Fang Yixuan, Wang Anzhe, Shen Lumin, Yuan Xiao, Kong Yu
Department of Pathology, the First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Zhongguo Fei Ai Za Zhi. 2024 Nov 20;27(11):840-848. doi: 10.3779/j.issn.1009-3419.2024.101.29.
Primary pulmonary lymphoepithelial carcinoma (PPLEC) is a rare form of lung malignancy, accounting for only 0.7% of all lung cancers. It is currently classified as a distinct subtype within squamous cell carcinomas. This study aims to explore the clinicopathological characteristics of PPLEC and its subtypes, with the objective of enhancing understanding and improving diagnostic accuracy for this disease.
A retrospective analysis was conducted on the clinical, pathological, imaging, and prognostic data of 14 patients diagnosed with PPLEC at the First Affiliated Hospital of Soochow University between February 2019 and June 2023.
A total of 14 cases of PPLEC were identified, including 5 cases of the Regaud type, with ages ranging from 33 to 73 years, comprising 2 males and 3 females; and 9 cases of the Schmincke type, with ages ranging from 36 to 79 years, including 4 males and 5 females. Computed tomography (CT) scans consistently demonstrated soft tissue masses or nodular shadows. Reagud type mainly showed peripheral masses and Schmincke type mainly showed central masses. Pathological examination revealed tumor cells exhibiting syncytial-like growth, accompanied by lymphocytic infiltration and stromal fibrosis, with the Regaud type showing well-defined borders combined with granulomatous inflammation, while the Schmincke type exhibited indistinct tumor margins. Immunohistochemistry showed that CK, CK5/6, P40 and P63 were positive, and the Ki-67 index of Regaud type was lower than that of Schmincke type; notably, all 8 cases tested for programmed death-ligand 1 (PD-L1) were positive. Epstein-Barr virus-encoded RNA (EBER) in situ hybridization was positive in all instances. Among these cases, 6 underwent surgical treatment, and 8 received comprehensive therapy; by the end of the follow-up period, all 14 patients remained alive.
PPLEC is a rare form of malignant lung tumor associated with Epstein-Barr virus (EBV) infection. The Regaud and Schmincke subtypes display distinct imaging and pathological characteristics. In the early stages of the disease, surgical intervention is the primary treatment method; however, for advanced stages, a multimodal treatment approach is utilized, resulting in a relatively favorable prognosis. Immunotherapy represents a promising and effective treatment modality for patients with middle to advanced stage disease exhibiting high PD-L1 expression levels.
原发性肺淋巴上皮癌(PPLEC)是一种罕见的肺恶性肿瘤,仅占所有肺癌的0.7%。目前它被归类为鳞状细胞癌中的一个独特亚型。本研究旨在探讨PPLEC及其亚型的临床病理特征,以增进对该疾病的了解并提高诊断准确性。
对2019年2月至2023年6月期间在苏州大学附属第一医院确诊为PPLEC的14例患者的临床、病理、影像和预后数据进行回顾性分析。
共确诊14例PPLEC,其中雷高德型5例,年龄33至73岁,男性2例,女性3例;施密克型9例,年龄36至79岁,男性4例,女性5例。计算机断层扫描(CT)始终显示软组织肿块或结节状阴影。雷高德型主要表现为周围型肿块,施密克型主要表现为中央型肿块。病理检查显示肿瘤细胞呈合体样生长,伴有淋巴细胞浸润和间质纤维化,雷高德型边界清晰并伴有肉芽肿性炎症,而施密克型肿瘤边界不清。免疫组化显示细胞角蛋白(CK)、CK5/6、P40和P63呈阳性,雷高德型的Ki-67指数低于施密克型;值得注意的是,所有检测程序性死亡配体1(PD-L1)的8例均为阳性。爱泼斯坦-巴尔病毒编码RNA(EBER)原位杂交在所有病例中均为阳性。其中6例接受了手术治疗,8例接受了综合治疗;至随访期末,14例患者均存活。
PPLEC是一种与爱泼斯坦-巴尔病毒(EBV)感染相关的罕见肺恶性肿瘤。雷高德型和施密克型亚型表现出不同的影像和病理特征。在疾病早期,手术干预是主要治疗方法;然而,对于晚期患者,则采用多模式治疗方法,预后相对良好。免疫治疗对于中晚期且PD-L1表达水平高的患者是一种有前景且有效的治疗方式。