Polymerase chain reaction-Based clonality analysis of cutaneous B-cell lymphoproliferative processes

Detalhes bibliográficos
Autor(a) principal: Melotti, Claudia Z
Data de Publicação: 2010
Outros Autores: Amary, Maria Fernanda Carriel, Sotto, Miriam Nacagami, Diss, Timothy, Sanches, Jose Antonio
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Clinics
Texto Completo: https://www.revistas.usp.br/clinics/article/view/18422
Resumo: INTRODUCTION: The differential diagnosis of B-cell lymphoproliferative processes remains a challenge for pathologists, dermatologists and oncologists, despite advances in histology, immunohistochemistry and molecular biology. OBJECTIVE: Evaluate aid and limitations of clonality analysis in the diagnosis of primary cutaneous B-cell lymphomas and B-cell pseudolymphomas. METHODS: This study included 29 cases of B-cell lymphoproliferative processes classified as primary cutaneous B-cell lymphomas (13), B-cell pseudolymphomas (6) and inconclusive cases (10) using histology and immunohistochemistry. The clonality analysis was performed by polymerase chain reaction analysis of immunoglobulin light chain and heavy chain rearrangements. RESULTS: DNA quality was shown to be generally poor; eight samples were inadequate for polymerase chain reaction analysis. The results showed monoclonality in eight of the primary cutaneous B-cell lymphomas and polyclonality in four of the B-cell pseudolymphomas. In addition, monoclonality was shown in two of the inconclusive cases by histology and immunohistochemistry, demonstrating the utility of polymerase chain reaction as an ancillary diagnostic tool for primary cutaneous B-cell lymphomas. DISCUSSION: The low quality DNA extracted from these cases demanded the use of an IgH protocol that yielded small fragments and IgK. Both methods used together improved detection. CONCLUSION: Use of the two protocols, immunoglobulin heavy chain FR3-trad and immunoglobulin light chain-Kappa Biomed protocols for clonality analysis improved diagnostic accuracy.
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spelling Polymerase chain reaction-Based clonality analysis of cutaneous B-cell lymphoproliferative processes Cutaneous lymphomaPolymerase chain reactionGene rearrangementClonalityB-cellLymphoproliferative processes INTRODUCTION: The differential diagnosis of B-cell lymphoproliferative processes remains a challenge for pathologists, dermatologists and oncologists, despite advances in histology, immunohistochemistry and molecular biology. OBJECTIVE: Evaluate aid and limitations of clonality analysis in the diagnosis of primary cutaneous B-cell lymphomas and B-cell pseudolymphomas. METHODS: This study included 29 cases of B-cell lymphoproliferative processes classified as primary cutaneous B-cell lymphomas (13), B-cell pseudolymphomas (6) and inconclusive cases (10) using histology and immunohistochemistry. The clonality analysis was performed by polymerase chain reaction analysis of immunoglobulin light chain and heavy chain rearrangements. RESULTS: DNA quality was shown to be generally poor; eight samples were inadequate for polymerase chain reaction analysis. The results showed monoclonality in eight of the primary cutaneous B-cell lymphomas and polyclonality in four of the B-cell pseudolymphomas. In addition, monoclonality was shown in two of the inconclusive cases by histology and immunohistochemistry, demonstrating the utility of polymerase chain reaction as an ancillary diagnostic tool for primary cutaneous B-cell lymphomas. DISCUSSION: The low quality DNA extracted from these cases demanded the use of an IgH protocol that yielded small fragments and IgK. Both methods used together improved detection. CONCLUSION: Use of the two protocols, immunoglobulin heavy chain FR3-trad and immunoglobulin light chain-Kappa Biomed protocols for clonality analysis improved diagnostic accuracy. Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2010-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/1842210.1590/S1807-59322010000100009Clinics; Vol. 65 No. 1 (2010); 53-60 Clinics; v. 65 n. 1 (2010); 53-60 Clinics; Vol. 65 Núm. 1 (2010); 53-60 1980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/18422/20485Melotti, Claudia ZAmary, Maria Fernanda CarrielSotto, Miriam NacagamiDiss, TimothySanches, Jose Antonioinfo:eu-repo/semantics/openAccess2012-05-23T11:22:12Zoai:revistas.usp.br:article/18422Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2012-05-23T11:22:12Clinics - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Polymerase chain reaction-Based clonality analysis of cutaneous B-cell lymphoproliferative processes
