Manas Dave, Lucia Lazzereschi, Muntasser Alsharabati, Ke Xu, Teresa Marafioti
{"title":"cd5阳性毛细胞白血病","authors":"Manas Dave, Lucia Lazzereschi, Muntasser Alsharabati, Ke Xu, Teresa Marafioti","doi":"10.1016/j.mpdhp.2025.07.007","DOIUrl":null,"url":null,"abstract":"<div><div>Hairy cell leukaemia (HCL) is readily recognized by its distinct clinical presentation (cytopenias, splenomegaly and neoplastic cells with hair-like cytoplasmic projections), characteristic immunophenotype and <em>BRAF</em> p.V600E mutation. They are typically negative for CD5, CD10 and CD23. Rare cases, however, can have aberrant expression of CD5 and/or CD23 which can be confused with chronic lymphocytic leukaemia/small lymphocytic leukaemia (CD5+/CD23+) or mantle cell lymphoma/leukaemia (CD5+/Cyclin D1+). We describe a rare case of HCL with aberrant expression of CD5 that illustrates the importance of clinical, morphological, immunophenotypical and molecular investigations to resolve the diagnostic challenge.</div></div>","PeriodicalId":39961,"journal":{"name":"Diagnostic Histopathology","volume":"31 10","pages":"Pages 650-654"},"PeriodicalIF":0.0000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"CD5-positive hairy cell leukaemia\",\"authors\":\"Manas Dave, Lucia Lazzereschi, Muntasser Alsharabati, Ke Xu, Teresa Marafioti\",\"doi\":\"10.1016/j.mpdhp.2025.07.007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Hairy cell leukaemia (HCL) is readily recognized by its distinct clinical presentation (cytopenias, splenomegaly and neoplastic cells with hair-like cytoplasmic projections), characteristic immunophenotype and <em>BRAF</em> p.V600E mutation. They are typically negative for CD5, CD10 and CD23. Rare cases, however, can have aberrant expression of CD5 and/or CD23 which can be confused with chronic lymphocytic leukaemia/small lymphocytic leukaemia (CD5+/CD23+) or mantle cell lymphoma/leukaemia (CD5+/Cyclin D1+). We describe a rare case of HCL with aberrant expression of CD5 that illustrates the importance of clinical, morphological, immunophenotypical and molecular investigations to resolve the diagnostic challenge.</div></div>\",\"PeriodicalId\":39961,\"journal\":{\"name\":\"Diagnostic Histopathology\",\"volume\":\"31 10\",\"pages\":\"Pages 650-654\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Diagnostic Histopathology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1756231725001306\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Diagnostic Histopathology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1756231725001306","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Hairy cell leukaemia (HCL) is readily recognized by its distinct clinical presentation (cytopenias, splenomegaly and neoplastic cells with hair-like cytoplasmic projections), characteristic immunophenotype and BRAF p.V600E mutation. They are typically negative for CD5, CD10 and CD23. Rare cases, however, can have aberrant expression of CD5 and/or CD23 which can be confused with chronic lymphocytic leukaemia/small lymphocytic leukaemia (CD5+/CD23+) or mantle cell lymphoma/leukaemia (CD5+/Cyclin D1+). We describe a rare case of HCL with aberrant expression of CD5 that illustrates the importance of clinical, morphological, immunophenotypical and molecular investigations to resolve the diagnostic challenge.
期刊介绍:
This monthly review journal aims to provide the practising diagnostic pathologist and trainee pathologist with up-to-date reviews on histopathology and cytology and related technical advances. Each issue contains invited articles on a variety of topics from experts in the field and includes a mini-symposium exploring one subject in greater depth. Articles consist of system-based, disease-based reviews and advances in technology. They update the readers on day-to-day diagnostic work and keep them informed of important new developments. An additional feature is the short section devoted to hypotheses; these have been refereed. There is also a correspondence section.