J Chest Surg.  2021 Dec;54(6):528-531. 10.5090/jcs.21.016.

Huge Pulmonary Sclerosing Pneumocytoma with Endobronchial Invasion: A Case Report with a Literature Review

Affiliations
  • 1Departments of Thoracic and Cardiovascular Surgery, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea
  • 2Departments of Radiology and the Research Institute of Radiological Science, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea
  • 3Departments of Nuclear medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea
  • 4Departments of Pathology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea

Abstract

Pulmonary sclerosing pneumocytoma (PSP) is a tumor of pneumocytic origin that is classified as a benign neoplasm. To date, aggressive behavior of this tumor has rarely been reported. Here, we describe a case of a 56-year-old woman with a huge, 19-cm PSP that resulted in mediastinal shift and showed microscopic endobronchial invasion and necrosis. The differential diagnosis included malignant mesenchymal tumors, such as solitary fibrous tumor; however, PSP was confirmed based on the characteristic thyroid transcription factor 1 positivity and membranous expression of Ki-67 on immunohistochemical staining of tumor cells.

Keyword

Pulmonary sclerosing hemangioma; Computed tomography; Immunohistochemistry; Case report
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