Abstract
Pulmonary sclerosing pneumocytoma (PSP) arising from the hilar lesion is extremely rare. We report an asymptomatic 70-year-old female with a thoracic tumor of unknown origin. Contrast-enhanced chest tomography showed a poorly and heterogeneously enhanced 40-mm tumor compressing the left upper lobe, bronchus, and pulmonary arteries. Positron-emission tomography did not detect abnormal integration in the tumor. Surgical resection was planned to confirm diagnosis and avoid further compression on the structures. Intraoperative findings revealed a dark red-colored tumor, projecting from the left upper lobe in the hilar lesion. Left upper lobectomy was performed through video-assisted thoracoscopic surgery to achieve complete resection and avoid contact bleeding. Immunohistochemical examination revealed the presence of PSP.
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We declare that all authors have no commercial associations that might pose a conflict of interest in connection with the submitted article, especially regarding any materials referred to in this report. No funding for this study was received from any sponsors.
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Ikeda, M., Okada, Y., Hagiwara, K. et al. A case of pulmonary sclerosing pneumocytoma in the hilar lesion. Gen Thorac Cardiovasc Surg 67, 818–820 (2019). https://doi.org/10.1007/s11748-018-1043-6
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DOI: https://doi.org/10.1007/s11748-018-1043-6