肺硬化性肺细胞瘤——一名白种女性的罕见诊断：病例报告及文献复习

Pulmonary sclerosing pneumocytoma - rare diagnosis in a Caucasian woman: case report and review of the literature.

作者信息

Gorman William, Shehata Monica, Bashir Mohamed Ryan, Zhang Yu Zhi, Wassilew Katharina, AlShammari Abdullah, Buderi Silviu, Jordan Simon

机构信息

University of Cambridge School of Clinical Medicine, Addenbrooke's Hospital, Cambridge CB2 0SP, UK.

Department of Thoracic Surgery, The Royal Brompton Hospital, London SW3 6NP, UK.

出版信息

JRSM Open. 2024 Jun 13;15(6):20542704231200394. doi: 10.1177/20542704231200394. eCollection 2024 Jun.

DOI:10.1177/20542704231200394

PMID:39091433

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11292696/

Abstract

Pulmonary sclerosing pneumocytoma (PSP) is a rare benign pulmonary tumour, most reported cases of PSP are from Eastern Asia, with a female to male ratio of 5:1, and average age at diagnosis in the 5 decade. We present the case of a 63-year-old Caucasian woman diagnosed with PSP who underwent a left lower lobe basal segmentectomy with systematic nodal dissection, performed via video assisted thoracic surgery (VATS).

摘要

肺硬化性细胞瘤（PSP）是一种罕见的良性肺肿瘤，大多数报道的PSP病例来自东亚，女性与男性比例为5:1，诊断时的平均年龄在50岁左右。我们报告一例63岁的白种女性被诊断为PSP，她通过电视辅助胸腔镜手术（VATS）进行了左下叶基底段切除术及系统性淋巴结清扫。