Lee Kang-Lung, Wu Mei-Han, Jhang Ying-Yu, Chen Chun-Ku, Yen Yi-Chen, Chen Yi-Chun
Department of Radiology, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.
School of Medicine, National Yang-Ming University, Taipei, Taiwan, ROC.
J Chin Med Assoc. 2020 Oct;83(10):936-942. doi: 10.1097/JCMA.0000000000000363.
Primary pulmonary lymphoepithelioma-like carcinoma (LELC) is a rare subtype of lung cancer. Both small-cell lung cancer (SCLC) and LELC often manifest as a centrally located tumor with lymphadenopathy. This retrospective study investigated and compared the initial computed tomography (CT) features and subsequent survival outcomes of LELC and SCLC.
A total of 50 patients with a confirmed diagnosis of LELC were enrolled and matched at a ratio of 1:1 with patients with SCLC according to the tumor stage. Utilizing a consensus approach, two radiologists reviewed pretreatment CT images. Survival outcomes were analyzed.
Well-defined tumors were significantly more common in the LELC group (LELC: 42% vs SCLC: 24%, p = 0.005). Based on the comparisons of the primary tumor with the muscles, LELC tumors exhibited a significantly higher percentage of attenuation on contrast-enhanced CT scans (21.6% ± 29% vs -14.2% ± 37%, p < 0.001). The prevalence of vascular or bronchial encasement (18% vs 40%, p = 0.028), background emphysematous changes (10% vs 60%, p < 0.001), and tumors located in upper lobes (18% vs 64%, p < 0.001) was significantly lower in the LELC group. Female gender (70% vs 12%, p < 0.001), younger age (57.6 ± 12.0 years vs 68.0 ± 11.0 years, p < 0.001), and without a history of smoking (16% vs 88%, p < 0.001) were factors more commonly found in the LELC group. The patients with LELC had a better prognosis with significantly longer median survival than did the patients with SCLC (23.4 months vs 17.3 months, p = 0.01).
Because SCLC demonstrated a more aggressive disease progression, differentiating LELC from SCLC is crucial. In Epstein-Barr virus-endemic areas, the diagnosis of LELC should be considered when approaching a patient with the above-mentioned CT and clinical features.
原发性肺淋巴上皮瘤样癌(LELC)是肺癌的一种罕见亚型。小细胞肺癌(SCLC)和LELC通常都表现为中心型肿瘤并伴有淋巴结病。本回顾性研究调查并比较了LELC和SCLC的初始计算机断层扫描(CT)特征及后续生存结果。
共纳入50例确诊为LELC的患者,并根据肿瘤分期按1:1的比例与SCLC患者进行匹配。采用一致的方法,两名放射科医生对治疗前的CT图像进行了评估。分析了生存结果。
边界清晰的肿瘤在LELC组中明显更为常见(LELC:42% vs SCLC:24%,p = 0.005)。通过将原发肿瘤与肌肉进行比较,LELC肿瘤在增强CT扫描上的强化百分比显著更高(21.6%±29% vs -14.2%±37%,p < 0.001)。血管或支气管包绕(18% vs 40%,p = 0.028)、背景肺气肿改变(10% vs 60%,p < 0.001)以及位于上叶的肿瘤(18% vs 64%,p < 0.001)在LELC组中的发生率显著更低。女性(70% vs 12%,p < 0.001)、年龄较轻(57.6±12.0岁 vs 68.0±11.0岁,p < 0.001)以及无吸烟史(16% vs 88%,p < 0.001)是LELC组中更常见的因素。LELC患者的预后较好,中位生存期明显长于SCLC患者(23.4个月 vs 17.3个月,p = 0.01)。
由于SCLC表现出更具侵袭性的疾病进展,因此区分LELC与SCLC至关重要。在爱泼斯坦 - 巴尔病毒流行地区,当遇到具有上述CT和临床特征的患者时,应考虑LELC的诊断。