Evidence map›Paper›PMID 41199912›Full record

ArticleCase reports in oncological medicine2025

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

Mohammed B Abboushi, Omar Marouf, Mohammed AbuBaha, Hossam Salameh, Ro'ya Soradi, Riad Ahmad Amer

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Article in Case reports in oncological medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Mohammed B AbboushiDepartment of Internal Medicine, An-Najah National University Hospital, Nablus, State of Palestine.
Omar MaroufDepartment of Internal Medicine, Palestine Medical Complex, Ramallah, State of Palestine.
Mohammed AbuBahaDepartment of Medicine, An-Najah National University, Nablus, State of Palestine.ORCID https://orcid.org/0009-0000-0873-8374
Hossam SalamehDepartment of Medicine, An-Najah National University, Nablus, State of Palestine.ORCID https://orcid.org/0009-0009-5346-9973
Ro'ya SoradiPathology Department, An-Najah National University Hospital, Nablus, State of Palestine.
Riad Ahmad AmerOncology and Hematology Department, An-Najah National University Hospital, Nablus, State of Palestine.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Identifiers

PMID41199912
PMCPMC12588754

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