Abstract
Pulmonary sclerosing pneumocytoma (PSP) is a rare benign neoplasm that predominantly affects middle-aged Asian women. PSP is often asymptomatic and demonstrates a solitary pulmonary nodule on radiologic examination. We report a case of PSP initially misdiagnosed as lung cancer because of strong 18F-fluorodeoxyglucose (FDG) uptake revealed by 18F-FDG positron emission tomography-computed tomography scan. After surgery, pathology revealed that the tumor cells were immunopositive for epithelial membrane antigen and thyroid transcription factor-1. The patient has been followed up without complication or recurrence.
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Lim, J. H., Lee, N., Choi, D. W., Oh, H. J., Park, H. Y., Kim, K. H., … Oh, I. J. (2016). Pulmonary sclerosing pneumocytoma mimicking lung cancer: Case report and review of the literature. Thoracic Cancer, 7(4), 508–511. https://doi.org/10.1111/1759-7714.12341
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