Hairy cell leukemia in older adult: Case report and literature review
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , |
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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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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1797052635279261696 |