Hairy cell leukemia in older adult: Case report and literature review

Detalhes bibliográficos
Autor(a) principal: Lopez Muñoz, Diego Fernando
Data de Publicação: 2023
Outros Autores: Cabrera Bautista, Jackson Nikolai, Becerra Zuleta, Laura Daniela, Granada Ibanez, Juan Carlos, Londoño Llano, Valeria, Ocoro Gonzalez, Marling Xiomara, Rivera Villota, Juan Diego
Tipo de documento: Artigo
Idioma: spa
Título da fonte: Research, Society and Development
Texto Completo: https://rsdjournal.org/index.php/rsd/article/view/44355
Resumo: Hairy cell leukemia (HCL) is a very rare type of B-cell cancer characterized by the presence of hairy cells in peripheral blood and bone marrow. It mainly affects adult males with a median age of 50 years. Hairy cells are positive for tartrate-resistant acid phosphatase (TRAP) staining and express surface markers CD11c, CD20, CD22, CD25, and CD103. The identification of the BRAF V600E mutation in 2016 has provided a notable diagnostic tool, found in almost 80% of all HCL patients. Currently, the possibility of a multiparametric approach to diagnosis is opening up. Clinical case: A 78-year-old man presents symptoms of marked asthenia, adynamia, hyporexia, and unquantified weight loss, as well as a feeling of gastric fullness. Physical examination reveals a globular, distended abdomen and a palpable splenomegaly of 6 cm, without adenopathies or hepatomegaly. Controlled hypertensive history. He works in agricultural tasks and is frequently in contact with insecticides and pesticides. Conclusion: HCL commonly presents with pancytopenia, splenomegaly, and monocytopenia, characterized by the presence of medium-sized lymphoid cells with broad cytoplasm and cytoplasmic projections that give a hairy appearance in peripheral blood. Diagnosis is established through clinical symptoms, bone marrow aspiration and biopsy, flow cytometry, and other complementary tests.words: Leukemia, Hairy Cell, Flow Cytometry, Bone Marrow, Cell Cycle, Epigenomics.
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spelling Hairy cell leukemia in older adult: Case report and literature reviewLeucemia de células pilosas en adulto mayor: Reporte de caso y revisión de literaturaLeucemia de células pilosas em idosos: Relato de caso e revisão de literaturaLeucemia de células pilosasCitometria de fluxoPancitopeniaEsplenomegaliaProteínas proto-oncogênicas B-raf.Leucemia de células peludasCitometría de flujoPancitopeniaEsplenomegaliaProteínas proto-oncogénicas B-raf.Leukemia hairy cellFlow cytometryPancytopeniaSplenomegalyProteínas proto-oncogénicas B-raf. Hairy cell leukemia (HCL) is a very rare type of B-cell cancer characterized by the presence of hairy cells in peripheral blood and bone marrow. It mainly affects adult males with a median age of 50 years. Hairy cells are positive for tartrate-resistant acid phosphatase (TRAP) staining and express surface markers CD11c, CD20, CD22, CD25, and CD103. The identification of the BRAF V600E mutation in 2016 has provided a notable diagnostic tool, found in almost 80% of all HCL patients. Currently, the possibility of a multiparametric approach to diagnosis is opening up. Clinical case: A 78-year-old man presents symptoms of marked asthenia, adynamia, hyporexia, and unquantified weight loss, as well as a feeling of gastric fullness. Physical examination reveals a globular, distended abdomen and a palpable splenomegaly of 6 cm, without adenopathies or hepatomegaly. Controlled hypertensive history. He works in agricultural tasks and is frequently in contact with insecticides and pesticides. Conclusion: HCL commonly presents with pancytopenia, splenomegaly, and monocytopenia, characterized by the presence of medium-sized lymphoid cells with broad cytoplasm and cytoplasmic projections that give a hairy appearance in peripheral blood. Diagnosis is established through clinical symptoms, bone marrow aspiration and biopsy, flow cytometry, and other complementary tests.words: Leukemia, Hairy Cell, Flow Cytometry, Bone Marrow, Cell Cycle, Epigenomics.La leucemia de células pilosas (LCP) es un tipo de cáncer muy infrecuente de células B, caracterizado por la presencia de células vellosas en sangre periférica y médula ósea. Afecta principalmente a varones adultos con una mediana de edad de 50 años. Las células pilosas son positivas para la tinción fosfatasa ácida resistente a tartrato (FART) y expresan marcadores de superficie, CD11c, CD20, CD22, CD25 y CD103. La identificación de la mutación BRAF