Tadeusz Robak, Agnieszka Pluta, Pawel Robak, Agnieszka Janus, Ewa Wawrzyniak, Marcin Braun
{"title":"Burkitt lymphoma in patients with chronic lymphocytic leukemia and other indolent B-cell lymphoid malignancies.","authors":"Tadeusz Robak, Agnieszka Pluta, Pawel Robak, Agnieszka Janus, Ewa Wawrzyniak, Marcin Braun","doi":"10.1080/10428194.2025.2475337","DOIUrl":null,"url":null,"abstract":"<p><p>The most common form of Richter transformation, observed in 90-95% of patients, is the transformation of chronic lymphocytic leukemia (CLL) into diffuse large B-cell lymphoma (DLBCL). CLL has also been found to transform into Hodgkin lymphoma, prolymphocytic leukemia, and, in extremely rare cases, into other hematological malignancies, including Burkitt lymphoma (BL). This manuscript discusses a case of CLL transforming into BL and reviews a rare collection of cases of Burkitt lymphoma or Burkitt-like lymphoma associated with CLL,B-cell prolymphocytic leukemia, mantle cell lymphoma, follicular lymphoma, lymphoplasmacytic lymphoma and splenic marginal zone lymphoma. It covers the pathogenesis, prognosis, clinical characteristics, and treatment outcomes of Burkitt transformation in CLL and other indolent B-cell lymphoid malignancies patients. A comprehensive search was conducted using PubMed, Web of Science, and Google Scholar for articles published between January 1980 and December 2024 on chronic lymphocytic leukemia, Burkitt lymphoma, indolent lymphoma, mantle cell lymphoma, follicular lymphoma, marginal zone lymphoma, 8q24/MYC rearrangement, Epstein-Barr virus-positive lymphoma, and translocation t(8;14)(q24;q32). Additional relevant publications were identified by reviewing the references cited in the selected articles.</p>","PeriodicalId":18047,"journal":{"name":"Leukemia & Lymphoma","volume":" ","pages":"1376-1388"},"PeriodicalIF":2.2000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Leukemia & Lymphoma","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/10428194.2025.2475337","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/25 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The most common form of Richter transformation, observed in 90-95% of patients, is the transformation of chronic lymphocytic leukemia (CLL) into diffuse large B-cell lymphoma (DLBCL). CLL has also been found to transform into Hodgkin lymphoma, prolymphocytic leukemia, and, in extremely rare cases, into other hematological malignancies, including Burkitt lymphoma (BL). This manuscript discusses a case of CLL transforming into BL and reviews a rare collection of cases of Burkitt lymphoma or Burkitt-like lymphoma associated with CLL,B-cell prolymphocytic leukemia, mantle cell lymphoma, follicular lymphoma, lymphoplasmacytic lymphoma and splenic marginal zone lymphoma. It covers the pathogenesis, prognosis, clinical characteristics, and treatment outcomes of Burkitt transformation in CLL and other indolent B-cell lymphoid malignancies patients. A comprehensive search was conducted using PubMed, Web of Science, and Google Scholar for articles published between January 1980 and December 2024 on chronic lymphocytic leukemia, Burkitt lymphoma, indolent lymphoma, mantle cell lymphoma, follicular lymphoma, marginal zone lymphoma, 8q24/MYC rearrangement, Epstein-Barr virus-positive lymphoma, and translocation t(8;14)(q24;q32). Additional relevant publications were identified by reviewing the references cited in the selected articles.
期刊介绍:
Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor