectively. Video-assisted thoracoscopic lung biopsy revealed eosinophilic amorphous material within alveoli and thickened alveolar septa, which is compatible with pulmonary alveolar proteinosis. Kidney biopsy exhibited membranous nephropathy (Stage I-II) accompanied by granular IgG deposition along the glomerular basement membrane. Although the patient refused treatment with granulocyte macropbage colony stimulating factor (GM-CSF) for pulmonary alveolar roteinosis, her proteinuria and the pulmonary lesion gradually diminished and disappeared after one year. © 2007 The Japanese Society of Internal Medicine.

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APA

Yamada, H., Miura, N., Kitagawa, W., Kashima, Y., Matsui, S., Ozeki, N., … Imai, H. (2007). Membranous nephropathy and pulmonary alveolar proteinosis. Internal Medicine, 46(17), 1441–1446. https://doi.org/10.2169/internalmedicine.46.0129

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