Atypical Presentation of Acute Lymphoid Leukemia in Child: Case Report
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , |
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/190 |
Resumo: | Introduction: Acute lymphoblastic leukemia (ALL) is the most common malignant neoplasm in children and the leading cause of cancer death in this age group. Hypercalcemia associated with frank osteolytic lesions is a rare presentation of ALL. Case Report: 9-year-old male, 37 kg, presented with headache, pain and functional impotence in the lower right leg for 15 days. Laboratory tests showed elevation of erythrocyte sedimentation rate and C-reactive protein with hypercalcemia. Imaging studies revealed bone demineralization and diffuse osteolytic lesions. Bone marrow aspiration showed 10% of blasts, which did not characterize leukemia. Due to the improvement of his clinical condition, the patient continued the clinical investigation as an outpatient. Biopsy of lytic lesion in the hip and new bone marrow aspirations detected higher number of blasts and confirmed the diagnosis of ALL. Treatment was initiated, following the protocol of the Brazilian Group of Treatment of Leukemia in Childhood, 2009. After two years, he was well and without disease. Conclusion: Hypercalcemia is associated with only 0.6% to 4.8% of all ALL cases. The patient presented only diffuse bone pain and hypercalcemia, without the usual symptoms, which makes his clinical condition even rarer, with such presentation being very scarce in the literature. Although uncommon, hypercalcemia and diffuse osteolytic lesions may be the first and only manifestations of ALL in the pediatric range. The present report is important in helping to formulate early diagnosis of childhood leukemia, even in the presence of an atypical clinical condition. |
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Atypical Presentation of Acute Lymphoid Leukemia in Child: Case ReportPresettación Atípica de Leucemia Linfoide Aguda en Niño: Relato de CasoApresentação Atípica de Leucemia Linfoide Aguda em Criança: Relato de CasoLeucemia-Linfoma Linfoblástico de Células PrecursorasHipercalcemiaDiagnóstico PrecoceCriançaPrecursor Cell Lymphoblastic Leukemia-LymphomaHypercalcemiaEarly DiagnosisChildLeucemia-Linfoma Linfoblástico de Células PrecursorasHipercalcemiaDiagnóstico PrecozNiñoIntroduction: Acute lymphoblastic leukemia (ALL) is the most common malignant neoplasm in children and the leading cause of cancer death in this age group. Hypercalcemia associated with frank osteolytic lesions is a rare presentation of ALL. Case Report: 9-year-old male, 37 kg, presented with headache, pain and functional impotence in the lower right leg for 15 days. Laboratory tests showed elevation of erythrocyte sedimentation rate and C-reactive protein with hypercalcemia. Imaging studies revealed bone demineralization and diffuse osteolytic lesions. Bone marrow aspiration showed 10% of blasts, which did not characterize leukemia. Due to the improvement of his clinical condition, the patient continued the clinical investigation as an outpatient. Biopsy of lytic lesion in the hip and new bone marrow aspirations detected higher number of blasts and confirmed the diagnosis of ALL. Treatment was initiated, following the protocol of the Brazilian Group of Treatment of Leukemia in Childhood, 2009. After two years, he was well and without disease. Conclusion: Hypercalcemia is associated with only 0.6% to 4.8% of all ALL cases. The patient presented only diffuse bone pain and hypercalcemia, without the usual symptoms, which makes his clinical condition even rarer, with such presentation being very scarce in the literature. Although uncommon, hypercalcemia and diffuse osteolytic lesions may be the first and only manifestations of ALL in the pediatric range. The present report is important in helping to formulate early diagnosis of childhood leukemia, even in the presence of an atypical clinical condition.Introducción: La leucemia linfoblástica aguda (LLA) es la neoplasia maligna más común en los niños y principal causa de muerte por cáncer en ese grupo de edad. La hipercalcemia asociada a lesiones osteolíticas francas es una rara presentación de LLA. Relato del Caso: Paciente de 9 años, masculino, 37kg, presentaba cefalea, dolor e impotencia funcional en miembro inferior derecho hace 15 días. Los exámenes de laboratorio evidenciaron elevación de velocidad de sedimentación globular y proteína C reactiva