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复合淋巴瘤的临床病理分析:两例报告及文献复习

Clinicopathological analysis of composite lymphoma: A two-case report and literature review.

作者信息

Gui Wei, Wang Jing, Ma Li, Wang Yanli, Su Liping

机构信息

Department of Hematology, Shanxi Tumor Hospital, Taiyuan, Shanxi, People's Republic of China.

Department of Pathology, Shanxi Tumor Hospital, Taiyuan, Shanxi 030013, People's Republic of China.

出版信息

Open Med (Wars). 2020 Jul 10;15(1):654-658. doi: 10.1515/med-2020-0191. eCollection 2020.

Abstract

OBJECTIVE

The objective of this study was to evaluate the clinicopathological features and treatment of composite lymphoma (CL) with cervical lymph node enlargement.

METHODS

In this study, two cases of CL are presented. Biopsies of enlarged cervical lymph nodes by excision revealed two distinct types of lymphomas. The diagnoses were confirmed by routine histopathology, immunohistochemistry, hybridization, polymerase chain reactions and flow cytometry. Case 1 was diagnosed with Hodgkin's lymphoma and cytotoxic T-cell lymphoma complicated by Epstein-Barr virus infection. Case 2 was diagnosed with diffuse large B-cell lymphoma and angioimmunoblastic T-cell lymphoma.

RESULTS

Case 1 received one cycle of adriamycin, bleomycin, vincristine and dacarbazine (ABVD regimen) combined with chidamide, followed by one cycle of gemcitabine and dexamethasone (GDP regimen) combined with chidamide, and then oral acyclovir. The patient achieved stable disease, but was lost to follow-up. Case 2 received eight cycles of cyclophosphamide, pirarubicin, vincristine and dexamethasone (CTOP regimen) combined with chidamide, and the patient achieved complete remission. Nine months later, relapse was confirmed. She received chidamide monotherapy for 3 months, which was then terminated. One year later, the patient underwent progressive disease and died.

CONCLUSIONS

CL is a kind of rare disease. Due to the complexity of CL, clinicians should consider both disease components in order to increase the likelihood of effective treatment. This is important.

摘要

目的

本研究旨在评估伴有颈部淋巴结肿大的复合淋巴瘤(CL)的临床病理特征及治疗情况。

方法

本研究报告了2例CL病例。通过切除肿大的颈部淋巴结进行活检,发现了两种不同类型的淋巴瘤。通过常规组织病理学、免疫组织化学、杂交、聚合酶链反应和流式细胞术确诊。病例1被诊断为霍奇金淋巴瘤和细胞毒性T细胞淋巴瘤合并爱泼斯坦-巴尔病毒感染。病例2被诊断为弥漫性大B细胞淋巴瘤和血管免疫母细胞性T细胞淋巴瘤。

结果

病例1接受了一个周期的阿霉素、博来霉素、长春新碱和达卡巴嗪(ABVD方案)联合西达本胺治疗,随后接受了一个周期的吉西他滨和地塞米松(GDP方案)联合西达本胺治疗,然后口服阿昔洛韦。患者病情稳定,但失访。病例2接受了八个周期的环磷酰胺、吡柔比星、长春新碱和地塞米松(CTOP方案)联合西达本胺治疗,患者达到完全缓解。九个月后,证实复发。她接受了3个月的西达本胺单药治疗,随后终止。一年后,患者病情进展并死亡。

结论

CL是一种罕见疾病。由于CL的复杂性,临床医生应考虑两种疾病成分,以提高有效治疗的可能性。这很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51ed/7712032/6f8caa6ba5ff/j_med-2020-0191-fig001.jpg

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