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- Publisher Website: 10.1016/j.humpath.2004.04.002
- Scopus: eid_2-s2.0-3142634593
- PMID: 15257558
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Article: Transformation of diffuse large B-cell lymphoma into pre-B acute lymphoblastic leukemia: Clinicopathologic features and clonal relationship
Title | Transformation of diffuse large B-cell lymphoma into pre-B acute lymphoblastic leukemia: Clinicopathologic features and clonal relationship |
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Authors | |
Keywords | acute lymphoblastic leukemia ALL clonal evolution diffuse large B-cell lymphoma DLBC EBER Epstein-Barr virus-expressed RNA IgH immunoglobulin heavy chain PCR polymerase chain reaction Tdt |
Issue Date | 2004 |
Publisher | WB Saunders Co. The Journal's web site is located at http://www.elsevier.com/locate/humpath |
Citation | Human Pathology, 2004, v. 35 n. 7, p. 900-903 How to Cite? |
Abstract | A patient with fibrosing alveolitis developed a diffuse large B-cell (DLBC) lymphoma that expressed CD20 and CD30. After an initial response, the lymphoma relapsed and was salvaged with further chemotherapy. After another remission of 3 years, a pre-B-cell acute lymphoblastic leukemia (ALL), which expressed CD10, CD19, CD22, CD79a, CD34 and terminal deoxyribonucleotidyl transferase, developed and led to death. Molecular analysis of the immunoglobulin heavy-chain gene showed that the initial lymphoma and its relapse were clonally related. At leukemic relapse, 2 clones related to the initial and relapsed lymphoma clones were present. DLBC lymphomas arise from post-follicle center B cells, whereas ALL arises from pregerminal B cells. Therefore, a direct transformation of DLBC lymphoma to ALL appears unlikely. The overall features suggest instead separate lymphoma and leukemic evolution from a common mutated B-cell precursor rather than transformation of DLBC lymphoma to ALL. © 2004 Elsevier Inc. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/77072 |
ISSN | 2023 Impact Factor: 2.7 2023 SCImago Journal Rankings: 0.936 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Au, WY | en_HK |
dc.contributor.author | Srivastava, G | en_HK |
dc.contributor.author | Wong, KY | en_HK |
dc.contributor.author | Chung, LP | en_HK |
dc.contributor.author | Ma, SK | en_HK |
dc.contributor.author | Wan, TS | en_HK |
dc.contributor.author | Kwong, YL | en_HK |
dc.date.accessioned | 2010-09-06T07:27:58Z | - |
dc.date.available | 2010-09-06T07:27:58Z | - |
dc.date.issued | 2004 | en_HK |
dc.identifier.citation | Human Pathology, 2004, v. 35 n. 7, p. 900-903 | en_HK |
dc.identifier.issn | 0046-8177 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/77072 | - |
dc.description.abstract | A patient with fibrosing alveolitis developed a diffuse large B-cell (DLBC) lymphoma that expressed CD20 and CD30. After an initial response, the lymphoma relapsed and was salvaged with further chemotherapy. After another remission of 3 years, a pre-B-cell acute lymphoblastic leukemia (ALL), which expressed CD10, CD19, CD22, CD79a, CD34 and terminal deoxyribonucleotidyl transferase, developed and led to death. Molecular analysis of the immunoglobulin heavy-chain gene showed that the initial lymphoma and its relapse were clonally related. At leukemic relapse, 2 clones related to the initial and relapsed lymphoma clones were present. DLBC lymphomas arise from post-follicle center B cells, whereas ALL arises from pregerminal B cells. Therefore, a direct transformation of DLBC lymphoma to ALL appears unlikely. The overall features suggest instead separate lymphoma and leukemic evolution from a common mutated B-cell precursor rather than transformation of DLBC lymphoma to ALL. © 2004 Elsevier Inc. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | WB Saunders Co. The Journal's web site is located at http://www.elsevier.com/locate/humpath | en_HK |
