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突尼斯结外NK/T细胞淋巴瘤:临床病理特征、免疫表型及EB病毒感染

Extranodal NK/T-cell lymphoma in Tunisia: clinicopathological features, immunophenotype and EBV infection.

作者信息

Missaoui Nabiha, Mestiri Sarra, Bouriga Aida, Abdessayed Nihed, Belakhdher Mouna, Ghammem Monia, Abdelkefi Mohamed, Mokni Moncef, Hmissa Sihem

机构信息

Research Unit UR14ES17, Medicine Faculty of Sousse, University of Sousse, Sousse, Tunisia.

Pathology Department, Farhet Hached Hospital, Sousse, Tunisia.

出版信息

J Egypt Natl Canc Inst. 2019 Oct 22;31(1):1. doi: 10.1186/s43046-019-0002-3.

Abstract

BACKGROUND

Extranodal NK/T-cell lymphomas (ENKTL) are rare non-Hodgkin's lymphomas with aggressive clinical behavior. ENKTL are frequently associated with the Epstein-Barr virus (EBV). Data on ENKTL in Africa and Arab world are extremely limited. The study investigated the clinicopathological characteristics, EBV infection, and immunophenotype of ENKTL in Tunisia. We conducted a retrospective study of ENKTL. Main clinicopathological features were reported. The expression of CD3, CD4, CD5, CD8, CD20, CD56, CD57, and Granzyme B were analyzed by immunohistochemistry. EBV infection was detected by IHC (LMP-1) and Epstein-Barr encoding region (EBER1/2) in situ hybridization.

RESULTS

A total of nine ENKTL were identified (mean age of 48 years and male-to-female ratio of 8:1). There were five nasal ENKTL, and the remaining four cases had extranasal involvement (palate, sub-mandibular gland, skin, and soft tissues of the ankle). The histopathology showed a lymphoid and pleomorphic proliferation characterized by images of angiocentrism. Strong and diffuse CD3 expression was observed in all cases. Tumor cells exhibited an expression of CD5 (two cases), CD8 (three cases), CD56 (six cases), CD57 (three cases), and Granzyme B (eight cases). All ENKTL cases were EBV-associated. Overall 5-year survival rate was 57%. Although six ENKTL were diagnosed at early clinical stages, the prognosis was unfavorable and associated with patient death in three cases.

CONCLUSIONS

ENKTL are exceptional in Tunisia with unfavorable outcome. Histopathological diagnosis remains challenging in clinical practice. However, a careful histopathological examination combined with a correct interpretation of immunohistochemistry and in situ hybridization results refines the ENKTL diagnosis.

摘要

背景

结外NK/T细胞淋巴瘤(ENKTL)是一种罕见的非霍奇金淋巴瘤,具有侵袭性临床行为。ENKTL常与EB病毒(EBV)相关。非洲和阿拉伯世界关于ENKTL的数据极为有限。本研究调查了突尼斯ENKTL的临床病理特征、EBV感染及免疫表型。我们对ENKTL进行了一项回顾性研究。报告了主要临床病理特征。通过免疫组织化学分析CD3、CD4、CD5、CD8、CD20、CD56、CD57和颗粒酶B的表达。通过免疫组化(LMP-1)和EB病毒编码区(EBER1/2)原位杂交检测EBV感染。

结果

共鉴定出9例ENKTL(平均年龄48岁,男女比例为8:1)。其中5例为鼻型ENKTL,其余4例有鼻外受累(腭部、下颌下腺、皮肤和踝部软组织)。组织病理学显示以血管中心性图像为特征的淋巴样和多形性增殖。所有病例均观察到强而弥漫的CD3表达。肿瘤细胞表达CD5(2例)、CD8(3例)、CD56(6例)、CD57(3例)和颗粒酶B(8例)。所有ENKTL病例均与EBV相关。总体5年生存率为57%。尽管6例ENKTL在临床早期被诊断,但预后不佳,3例患者死亡。

结论

ENKTL在突尼斯较为罕见,预后不良。在临床实践中,组织病理学诊断仍然具有挑战性。然而,仔细的组织病理学检查结合对免疫组织化学和原位杂交结果的正确解读可完善ENKTL的诊断。

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