Cai Li, Wang Ting, Jiang Lei, Yang Ping, Hu Jinchen, Jiang Jing
Department of Medicine, The Affiliated Yantai Yuhuangding Hospital of Qingdao University No. 20 East Yuhuangding Road, Yantai, Shandong, China.
Int J Clin Exp Pathol. 2020 Oct 1;13(10):2599-2607. eCollection 2020.
Sclerosing pneumocytoma (SP) is a rare and benign tumor predominantly occurring in Asian women, easily misdiagnosed by imaging and pathologic frozen diagnosis during surgery because of its diverse histomorphology (4 structures, 2 types of cells). It may form multiple tumors. When SP is combined with carcinoid, adenoma, or other tumors (although rare), diagnosis is more complicated. SP mixed with carcinoid tumor is rare. At present, only 4 cases have been reported in English literature. Here, we report a case of sclerosing pneumocytoma combined not only with carcinoid, but also with clear cell adenoma of the lung. The patient was a 52-year-old female and CT found a nodule in the middle lobe of the right lung. SP was not excluded by intraoperative frozen section diagnosis. The above 3 components formed a 1.4 cm nodule. The related literature is reviewed to strengthen the understanding of SP, and aid clinicopathological diagnosis.
硬化性肺细胞瘤(SP)是一种罕见的良性肿瘤,主要发生于亚洲女性,因其多样的组织形态学表现(4种结构、2种细胞类型),在手术过程中容易被影像学及病理冰冻诊断误诊。它可能形成多个肿瘤。当SP合并类癌、腺瘤或其他肿瘤时(尽管罕见),诊断会更加复杂。SP与类癌肿瘤混合的情况罕见。目前,英文文献中仅报道了4例。在此,我们报告1例不仅合并类癌,还合并肺透明细胞腺瘤的硬化性肺细胞瘤病例。患者为一名52岁女性,CT发现右肺中叶有一个结节。术中冰冻切片诊断未排除SP。上述3种成分形成了一个1.4厘米的结节。现回顾相关文献以加强对SP的认识,并辅助临床病理诊断。