dc.relation.ispartof | Human Pathology | en_HK |
dc.subject | acute lymphoblastic leukemia | en_HK |
dc.subject | ALL | en_HK |
dc.subject | clonal evolution | en_HK |
dc.subject | diffuse large B-cell lymphoma | en_HK |
dc.subject | DLBC | en_HK |
dc.subject | EBER | en_HK |
dc.subject | Epstein-Barr virus-expressed RNA | en_HK |
dc.subject | IgH | en_HK |
dc.subject | immunoglobulin heavy chain | en_HK |
dc.subject | PCR | en_HK |
dc.subject | polymerase chain reaction | en_HK |
dc.subject | Tdt | en_HK |
dc.subject.mesh | Aged | en_HK |
dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | en_HK |
dc.subject.mesh | Base Sequence | en_HK |
dc.subject.mesh | Burkitt Lymphoma - drug therapy - genetics - pathology | en_HK |
dc.subject.mesh | Cell Transformation, Neoplastic - genetics - pathology | en_HK |
dc.subject.mesh | Clone Cells | en_HK |
dc.subject.mesh | DNA, Neoplasm - analysis | en_HK |
dc.subject.mesh | Fatal Outcome | en_HK |
dc.subject.mesh | Female | en_HK |
dc.subject.mesh | Humans | en_HK |
dc.subject.mesh | Immunophenotyping | en_HK |
dc.subject.mesh | In Situ Hybridization | en_HK |
dc.subject.mesh | Karyotyping | en_HK |
dc.subject.mesh | Lymphoma, B-Cell - drug therapy - genetics - pathology | en_HK |
dc.subject.mesh | Lymphoma, Large B-Cell, Diffuse - drug therapy - genetics - pathology | en_HK |
dc.subject.mesh | Molecular Sequence Data | en_HK |
dc.subject.mesh | Neoplasms, Second Primary | en_HK |
dc.subject.mesh | RNA, Neoplasm - analysis | en_HK |
dc.subject.mesh | RNA, Viral - analysis | en_HK |
dc.subject.mesh | RNA-Binding Proteins - analysis | en_HK |
dc.subject.mesh | Ribosomal Proteins - analysis | en_HK |
dc.title | Transformation of diffuse large B-cell lymphoma into pre-B acute lymphoblastic leukemia: Clinicopathologic features and clonal relationship | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0046-8177&volume=35&issue=7&spage=900&epage=903&date=2004&atitle=Transformation+of+diffuse+large+B-cell+lymphoma+into+pre-B+acute+lymphoblastic+leukemia:+clinicopathologic+features+and+clonal+relationship | en_HK |
dc.identifier.email | Srivastava, G: sgopesh@hkucc.hku.hk | en_HK |
dc.identifier.email | Chung, LP: lpchung@hkucc.hku.hk | en_HK |
dc.identifier.email | Kwong, YL: ylkwong@hku.hk | en_HK |
dc.identifier.authority | Srivastava, G=rp00365 | en_HK |
dc.identifier.authority | Chung, LP=rp00249 | en_HK |
dc.identifier.authority | Kwong, YL=rp00358 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.humpath.2004.04.002 | en_HK |
dc.identifier.pmid | 15257558 | - |
dc.identifier.scopus | eid_2-s2.0-3142634593 | en_HK |
dc.identifier.hkuros | 94891 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-3142634593&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 35 | en_HK |
dc.identifier.issue | 7 | en_HK |
dc.identifier.spage | 900 | en_HK |
dc.identifier.epage | 903 | en_HK |
dc.identifier.isi | WOS:000223052900021 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Au, WY=7202383089 | en_HK |
dc.identifier.scopusauthorid | Srivastava, G=7202242238 | en_HK |
dc.identifier.scopusauthorid | Wong, KY=7404758500 | en_HK |
dc.identifier.scopusauthorid | Chung, LP=24315879100 | en_HK |
dc.identifier.scopusauthorid | Ma, SK=37020910400 | en_HK |
dc.identifier.scopusauthorid | Wan, TS=25623981600 | en_HK |
dc.identifier.scopusauthorid | Kwong, YL=7102818954 | en_HK |
dc.identifier.issnl | 0046-8177 | - |