Cutaneous Granulocytic Sarcoma Concomitant to the Diagnosis of Acute Promyelocytic Leukemia

Detalhes bibliográficos
Autor(a) principal: Feijó, Carolina Moreira
Data de Publicação: 2022
Outros Autores: Lopes, Germison Silva
Tipo de documento: Artigo
Idioma: por
eng
Título da fonte: Revista Brasileira de Cancerologia (Online)
Texto Completo: https://rbc.inca.gov.br/index.php/revista/article/view/2703
Resumo: Introduction: Granulocytic sarcoma (GS) is a rare extramedullary tumor, made up by immature myeloid cells. It occurs in 2% to 14% of patients with acute myeloid leukemia (AML). The association with promyelocytic leukemia (APL) is even more rare, especially as manifestation at the time of diagnosis. The present study exposes the case of a patient with cutaneous GS concomitant with a diagnosis of APL. Case report: Male patient, 30 years old, referred to the Hematology Department due to fever, odynophagia, intense adynamia, hyporexia, loss of 5 kg, night sweating, in addition to progressive dyspnea over one month. Laboratory exams were run with evidence of severe anemia, proceeding to etiological investigation with myelogram, which showed 84% of blasts, and immunophenotyping compatible with promyelocytic leukemia (APL), PML-RARA positive (90%). Also, presented ulcerated lesions in the genital region and right leg, whose biopsy showed proliferation of suspected round cells for infiltration by AML/GS. Immunohistochemistry confirmed GS. The patient underwent chemotherapy, with good response to the treatment and improvement of blood counts. Skin lesions evolved with healing. After the 3rd consolidation, PML-RARA was negative. Conclusion: This case report describes a rare presentation of a malignant hematological disease, GS, also known as skin chloroma. A diagnostic strategy including images, histopathology, immunohistochemistry and laboratory tests were needed for confirmation. Timely diagnosis is essential, so that appropriate treatment is instituted soon, benefiting the patient regarding survival and quality of life.
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spelling Cutaneous Granulocytic Sarcoma Concomitant to the Diagnosis of Acute Promyelocytic LeukemiaSarcoma Granulocitico Cutaneo de Presentacion Concomitente al Diagnostico de Leucemia Promielocitica AgudaSarcoma Granulocítico Cutâneo de Apresentação Concomitante ao Diagnóstico de Leucemia Promielocítica Agudasarcoma mieloideleucemia mieloide agudaleucemia promielocítica agudaneoplasias cutâneassarcoma, myeloidleukemia, myeloid, acuteleukemia, promyelocytic, acuteskin neoplasmssarcoma mieloideleucemia mieloide agudaleucemia promielocítica agudaneoplasias cutáneasIntroduction: Granulocytic sarcoma (GS) is a rare extramedullary tumor, made up by immature myeloid cells. It occurs in 2% to 14% of patients with acute myeloid leukemia (AML). The association with promyelocytic leukemia (APL) is even more rare, especially as manifestation at the time of diagnosis. The present study exposes the case of a patient with cutaneous GS concomitant with a diagnosis of APL. Case report: Male patient, 30 years old, referred to the Hematology Department due to fever, odynophagia, intense adynamia, hyporexia, loss of 5 kg, night sweating, in addition to progressive dyspnea over one month. Laboratory exams were run with evidence of severe anemia, proceeding to etiological investigation with myelogram, which showed 84% of blasts, and immunophenotyping compatible with promyelocytic leukemia (APL), PML-RARA positive (90%). Also, presented ulcerated lesions in the genital region and right leg, whose biopsy showed proliferation of suspected round cells for infiltration by AML/GS. Immunohistochemistry confirmed GS. The patient underwent chemotherapy, with good response to the treatment and improvement of blood counts. Skin lesions evolved with healing. After the 3rd consolidation, PML-RARA was negative. Conclusion: This case report describes a rare presentation of a malignant hematological disease, GS, also known as skin chloroma. A diagnostic strategy including images, histopathology, immunohistochemistry and laboratory tests were needed for confirmation. Timely diagnosis is essential, so that appropriate treatment is instituted soon, benefiting the patient regarding survival and quality of life.Introducción: El sarcoma granulocítico (SG) es un tumor extramedular poco frecuente, compuesto por células mieloides inmaduras. Ocurre en 2% a 14% de los pacientes con leucemia mieloide aguda (AML). La asociación con leucemia promielocítica (LPA) es aún más rara, especialmente como manifestación en el momento del diagnóstico. El presente estudio expone el caso de un paciente con SG cutáneo que presenta un diagnóstico de LPA. Relato del caso: Paciente masculino de 30 años, remitido al Servicio de Hematología por