Pulmonary sclerosing pneumocytoma (PSP) is a rare and interesting pulmonary tumour that presents a diagnostic challenge to the surgeon due to its bland symptomatology, indolent course, non-specific radiological features and ambiguous histopathological findings, which could lead to errors in management and prognostication. Herein, we present a series of 4 patients with PSP who were managed in our institution over a period of 8 years and briefly discuss relevant literature.
Keywords: Benign or congenital lesions; Carcinoid; Immunohistochemistry; Lung; Sclerosing pneumocytoma; Tumour.
© Indian Association of Cardiovascular-Thoracic Surgeons 2021.