Ding Wenshuang, Wang Jianchao, Zhao Sha, Yang Qunpei, Sun Hong, Yan Jiaqi, Gao Limin, Yao Wenqing, Zhang Wenyan, Liu Weiping
Department of Pathology, West China Hospital of Sichuan University, Cheng Du, Sichuan 610041, China.
Department of Pathology, West China Hospital of Sichuan University, Cheng Du, Sichuan 610041, China.
Pathol Res Pract. 2015 Jul;211(7):544-9. doi: 10.1016/j.prp.2015.04.002. Epub 2015 Apr 17.
Malignant tumors of the lung are predominantly derived from epithelial tissue, such as squamous cell carcinoma and adenocarcinoma, while pulmonary lymphatic and hematopoietic tumor is relatively rare. Extranodal NK/T-cell lymphoma (ENKTL), nasal type, originates in nasal and extra-nasal sites anatomically. This distinct non-Hodgkin lymphoma is endemic and is characterized by a highly aggressive clinical course and dismal survival outcome. Extra-nasal ENKTL, especially pulmonary ENKTL, is rare compared with nasal type ENKTL and has received relatively little attention. Therefore, this study was conducted to assess the clinicopathological features of pulmonary ENKTL and to promote awareness of this malignancy.
All cases of ENKTL, nasal type diagnosed from January 2008 to June 2014 in our institution were collected, and those with pulmonary involvement were selected for further study. The eligible cases were analyzed retrospectively: medical recordings, imaging manifestations, pathological features, immunophenotypes, EBER1/2 hybridizations in situ and other related literatures were reviewed.
A total of 1105 cases were diagnosed as ENKTL, nasal type, in this period, and 8 cases (7.2‰) had lung involvement. Seven cases had core biopsy, and for 1 case, a resected tissue specimen was available. The group was composed of 6 men and 2 women (gender ratio 3:1) with ages ranging from 19 to 44 (average age of 33.5) years. In this group, 2 cases were secondary and 5 cases were primary. The clinical symptoms and computed tomography (CT) manifestations were nonspecific. Histologically, the neoplasms presented angiocentric and angiodestructive growth patterns with different degrees of inflammatory response and necrosis. The neoplastic cell sizes were heterogeneous with spectra of small to large or mixed-composition types. For the immunophenotypes, all cases were positive for CD3ɛ and cytotoxic granule (granzyme B or TIA-1). The positive ratios of CD56 and CD30 were 6/8 and 4/5 respectively. All 8 cases showed positive in situ hybridization for Epstein-Barr virus-encoded small RNA (EBER). TCR-γ gene rearrangement was tested in 4 cases, and only 1 of these cases was monoclonal. Laboratory testing demonstrated that the whole blood was decreased while the average level of LDH was elevated. Six bone marrow biopsy specimens were negative and showed no neoplastic cells infiltration. For treatment, 4 individuals accepted chemotherapy and 1 patient underwent localized tumor resection surgery. The follow-up information was available for 6 patients, 1 of whom was alive and the other 5 cases survived shortly between 20 days and 4 months. ENKTL, nasal type of lung is very rare, and the diagnosis is challenging due to nonspecific clinical symptoms and imaging results. The diagnosis of pulmonary ENKTL should be based on comprehensive clinical, imaging, histopathological and molecular examination. More effective treatment strategies are required for this disease.
肺恶性肿瘤主要起源于上皮组织,如鳞状细胞癌和腺癌,而肺淋巴造血系统肿瘤相对少见。结外NK/T细胞淋巴瘤(ENKTL),鼻型,在解剖学上起源于鼻腔及鼻外部位。这种独特的非霍奇金淋巴瘤具有地方性,临床病程高度侵袭性,生存结局不佳。与鼻型ENKTL相比,鼻外ENKTL,尤其是肺ENKTL较为罕见,受到的关注相对较少。因此,本研究旨在评估肺ENKTL的临床病理特征,提高对这种恶性肿瘤的认识。
收集2008年1月至2014年6月在我院诊断为鼻型ENKTL的所有病例,选取有肺部受累的病例进行进一步研究。对符合条件的病例进行回顾性分析:查阅病历记录、影像学表现、病理特征、免疫表型、原位EBER1/2杂交及其他相关文献。
在此期间共诊断出1105例鼻型ENKTL,其中8例(7.2‰)有肺部受累。7例进行了芯针活检,1例有切除的组织标本。该组由6名男性和2名女性组成(性别比3:1),年龄在19至44岁之间(平均年龄33.5岁)。该组中,2例为继发性,5例为原发性。临床症状和计算机断层扫描(CT)表现无特异性。组织学上,肿瘤呈血管中心性和血管破坏性生长模式,伴有不同程度的炎症反应和坏死。肿瘤细胞大小不一,有小至大或混合组成类型。免疫表型方面,所有病例CD3ɛ和细胞毒性颗粒(颗粒酶B或TIA-1)均为阳性。CD56和CD30的阳性率分别为6/8和4/5。8例均显示爱泼斯坦-巴尔病毒编码小RNA(EBER)原位杂交阳性。对4例进行了TCR-γ基因重排检测,其中仅1例为单克隆性。实验室检查显示全血减少,而乳酸脱氢酶平均水平升高。6例骨髓活检标本为阴性,未显示肿瘤细胞浸润。治疗方面,4例接受化疗,1例接受局部肿瘤切除手术。6例患者有随访信息,其中1例存活,其他5例在20天至4个月内短期内死亡。肺鼻型ENKTL非常罕见,由于临床症状和影像学结果无特异性,诊断具有挑战性。肺ENKTL的诊断应基于综合的临床、影像学、组织病理学和分子检查。对于这种疾病需要更有效的治疗策略。