Transformation of Classical Hodgkin Lymphoma Into Non-Hodgkin Lymphoma: Three Case Reports From the West Bank.

IF 0.6 Q4 ONCOLOGY
Case Reports in Oncological Medicine Pub Date : 2025-10-29 eCollection Date: 2025-01-01 DOI:10.1155/crom/4802098
Mohammed B Abboushi, Omar Marouf, Mohammed AbuBaha, Hossam Salameh, Ro'ya Soradi, Riad Ahmad Amer
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引用次数: 0

Abstract

Background: Classical Hodgkin lymphoma (cHL) is a highly curable B-cell malignancy; though, rarely, it can transform into non-Hodgkin lymphoma (NHL), including diffuse large B-cell lymphoma (DLBCL), follicular lymphoma, or marginal zone lymphoma. Reports of such transformations remain limited in the literature.

Objective: The aim of this study is to describe the clinical course, histopathological findings, and outcomes of three patients with cHL who developed secondary NHL.

Results: Case 1 involved transformation from cHL to CD20+/CD30+ DLBCL following multiple lines of chemotherapy and autologous stem cell transplant, eventually resulting in progressive disease and death. Case 2 transformed into follicular lymphoma Grade 3a more than a year after cHL remission, with marrow infiltration managed conservatively pending systemic therapy. Case 3 presented with composite lymphoma at diagnosis (cHL and extranodal marginal zone lymphoma) and experienced indolent but recurrent disease involving the liver, requiring multiple rounds of chemoimmunotherapy.

Conclusion: Transformation of cHL into NHL, though rare, may occur years after initial treatment or concurrently at presentation. These cases underscore the importance of repeat biopsy in suspected relapses and highlight the clinical and pathological heterogeneity of such transformations. Our paper adds to the limited literature on this phenomenon and is the first of its kind reported from Palestine.

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经典霍奇金淋巴瘤向非霍奇金淋巴瘤的转变:西岸3例报告
背景:经典霍奇金淋巴瘤(cHL)是一种高度可治愈的b细胞恶性肿瘤;然而,很少,它可以转化为非霍奇金淋巴瘤(NHL),包括弥漫性大b细胞淋巴瘤(DLBCL),滤泡性淋巴瘤或边缘区淋巴瘤。关于这种转变的报道在文献中仍然有限。目的:本研究的目的是描述3例cHL并发继发性NHL的临床过程、组织病理学结果和结局。结果:病例1在多系化疗和自体干细胞移植后从cHL转化为CD20+/CD30+ DLBCL,最终导致疾病进展和死亡。病例2在cHL缓解一年多后转化为3a级滤泡性淋巴瘤,骨髓浸润保守管理,等待全身治疗。病例3在诊断时表现为复合淋巴瘤(cHL和结外边缘区淋巴瘤),并经历了累及肝脏的惰性但复发性疾病,需要多轮化学免疫治疗。结论:cHL转化为NHL,虽然罕见,但可能发生在初始治疗后数年或同时出现。这些病例强调了在怀疑复发时重复活检的重要性,并强调了这种转变的临床和病理异质性。我们的论文增加了对这一现象的有限文献,并且是首次从巴勒斯坦报道的此类文献。
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来源期刊
自引率
0.00%
发文量
11
审稿时长
16 weeks
期刊介绍: Case Reports in Oncological Medicine is a peer-reviewed, Open Access journal that publishes case reports and case series related to breast cancer, lung cancer, gastrointestinal cancer, skin cancer, head and neck cancer, paediatric oncology, neurooncology as well as genitourinary cancer.
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