con hipercalcemia. En los exámenes de imagen, presentaba desmineralización ósea y lesiones osteolíticas difusas. Aspirado de médula ósea (MO) evidenció el 10% de blastos, lo que no caracterizó la leucemia. Debido a la mejora del cuadro clínico, el paciente siguió la investigación diagnóstica ambulatoriamente. La biopsia de lesión lítica en cadera y nuevo aspirado de MO detectaron mayor número de blastos y confirmaron el diagnóstico de LLA. Se inició tratamiento con protocolo del Grupo Brasileño de Tratamiento de Leucemias en la Infancia, 2009. Conclusión: La hipercalcemia está asociada a sólo 0,6% a 4,8% de los casos de LLA. El paciente en cuestión presentaba sólo dolores óseos difusas e hipercalcemia, sin la sintomatología habitual, lo que hace el cuadro clínico del paciente aún más raro, siendo tal presentación muy escasa en la literatura. A pesar de inusual, hipercalcemia y lesiones osteolíticas difusas pueden ser las primeras y únicas manifestaciones de LLA en niños. El presente relato se vuelve importante al ayudar a la formulación de diagnósticos precoces de la leucemia infantil, incluso en la vigencia de un cuadro clínico atípico.Introdução: A leucemia linfoblástica aguda (LLA) é a neoplasia maligna mais comum em crianças e a principal causa de morte por câncer nessa faixa etária. A hipercalcemia associada a lesões osteolíticas francas é uma rara apresentação da LLA. Relato do Caso: Paciente de 9 anos, sexo masculino, 37kg, apresentava cefaleia, dor e impotência funcional em membro inferior direito há 15 dias. Exames laboratoriais evidenciaram elevação de velocidade de hemossedimentação e proteína C reativa com hipercalcemia. Nos exames de imagem, apresentava desmineralização óssea e lesões osteolíticas difusas. Aspirado de medula óssea (MO) evidenciou 10% de blastos, o que não caracterizou leucemia. Pela melhora do quadro clínico, o paciente seguiu com investigação diagnóstica ambulatorialmente. Biópsia de lesão lítica em quadril e novo aspirado de MO detectaram maior número de blastos e confirmaram o diagnóstico de LLA. Iniciou tratamento com protocolo do Grupo Brasileiro de Tratamento de Leucemias na Infância, 2009. Após dois anos, estava bem e sem doença. Conclusão: A hipercalcemia está associada a apenas 0,6% a 4,8% dos casos de LLA. O paciente em questão apresentava apenas dores ósseas difusas e hipercalcemia, sem a sintomatologia habitual, o que torna seu quadro clínico ainda mais raro, sendo tal apresentação muito escassa na literatura. Apesar de incomuns, hipercalcemia e lesões osteolíticas difusas podem ser as primeiras e únicas manifestações de LLA na faixa pediátrica. O presente relato torna-se importante ao auxiliar a formulação de diagnósticos precoces da leucemia infantil, mesmo na vigência de um quadro clínico atípico.INCA2019-12-16info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionRelato de Casoapplication/pdfapplication/pdfhttps://rbc.inca.gov.br/index.php/revista/article/view/19010.32635/2176-9745.RBC.2019v65n4.190Revista Brasileira de Cancerologia; Vol. 65 No. 4 (2019): Oct./Nov./Dec.; e-02190Revista Brasileira de Cancerologia; Vol. 65 Núm. 4 (2019): oct./nov./dic.; e-02190Revista Brasileira de Cancerologia; v. 65 n. 4 (2019): out./nov./dez.; e-021902176-9745reponame: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/190/497https://rbc.inca.gov.br/index.php/revista/article/view/190/641Copyright (c) 2019 Revista Brasileira de Cancerologiainfo:eu-repo/semantics/openAccessBasso Dias, PaulaLopes Luiz, Ana PaulaCosta Lima Lichtvan, LenizaGarcia de Lima, Adriano Luis2021-11-29T20:03:30Zoai:rbc.inca.gov.br:article/190Revistahttps://rbc.inca.gov.br/index.php/revistaPUBhttps://rbc.inca.gov.br/index.php/revista/oairbc@inca.gov.br0034-71162176-9745opendoar:2021-11-29T20:03:30Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)false |
dc.title.none.fl_str_mv |
Atypical Presentation of Acute Lymphoid Leukemia in Child: Case Report Presettación Atípica de Leucemia Linfoide Aguda en Niño: Relato de Caso Apresentação Atípica de Leucemia Linfoide Aguda em Criança: Relato de Caso |
title |
Atypical Presentation of Acute Lymphoid Leukemia in Child: Case Report |
spellingShingle |
Atypical Presentation of Acute Lymphoid Leukemia in Child: Case Report Basso Dias, Paula Leucemia-Linfoma Linfoblástico de Células Precursoras Hipercalcemia Diagnóstico Precoce Criança Precursor Cell Lymphoblastic Leukemia-Lymphoma Hypercalcemia Early Diagnosis Child Leucemia-Linfoma Linfoblástico de Células Precursoras Hipercalcemia Diagnóstico Precoz Niño |