fiebre, odinofagia, adinamia intensa, hiporexia, pérdida de 5 kg, sudoración nocturna, además de disnea progresiva a lo largo de un mes. Realizó exámenes de laboratorio con evidencia de anemia severa, continuando investigación etiológica con mielograma, que mostró 84% de blastos, e inmunofenotipificación compatible con LPA, PML-RARA positivo (90%). También presentaba lesiones ulceradas en región genital y muslo derecho, en las que la biopsia mostró proliferación de células redondas sospechadas para infiltración por LMA/SG. La inmunohistoquímica confirmó SG. El paciente fue sometido a quimioterapia, con buena respuesta al tratamiento y mejoría de los hemogramas. Las lesiones cutáneas evolucionaron con la curación. Después de la tercera consolidación, el PML-RARA fue negativo. Conclusión: Este reporte de caso describe una presentación poco común de una enfermedad hematológica maligna, el SG, también conocido como cloroma, en la piel. Se necesitaba una estrategia de diagnóstico que incluyera imágenes, histopatología, inmunohistoquímica y pruebas de laboratorio para confirmarlo. El diagnóstico oportuno es fundamental para que pronto se instaure el tratamiento adecuado, beneficiando al paciente en cuanto a supervivencia y calidad de vida.Introdução: O sarcoma granulocítico (SG) é um tumor extramedular raro, composto por células mieloides imaturas. Ocorre em 2% a 14% dos pacientes com leucemia mieloide aguda (LMA). A associação com leucemia promielocítica (LPA) é ainda mais rara, especialmente como manifestação no momento do diagnóstico. O presente estudo expõe o caso de um paciente com SG cutâneo de apresentação concomitante ao diagnóstico de LPA. Relato do caso: Paciente do sexo masculino, 30 anos, encaminhado ao Departamento de Hematologia por febre, odinofagia, intensa adinamia, hiporexia, perda de 5 kg, sudorese noturna, além de dispneia progressiva ao longo de um mês. Realizou exames laboratoriais com evidência de anemia grave, prosseguindo investigação etiológica com mielograma, que evidenciou 84% de blastos, e imunofenotipagem compatível com LPA, PML-RARA positivo (90%). Apresentava ainda lesões ulceradas em região genital e coxa direita, cuja biópsia evidenciou proliferação de células redondas suspeita para infiltração por LMA/SG. A imuno-histoquímica confirmou SG. O paciente foi submetido à quimioterapia, com boa resposta ao tratamento e melhora das contagens sanguíneas. As lesões cutâneas evoluíram com cicatrização. Após terceira consolidação, o PML-RARA negativou. Conclusão: Este relato de caso descreve uma apresentação rara de uma doença hematológica maligna, o SG, também conhecido como cloroma, na pele. Uma estratégia de diagnóstico incluindo imagens, histopatologia, imuno-histoquímica e exames laboratoriais foi necessária para confirmá-lo. O diagnóstico oportuno é essencial para que o tratamento adequado seja instituído logo, beneficiando o paciente em sobrevida e qualidade de vida.INCA2022-10-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionRelato de Casoapplication/pdfapplication/pdftext/htmlhttps://rbc.inca.gov.br/index.php/revista/article/view/270310.32635/2176-9745.RBC.2022v68n4.2703Revista Brasileira de Cancerologia; Vol. 68 No. 4 (2022): Oct./Nov./Dec.; e-122703Revista Brasileira de Cancerologia; Vol. 68 Núm. 4 (2022): oct./nov./dic.; e-122703Revista Brasileira de Cancerologia; v. 68 n. 4 (2022): out./nov./dez.; e-1227032176-9745reponame:Revista Brasileira de Cancerologia (Online)instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)instacron:INCAporenghttps://rbc.inca.gov.br/index.php/revista/article/view/2703/2271https://rbc.inca.gov.br/index.php/revista/article/view/2703/2940https://rbc.inca.gov.br/index.php/revista/article/view/2703/2458Copyright (c) 2022 Revista Brasileira de Cancerologiahttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessFeijó, Carolina MoreiraLopes, Germison Silva2023-06-13T15:08:06Zoai:rbc.inca.gov.br:article/2703Revistahttps://rbc.inca.gov.br/index.php/revistaPUBhttps://rbc.inca.gov.br/index.php/revista/oairbc@inca.gov.br0034-71162176-9745opendoar:2023-06-13T15:08:06Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)false
dc.title.none.fl_str_mv Cutaneous Granulocytic Sarcoma Concomitant to the Diagnosis of Acute Promyelocytic Leukemia
Sarcoma Granulocitico Cutaneo de Presentacion Concomitente al Diagnostico de Leucemia Promielocitica Aguda
Sarcoma Granulocítico Cutâneo de Apresentação Concomitante ao Diagnóstico de Leucemia Promielocítica Aguda
title Cutaneous Granulocytic Sarcoma Concomitant to the Diagnosis of Acute Promyelocytic Leukemia
spellingShingle Cutaneous Granulocytic Sarcoma Concomitant to the Diagnosis of Acute Promyelocytic Leukemia
Feijó, Carolina Moreira
sarcoma mieloide
leucemia mieloide aguda
leucemia promielocítica aguda
neoplasias cutâneas
sarcoma, myeloid
leukemia, myeloid, acute
