Signs and symptoms of rheumatic diseases as first manifestation of pediatric cancer: diagnosis and prognosis implications
To assess the prevalence and describe the clinical, laboratory and radiological findings, treatment and outcome of children with cancer initially referred to a tertiary outpatient pediatric rheumatology clinic. Retrospective analysis of medical records from patients identified in a list of 250 new p...
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creator | Fonseca, Mariana Bertoldi Gomes, Francisco Hugo Rodrigues Valera, Elvis Terci Pileggi, Gecilmara Salviato Gonfiantini, Paula Braga Gonfiantini, Marcela Braga Ferriani, Virgínia Paes Leme Carvalho, Luciana Martins de |
description | To assess the prevalence and describe the clinical, laboratory and radiological findings, treatment and outcome of children with cancer initially referred to a tertiary outpatient pediatric rheumatology clinic.
Retrospective analysis of medical records from patients identified in a list of 250 new patients attending the tertiary Pediatric Rheumatology Clinic, Ribeirão Preto Medical School hospital, University of São Paulo, from July 2013 to July 2015, whose final diagnosis was cancer.
Of 250 patients seen during the study period, 5 (2%) had a cancer diagnosis. Among them, 80% had constitutional symptoms, especially weight loss and asthenia, and 60% had arthritis. Initially, all patients had at least one alteration in their blood count, lactate dehydrogenase was increased in 80% and a bone marrow smear was conclusive in 60% of patients. Bone and intestine biopsies were necessary for the diagnosis in 2 patients. JIA was the most common initial diagnosis. The definitive diagnosis was acute lymphoblastic leukemia (2 patients), M3 acute myeloid leukemia, lymphoma, and neuroblastoma (one case each). Of 5 patients studied, 3 (60%) are in remission and 2 (40%) died, one of them with prior use of steroids.
The constitutional and musculoskeletal symptoms common to rheumatic and neoplastic diseases can delay the diagnosis and consequently worsen the prognosis of neoplasms. Initial blood count and bone marrow smear may be normal in the initial framework of neoplasms. Thus, the clinical follow-up of these cases becomes imperative and the treatment, mainly with corticosteroids, should be delayed until diagnostic definition.
Avaliar a prevalência e descrever as principais manifestações clínicas, exames complementares, tratamento e evolução de crianças com doenças neoplásicas atendidas inicialmente em um serviço terciário de reumatologia pediátrica.
Analisamos retrospectivamente o prontuário médico de pacientes com diagnóstico definitivo de neoplasia, identificados entre 250 casos novos atendidos no ambulatório de reumatologia pediátrica do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto-USP, no período de julho de 2013 a julho de 2015.
Dos 250 pacientes recebidos pelo ambulatório no período do estudo, 5 (2%) tiveram diagnóstico de neoplasia. Desses 5 pacientes, 80% apresentavam sintomas constitucionais, principalmente perda de peso e astenia e 60% artrite. Inicialmente, todos apresentavam pelo menos uma série alterada no hemograma, 80% aumento da desidro |
doi_str_mv | 10.1016/j.rbre.2017.01.007 |
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Retrospective analysis of medical records from patients identified in a list of 250 new patients attending the tertiary Pediatric Rheumatology Clinic, Ribeirão Preto Medical School hospital, University of São Paulo, from July 2013 to July 2015, whose final diagnosis was cancer.
Of 250 patients seen during the study period, 5 (2%) had a cancer diagnosis. Among them, 80% had constitutional symptoms, especially weight loss and asthenia, and 60% had arthritis. Initially, all patients had at least one alteration in their blood count, lactate dehydrogenase was increased in 80% and a bone marrow smear was conclusive in 60% of patients. Bone and intestine biopsies were necessary for the diagnosis in 2 patients. JIA was the most common initial diagnosis. The definitive diagnosis was acute lymphoblastic leukemia (2 patients), M3 acute myeloid leukemia, lymphoma, and neuroblastoma (one case each). Of 5 patients studied, 3 (60%) are in remission and 2 (40%) died, one of them with prior use of steroids.
The constitutional and musculoskeletal symptoms common to rheumatic and neoplastic diseases can delay the diagnosis and consequently worsen the prognosis of neoplasms. Initial blood count and bone marrow smear may be normal in the initial framework of neoplasms. Thus, the clinical follow-up of these cases becomes imperative and the treatment, mainly with corticosteroids, should be delayed until diagnostic definition.
Avaliar a prevalência e descrever as principais manifestações clínicas, exames complementares, tratamento e evolução de crianças com doenças neoplásicas atendidas inicialmente em um serviço terciário de reumatologia pediátrica.
Analisamos retrospectivamente o prontuário médico de pacientes com diagnóstico definitivo de neoplasia, identificados entre 250 casos novos atendidos no ambulatório de reumatologia pediátrica do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto-USP, no período de julho de 2013 a julho de 2015.