V600E en 2016 ha proporcionado una herramienta de diagnóstico notable, se encuentra en casi un 80% de todos los pacientes con LCP. Actualmente, se abre la posibilidad de un enfoque multiparamétrico para el diagnóstico. Caso clínico: hombre de 78 años, presenta síntomas de astenia marcada, adinamia, hiporexia y pérdida de peso no cuantificada, además de sensación de plenitud gástrica. Examen físico, se observa un abdomen globuloso, distendido y una esplenomegalia palpable de 6 cm, sin adenopatías ni hepatomegalia. Patológicos hipertensos controlado. Trabaja en labores agrícolas y está en contacto frecuente con insecticidas y pesticidas. Conclusión: LCP, se presenta comúnmente con pancitopenia, esplenomegalia y monocitopenia, se caracteriza por la presencia de células linfoides de tamaño mediano con citoplasma amplio y por tener prolongaciones citoplasmáticas que le dan un aspecto velloso en sangre periférica. El diagnóstico se establece mediante la sintomatología clínica, aspirado y biopsia de médula ósea, citometría de flujo y otras pruebas complementarias.Antecedentes: A leucemia de células pilosas (LCP) é um tipo muito raro de câncer de células B, caracterizado pela presença de células pilosas no sangue periférico e na medula óssea. Afeta principalmente homens adultos com uma idade média de 50 anos. As células ciliadas são positivas para a coloração fosfatase ácida resistente ao tartarato (FART) e expressam marcadores de superfície, CD11c, CD20, CD22, CD25 e CD103. A identificação da mutação BRAF V600E em 2016 forneceu uma ferramenta de diagnóstico notável, encontrada em quase 80% de todos os pacientes com LCP. Atualmente, abre-se a possibilidade de uma abordagem multiparamétrica para o diagnóstico. Caso clínico: homem de 78 anos, apresenta sintomas de astenia marcada, adinamia, hiporexia e perda de peso não quantificada, além de sensação de plenitude gástrica. Exame físico, observa-se abdome globuloso, distendido e esplenomegalia palpável de 6 cm, sem adenopatias ou hepatomegalia. Patológicos hipertensos controlados. Trabalha na agricultura e tem contato frequente com inseticidas e pesticidas. Conclusão: LCP, comumente apresentado com pancitopenia, esplenomegalia e monocitopenia, caracteriza-se pela presença de células linfóides de tamanho médio com citoplasma amplo e por ter prolongamentos citoplasmáticos que lhe dão aspecto peludo em sangue periférico. O diagnóstico é estabelecido por sintomatologia clínica, aspiração e biópsia da medula óssea, citometria de fluxo e outros exames complementares.Research, Society and Development2023-12-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://rsdjournal.org/index.php/rsd/article/view/4435510.33448/rsd-v12i13.44355Research, Society and Development; Vol. 12 No. 13; e117121344355Research, Society and Development; Vol. 12 Núm. 13; e117121344355Research, Society and Development; v. 12 n. 13; e1171213443552525-3409reponame:Research, Society and Developmentinstname:Universidade Federal de Itajubá (UNIFEI)instacron:UNIFEIspahttps://rsdjournal.org/index.php/rsd/article/view/44355/35522Copyright (c) 2023 Diego Fernando Lopez Muñoz; Jackson Nikolai Cabrera Bautista; Laura Daniela Becerra Zuleta; Juan Carlos Granada Ibanez; Valeria Londoño Llano; Marling Xiomara Ocoro Gonzalez; Juan Diego Rivera Villotahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessLopez Muñoz, Diego FernandoCabrera Bautista, Jackson NikolaiBecerra Zuleta, Laura Daniela Granada Ibanez, Juan Carlos Londoño Llano, ValeriaOcoro Gonzalez, Marling Xiomara Rivera Villota, Juan Diego2023-12-11T09:52:06Zoai:ojs.pkp.sfu.ca:article/44355Revistahttps://rsdjournal.org/index.php/rsd/indexPUBhttps://rsdjournal.org/index.php/rsd/oairsd.articles@gmail.com2525-34092525-3409opendoar:2023-12-11T09:52:06Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)false
dc.title.none.fl_str_mv Hairy cell leukemia in older adult: Case report and literature review
Leucemia de células pilosas en adulto mayor: Reporte de caso y revisión de literatura
Leucemia de células pilosas em idosos: Relato de caso e revisão de literatura
title Hairy cell leukemia in older adult: Case report and literature review
spellingShingle Hairy cell leukemia in older adult: Case report and literature review
Lopez Muñoz, Diego Fernando
Leucemia de células pilosas
Citometria de fluxo
Pancitopenia
Esplenomegalia
Proteínas proto-oncogênicas B-raf.
Leucemia de células peludas
Citometría de flujo
Pancitopenia
Esplenomegalia
Proteínas proto-oncogénicas B-raf.