leukemia, promyelocytic, acute
skin neoplasms
sarcoma mieloide
leucemia mieloide aguda
leucemia promielocítica aguda
neoplasias cutáneas
title_short Cutaneous Granulocytic Sarcoma Concomitant to the Diagnosis of Acute Promyelocytic Leukemia
title_full Cutaneous Granulocytic Sarcoma Concomitant to the Diagnosis of Acute Promyelocytic Leukemia
title_fullStr Cutaneous Granulocytic Sarcoma Concomitant to the Diagnosis of Acute Promyelocytic Leukemia
title_full_unstemmed Cutaneous Granulocytic Sarcoma Concomitant to the Diagnosis of Acute Promyelocytic Leukemia
title_sort Cutaneous Granulocytic Sarcoma Concomitant to the Diagnosis of Acute Promyelocytic Leukemia
author Feijó, Carolina Moreira
author_facet Feijó, Carolina Moreira
Lopes, Germison Silva
author_role author
author2 Lopes, Germison Silva
author2_role author
dc.contributor.author.fl_str_mv Feijó, Carolina Moreira
Lopes, Germison Silva
dc.subject.por.fl_str_mv sarcoma mieloide
leucemia mieloide aguda
leucemia promielocítica aguda
neoplasias cutâneas
sarcoma, myeloid
leukemia, myeloid, acute
leukemia, promyelocytic, acute
skin neoplasms
sarcoma mieloide
leucemia mieloide aguda
leucemia promielocítica aguda
neoplasias cutáneas
topic sarcoma mieloide
leucemia mieloide aguda
leucemia promielocítica aguda
neoplasias cutâneas
sarcoma, myeloid
leukemia, myeloid, acute
leukemia, promyelocytic, acute
skin neoplasms
sarcoma mieloide
leucemia mieloide aguda
leucemia promielocítica aguda
neoplasias cutáneas
description Introduction: Granulocytic sarcoma (GS) is a rare extramedullary tumor, made up by immature myeloid cells. It occurs in 2% to 14% of patients with acute myeloid leukemia (AML). The association with promyelocytic leukemia (APL) is even more rare, especially as manifestation at the time of diagnosis. The present study exposes the case of a patient with cutaneous GS concomitant with a diagnosis of APL. Case report: Male patient, 30 years old, referred to the Hematology Department due to fever, odynophagia, intense adynamia, hyporexia, loss of 5 kg, night sweating, in addition to progressive dyspnea over one month. Laboratory exams were run with evidence of severe anemia, proceeding to etiological investigation with myelogram, which showed 84% of blasts, and immunophenotyping compatible with promyelocytic leukemia (APL), PML-RARA positive (90%). Also, presented ulcerated lesions in the genital region and right leg, whose biopsy showed proliferation of suspected round cells for infiltration by AML/GS. Immunohistochemistry confirmed GS. The patient underwent chemotherapy, with good response to the treatment and improvement of blood counts. Skin lesions evolved with healing. After the 3rd consolidation, PML-RARA was negative. Conclusion: This case report describes a rare presentation of a malignant hematological disease, GS, also known as skin chloroma. A diagnostic strategy including images, histopathology, immunohistochemistry and laboratory tests were needed for confirmation. Timely diagnosis is essential, so that appropriate treatment is instituted soon, benefiting the patient regarding survival and quality of life.
publishDate 2022
dc.date.none.fl_str_mv 2022-10-07
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv https://rbc.inca.gov.br/index.php/revista/article/view/2703
10.32635/2176-9745.RBC.2022v68n4.2703
url https://rbc.inca.gov.br/index.php/revista/article/view/2703
identifier_str_mv 10.32635/2176-9745.RBC.2022v68n4.2703
dc.language.iso.fl_str_mv por
eng
language por
eng
dc.relation.none.fl_str_mv https://rbc.inca.gov.br/index.php/revista/article/view/2703/2271
https://rbc.inca.gov.br/index.php/revista/article/view/2703/2940
https://rbc.inca.gov.br/index.php/revista/article/view/2703/2458
dc.rights.driver.fl_str_mv Copyright (c) 2022 Revista Brasileira de Cancerologia
https://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2022 Revista Brasileira de Cancerologia
https://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
text/html
dc.publisher.none.fl_str_mv INCA
publisher.none.fl_str_mv INCA
dc.source.none.fl_str_mv Revista Brasileira de Cancerologia; Vol. 68 No. 4 (2022): Oct./Nov./Dec.; e-122703
Revista Brasileira de Cancerologia; Vol. 68 Núm. 4 (2022): oct./nov./dic.; e-122703
Revista Brasileira de Cancerologia; v. 68 n. 4 (2022): out./nov./dez.; e-122703
2176-9745
reponame:Revista Brasileira de Cancerologia (Online)
instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
instacron:INCA
instname_str Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
instacron_str INCA
institution INCA
reponame_str Revista Brasileira de Cancerologia (Online)
collection Revista Brasileira de Cancerologia (Online)
repository.name.fl_str_mv Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)
repository.mail.fl_str_mv rbc@inca.gov.br
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