title_short |
Atypical Presentation of Acute Lymphoid Leukemia in Child: Case Report |
title_full |
Atypical Presentation of Acute Lymphoid Leukemia in Child: Case Report |
title_fullStr |
Atypical Presentation of Acute Lymphoid Leukemia in Child: Case Report |
title_full_unstemmed |
Atypical Presentation of Acute Lymphoid Leukemia in Child: Case Report |
title_sort |
Atypical Presentation of Acute Lymphoid Leukemia in Child: Case Report |
author |
Basso Dias, Paula |
author_facet |
Basso Dias, Paula Lopes Luiz, Ana Paula Costa Lima Lichtvan, Leniza Garcia de Lima, Adriano Luis |
author_role |
author |
author2 |
Lopes Luiz, Ana Paula Costa Lima Lichtvan, Leniza Garcia de Lima, Adriano Luis |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Basso Dias, Paula Lopes Luiz, Ana Paula Costa Lima Lichtvan, Leniza Garcia de Lima, Adriano Luis |
dc.subject.por.fl_str_mv |
Leucemia-Linfoma Linfoblástico de Células Precursoras Hipercalcemia Diagnóstico Precoce Criança Precursor Cell Lymphoblastic Leukemia-Lymphoma Hypercalcemia Early Diagnosis Child Leucemia-Linfoma Linfoblástico de Células Precursoras Hipercalcemia Diagnóstico Precoz Niño |
topic |
Leucemia-Linfoma Linfoblástico de Células Precursoras Hipercalcemia Diagnóstico Precoce Criança Precursor Cell Lymphoblastic Leukemia-Lymphoma Hypercalcemia Early Diagnosis Child Leucemia-Linfoma Linfoblástico de Células Precursoras Hipercalcemia Diagnóstico Precoz Niño |
description |
Introduction: Acute lymphoblastic leukemia (ALL) is the most common malignant neoplasm in children and the leading cause of cancer death in this age group. Hypercalcemia associated with frank osteolytic lesions is a rare presentation of ALL. Case Report: 9-year-old male, 37 kg, presented with headache, pain and functional impotence in the lower right leg for 15 days. Laboratory tests showed elevation of erythrocyte sedimentation rate and C-reactive protein with hypercalcemia. Imaging studies revealed bone demineralization and diffuse osteolytic lesions. Bone marrow aspiration showed 10% of blasts, which did not characterize leukemia. Due to the improvement of his clinical condition, the patient continued the clinical investigation as an outpatient. Biopsy of lytic lesion in the hip and new bone marrow aspirations detected higher number of blasts and confirmed the diagnosis of ALL. Treatment was initiated, following the protocol of the Brazilian Group of Treatment of Leukemia in Childhood, 2009. After two years, he was well and without disease. Conclusion: Hypercalcemia is associated with only 0.6% to 4.8% of all ALL cases. The patient presented only diffuse bone pain and hypercalcemia, without the usual symptoms, which makes his clinical condition even rarer, with such presentation being very scarce in the literature. Although uncommon, hypercalcemia and diffuse osteolytic lesions may be the first and only manifestations of ALL in the pediatric range. The present report is important in helping to formulate early diagnosis of childhood leukemia, even in the presence of an atypical clinical condition. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-12-16 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Relato de Caso |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://rbc.inca.gov.br/index.php/revista/article/view/190 10.32635/2176-9745.RBC.2019v65n4.190 |
url |
https://rbc.inca.gov.br/index.php/revista/article/view/190 |
identifier_str_mv |
10.32635/2176-9745.RBC.2019v65n4.190 |
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/190/497 https://rbc.inca.gov.br/index.php/revista/article/view/190/641 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2019 Revista Brasileira de Cancerologia info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2019 Revista Brasileira de Cancerologia |
eu_rights_str_mv |
openAccess |
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application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
INCA |
publisher.none.fl_str_mv |
INCA |
dc.source.none.fl_str_mv |
Revista Brasileira de Cancerologia; Vol. 65 No. 4 (2019): Oct./Nov./Dec.; e-02190 Revista Brasileira de Cancerologia; Vol. 65 Núm. 4 (2019): oct./nov./dic.; e-02190 Revista Brasileira de Cancerologia; v. 65 n. 4 (2019): out./nov./dez.; e-02190 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) |
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rbc@inca.gov.br |
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