Leukemia hairy cell
Flow cytometry
Pancytopenia
Splenomegaly
Proteínas proto-oncogénicas B-raf.
title_short Hairy cell leukemia in older adult: Case report and literature review
title_full Hairy cell leukemia in older adult: Case report and literature review
title_fullStr Hairy cell leukemia in older adult: Case report and literature review
title_full_unstemmed Hairy cell leukemia in older adult: Case report and literature review
title_sort Hairy cell leukemia in older adult: Case report and literature review
author Lopez Muñoz, Diego Fernando
author_facet Lopez Muñoz, Diego Fernando
Cabrera Bautista, Jackson Nikolai
Becerra Zuleta, Laura Daniela
Granada Ibanez, Juan Carlos
Londoño Llano, Valeria
Ocoro Gonzalez, Marling Xiomara
Rivera Villota, Juan Diego
author_role author
author2 Cabrera Bautista, Jackson Nikolai
Becerra Zuleta, Laura Daniela
Granada Ibanez, Juan Carlos
Londoño Llano, Valeria
Ocoro Gonzalez, Marling Xiomara
Rivera Villota, Juan Diego
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Lopez Muñoz, Diego Fernando
Cabrera Bautista, Jackson Nikolai
Becerra Zuleta, Laura Daniela
Granada Ibanez, Juan Carlos
Londoño Llano, Valeria
Ocoro Gonzalez, Marling Xiomara
Rivera Villota, Juan Diego
dc.subject.por.fl_str_mv Leucemia de células pilosas
Citometria de fluxo
Pancitopenia
Esplenomegalia
Proteínas proto-oncogênicas B-raf.
Leucemia de células peludas
Citometría de flujo
Pancitopenia
Esplenomegalia
Proteínas proto-oncogénicas B-raf.
Leukemia hairy cell
Flow cytometry
Pancytopenia
Splenomegaly
Proteínas proto-oncogénicas B-raf.
topic Leucemia de células pilosas
Citometria de fluxo
Pancitopenia
Esplenomegalia
Proteínas proto-oncogênicas B-raf.
Leucemia de células peludas
Citometría de flujo
Pancitopenia
Esplenomegalia
Proteínas proto-oncogénicas B-raf.
Leukemia hairy cell
Flow cytometry
Pancytopenia
Splenomegaly
Proteínas proto-oncogénicas B-raf.
description Hairy cell leukemia (HCL) is a very rare type of B-cell cancer characterized by the presence of hairy cells in peripheral blood and bone marrow. It mainly affects adult males with a median age of 50 years. Hairy cells are positive for tartrate-resistant acid phosphatase (TRAP) staining and express surface markers CD11c, CD20, CD22, CD25, and CD103. The identification of the BRAF V600E mutation in 2016 has provided a notable diagnostic tool, found in almost 80% of all HCL patients. Currently, the possibility of a multiparametric approach to diagnosis is opening up. Clinical case: A 78-year-old man presents symptoms of marked asthenia, adynamia, hyporexia, and unquantified weight loss, as well as a feeling of gastric fullness. Physical examination reveals a globular, distended abdomen and a palpable splenomegaly of 6 cm, without adenopathies or hepatomegaly. Controlled hypertensive history. He works in agricultural tasks and is frequently in contact with insecticides and pesticides. Conclusion: HCL commonly presents with pancytopenia, splenomegaly, and monocytopenia, characterized by the presence of medium-sized lymphoid cells with broad cytoplasm and cytoplasmic projections that give a hairy appearance in peripheral blood. Diagnosis is established through clinical symptoms, bone marrow aspiration and biopsy, flow cytometry, and other complementary tests.words: Leukemia, Hairy Cell, Flow Cytometry, Bone Marrow, Cell Cycle, Epigenomics.
publishDate 2023
dc.date.none.fl_str_mv 2023-12-07
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://rsdjournal.org/index.php/rsd/article/view/44355
10.33448/rsd-v12i13.44355
url https://rsdjournal.org/index.php/rsd/article/view/44355
identifier_str_mv 10.33448/rsd-v12i13.44355
dc.language.iso.fl_str_mv spa
language spa
dc.relation.none.fl_str_mv https://rsdjournal.org/index.php/rsd/article/view/44355/35522
dc.rights.driver.fl_str_mv https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Research, Society and Development
publisher.none.fl_str_mv Research, Society and Development
dc.source.none.fl_str_mv Research, Society and Development; Vol. 12 No. 13; e117121344355
Research, Society and Development; Vol. 12 Núm. 13; e117121344355
Research, Society and Development; v. 12 n. 13; e117121344355
2525-3409
reponame:Research, Society and Development
instname:Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
instname_str Universidade Federal de Itajubá (UNIFEI)
instacron_str UNIFEI
institution UNIFEI
reponame_str Research, Society and Development
collection Research, Society and Development
repository.name.fl_str_mv Research, Society and Development - Universidade Federal de Itajubá (UNIFEI)
repository.mail.fl_str_mv rsd.articles@gmail.com
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