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复合性 B 细胞和 T 细胞淋巴瘤:三例病例的临床、病理和分子特征及文献复习。

Composite B-cell and T-cell lymphomas: clinical, pathological, and molecular features of three cases and literature review.

机构信息

Department of Hematology, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China.

Department of Pathology, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China.

出版信息

J Zhejiang Univ Sci B. 2023 Aug 15;24(8):711-722. doi: 10.1631/jzus.B2300181.

Abstract

Composite lymphoma (CL) involving B-cell lymphoma and T-cell lymphoma is extremely rare. Herein, we report three such cases using immunohistochemistry, flow cytometry, and the next-generation sequencing (NGS) to identify the pathological and molecular characteristics of CL. In the first case, the patient was admitted to hospital for generalized pruritic maculopapular rash over the whole body. An excisional biopsy of the skin lesions showed T-cell lymphoma. At the same time, the staging bone marrow (BM) biopsy revealed a diffuse large B-cell lymphoma (DLBCL). After R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone) therapies, the patient produced a good response with substantial dissipation of the rashes and relief of skin. The other two patients were admitted to hospital due to lymphadenopathy and were diagnosed with DLBCL and follicular lymphoma (FL) after core needle biopsy of lymph nodes, BM biopsy, BM aspiration, and flow cytometry. Following R-CHOP and R-COP (rituximab, cyclophosphamide, vincristine, and prednisone) therapies, they achieved complete remission unconfirmed (CRu) and complete remission (CR). However, one or two years later, they suffered a relapse of lymphadenopathy. The shocking fact was that re-biopsy of lymphadenopathy revealed peripheral T-cell lymphoma (PTCL) and angioimmunoblastic T-cell lymphoma (AITL). NGS findings identified DNA methyltransferase 3a (), isocitrate dehydrogenase 2 (), Ras homolog gene family, member A (), splicing factor 3B subunit 1 (), and tumor protein p53 () mutations. After immunochemotherapy, these patients achieved CRu and CR again. Nevertheless, they suffered a second relapse of T-cell lymphoma. Finally, they died due to progression of disease. We found that the occurrence of CL is associated with Epstein-Barr virus infection and , , and mutations, and the prognosis of the disease is closely related to the T-cell lymphoma components.

摘要

复合淋巴瘤(CL)涉及 B 细胞淋巴瘤和 T 细胞淋巴瘤极为罕见。本文通过免疫组化、流式细胞术和下一代测序(NGS)报道了三例此类病例,以鉴定 CL 的病理和分子特征。在第一个病例中,患者因全身广泛瘙痒性斑丘疹入院。皮肤病变的切除活检显示 T 细胞淋巴瘤。同时,分期骨髓(BM)活检显示弥漫性大 B 细胞淋巴瘤(DLBCL)。在接受 R-CHOP(利妥昔单抗、环磷酰胺、多柔比星、长春新碱和泼尼松)治疗后,患者反应良好,皮疹大量消散,皮肤症状缓解。另外两例患者因淋巴结肿大入院,经淋巴结核心针活检、BM 活检、BM 抽吸和流式细胞术诊断为 DLBCL 和滤泡性淋巴瘤(FL)。接受 R-CHOP 和 R-COP(利妥昔单抗、环磷酰胺、长春新碱和泼尼松)治疗后,他们达到完全缓解未确认(CRu)和完全缓解(CR)。然而,一到两年后,他们再次出现淋巴结病复发。令人震惊的事实是,淋巴结病的再次活检显示外周 T 细胞淋巴瘤(PTCL)和血管免疫母细胞性 T 细胞淋巴瘤(AITL)。NGS 结果发现 DNA 甲基转移酶 3a()、异柠檬酸脱氢酶 2()、Ras 同源基因家族成员 A()、剪接因子 3B 亚基 1()和肿瘤蛋白 p53()突变。经过免疫化疗,这些患者再次达到 CRu 和 CR。然而,他们又经历了第二次 T 细胞淋巴瘤复发。最终,他们因疾病进展而死亡。我们发现 CL 的发生与 Epstein-Barr 病毒感染以及、、和突变有关,疾病的预后与 T 细胞淋巴瘤成分密切相关。

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