Lee Hyun Soo, Kim Jina, Moon Duk Hwan, Park Chul Hwan, Jeon Tae Joo, Lee Sungsoo, Cha Yoon Jin
Department of Thoracic and Cardiovascular Surgery, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
Department of Radiology and the Research Institute of Radiological Science, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
J Chest Surg. 2021 Dec 5;54(6):528-531. doi: 10.5090/jcs.21.016.
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.
肺硬化性肺细胞瘤(PSP)是一种起源于肺上皮细胞的肿瘤,被归类为良性肿瘤。迄今为止,该肿瘤的侵袭性行为鲜有报道。在此,我们描述了一例56岁女性患者,其患有一个巨大的19厘米的PSP,导致纵隔移位,并显示有镜下支气管内侵犯和坏死。鉴别诊断包括恶性间叶性肿瘤,如孤立性纤维瘤;然而,通过肿瘤细胞免疫组化染色显示特征性的甲状腺转录因子1阳性和Ki-67的膜表达,确诊为PSP。