title Polymerase chain reaction-Based clonality analysis of cutaneous B-cell lymphoproliferative processes
spellingShingle Polymerase chain reaction-Based clonality analysis of cutaneous B-cell lymphoproliferative processes
Melotti, Claudia Z
Cutaneous lymphoma
Polymerase chain reaction
Gene rearrangement
Clonality
B-cell
Lymphoproliferative processes
title_short Polymerase chain reaction-Based clonality analysis of cutaneous B-cell lymphoproliferative processes
title_full Polymerase chain reaction-Based clonality analysis of cutaneous B-cell lymphoproliferative processes
title_fullStr Polymerase chain reaction-Based clonality analysis of cutaneous B-cell lymphoproliferative processes
title_full_unstemmed Polymerase chain reaction-Based clonality analysis of cutaneous B-cell lymphoproliferative processes
title_sort Polymerase chain reaction-Based clonality analysis of cutaneous B-cell lymphoproliferative processes
author Melotti, Claudia Z
author_facet Melotti, Claudia Z
Amary, Maria Fernanda Carriel
Sotto, Miriam Nacagami
Diss, Timothy
Sanches, Jose Antonio
author_role author
author2 Amary, Maria Fernanda Carriel
Sotto, Miriam Nacagami
Diss, Timothy
Sanches, Jose Antonio
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Melotti, Claudia Z
Amary, Maria Fernanda Carriel
Sotto, Miriam Nacagami
Diss, Timothy
Sanches, Jose Antonio
dc.subject.por.fl_str_mv Cutaneous lymphoma
Polymerase chain reaction
Gene rearrangement
Clonality
B-cell
Lymphoproliferative processes
topic Cutaneous lymphoma
Polymerase chain reaction
Gene rearrangement
Clonality
B-cell
Lymphoproliferative processes
description INTRODUCTION: The differential diagnosis of B-cell lymphoproliferative processes remains a challenge for pathologists, dermatologists and oncologists, despite advances in histology, immunohistochemistry and molecular biology. OBJECTIVE: Evaluate aid and limitations of clonality analysis in the diagnosis of primary cutaneous B-cell lymphomas and B-cell pseudolymphomas. METHODS: This study included 29 cases of B-cell lymphoproliferative processes classified as primary cutaneous B-cell lymphomas (13), B-cell pseudolymphomas (6) and inconclusive cases (10) using histology and immunohistochemistry. The clonality analysis was performed by polymerase chain reaction analysis of immunoglobulin light chain and heavy chain rearrangements. RESULTS: DNA quality was shown to be generally poor; eight samples were inadequate for polymerase chain reaction analysis. The results showed monoclonality in eight of the primary cutaneous B-cell lymphomas and polyclonality in four of the B-cell pseudolymphomas. In addition, monoclonality was shown in two of the inconclusive cases by histology and immunohistochemistry, demonstrating the utility of polymerase chain reaction as an ancillary diagnostic tool for primary cutaneous B-cell lymphomas. DISCUSSION: The low quality DNA extracted from these cases demanded the use of an IgH protocol that yielded small fragments and IgK. Both methods used together improved detection. CONCLUSION: Use of the two protocols, immunoglobulin heavy chain FR3-trad and immunoglobulin light chain-Kappa Biomed protocols for clonality analysis improved diagnostic accuracy.
publishDate 2010
dc.date.none.fl_str_mv 2010-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/clinics/article/view/18422
10.1590/S1807-59322010000100009
url https://www.revistas.usp.br/clinics/article/view/18422
identifier_str_mv 10.1590/S1807-59322010000100009
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/clinics/article/view/18422/20485
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
publisher.none.fl_str_mv Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo
dc.source.none.fl_str_mv Clinics; Vol. 65 No. 1 (2010); 53-60
Clinics; v. 65 n. 1 (2010); 53-60
Clinics; Vol. 65 Núm. 1 (2010); 53-60
1980-5322
1807-5932
reponame:Clinics
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Clinics
collection Clinics
repository.name.fl_str_mv Clinics - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||clinics@hc.fm.usp.br
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