Dos 250 pacientes recebidos pelo ambulatório no período do estudo, 5 (2%) tiveram diagnóstico de neoplasia. Desses 5 pacientes, 80% apresentavam sintomas constitucionais, principalmente perda de peso e astenia e 60% artrite. Inicialmente, todos apresentavam pelo menos uma série alterada no hemograma, 80% aumento da desidrogenase lática (LDH) e 60% mielograma confirmatório. Dois pacientes necessitaram de biópsia, óssea e intestino, para o diagnóstico final. Artrite idiopática juvenil foi o diagnóstico inicial mais frequente. Os diagnósticos definitivos foram leucemia linfóide aguda (2 casos), leucemia mielóide aguda-M3, neuroblastoma e linfoma (1 caso cada). Dos pacientes estudados 3 (60%) estão em remissão. Dois pacientes foram a óbito (40%), um deles com uso prévio de corticoide.
Os sintomas constitucionais e musculoesqueléticos comuns às doenças reumáticas e neoplásicas podem retardar o diagnóstico e consequentemente agravar o prognóstico das neoplasias. O hemograma inicial, assim como o mielograma, podem estar normais no quadro inicial das neoplasias. Dessa forma, o seguimento clínico evolutivo destes casos torna-se imperativo e o tratamento, principalmente com corticoides, deve ser retardado até definição diagnóstica.</description><identifier>ISSN: 2255-5021</identifier><identifier>ISSN: 1809-4570</identifier><identifier>EISSN: 2255-5021</identifier><identifier>DOI: 10.1016/j.rbre.2017.01.007</identifier><identifier>PMID: 28743360</identifier><language>eng</language><publisher>Brazil: Elsevier Editora Ltda</publisher><subject>Arthralgia - etiology ; Artrite idiopática juvenil ; Asthenia - etiology ; Child ; Child, Preschool ; Diagnosis, Differential ; Doenças reumáticas, Pediatria ; Female ; Humans ; Juvenile idiopathic arthritis ; Male ; Musculoskeletal symptoms ; Neoplasia ; Neoplasms - diagnosis ; Neoplasms - physiopathology ; Neoplastic diseases ; Pediatric rheumatic disease ; Retrospective Studies ; Rheumatic Diseases - diagnosis ; Rheumatic Diseases - physiopathology ; Sintomas musculoesqueléticos</subject><ispartof>Revista Brasileira de Reumatologia, 2017-07, Vol.57 (4), p.330-337</ispartof><rights>2017 Elsevier Editora Ltda.</rights><rights>Copyright © 2017 Elsevier Editora Ltda. All rights reserved.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3507-10847ae0816dcaacc54d2f6ecd5a258599a7634037ca6e7e7ad9f7db632d5cf43</citedby><cites>FETCH-LOGICAL-c3507-10847ae0816dcaacc54d2f6ecd5a258599a7634037ca6e7e7ad9f7db632d5cf43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28743360$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fonseca, Mariana Bertoldi</creatorcontrib><creatorcontrib>Gomes, Francisco Hugo Rodrigues</creatorcontrib><creatorcontrib>Valera, Elvis Terci</creatorcontrib><creatorcontrib>Pileggi, Gecilmara Salviato</creatorcontrib><creatorcontrib>Gonfiantini, Paula Braga</creatorcontrib><creatorcontrib>Gonfiantini, Marcela Braga</creatorcontrib><creatorcontrib>Ferriani, Virgínia Paes Leme</creatorcontrib><creatorcontrib>Carvalho, Luciana Martins de</creatorcontrib><title>Signs and symptoms of rheumatic diseases as first manifestation of pediatric cancer: diagnosis and prognosis implications</title><title>Revista Brasileira de Reumatologia</title><addtitle>Rev Bras Reumatol Engl Ed</addtitle><description>To assess the prevalence and describe the clinical, laboratory and radiological findings, treatment and outcome of children with cancer initially referred to a tertiary outpatient pediatric rheumatology clinic.
Retrospective analysis of medical records from patients identified in a list of 250 new patients attending the tertiary Pediatric Rheumatology Clinic, Ribeirão Preto Medical School hospital, University of São Paulo, from July 2013 to July 2015, whose final diagnosis was cancer.
Of 250 patients seen during the study period, 5 (2%) had a cancer diagnosis. Among them, 80% had constitutional symptoms, especially weight loss and asthenia, and 60% had arthritis. Initially, all patients had at least one alteration in their blood count, lactate dehydrogenase was increased in 80% and a bone marrow smear was conclusive in 60% of patients. Bone and intestine biopsies were necessary for the diagnosis in 2 patients. JIA was the most common initial diagnosis. The definitive diagnosis was acute lymphoblastic leukemia (2 patients), M3 acute myeloid leukemia, lymphoma, and neuroblastoma (one case each). Of 5 patients studied, 3 (60%) are in remission and 2 (40%) died, one of them with prior use of steroids.
The constitutional and musculoskeletal symptoms common to rheumatic and neoplastic diseases can delay the diagnosis and consequently worsen the prognosis of neoplasms. Initial blood count and bone marrow smear may be normal in the initial framework of neoplasms. Thus, the clinical follow-up of these cases becomes imperative and the treatment, mainly with corticosteroids, should be delayed until diagnostic definition.
Avaliar a prevalência e descrever as principais manifestações clínicas, exames complementares, tratamento e evolução de crianças com doenças neoplásicas atendidas inicialmente em um serviço terciário de reumatologia pediátrica.
Analisamos retrospectivamente o prontuário médico de pacientes com diagnóstico definitivo de neoplasia, identificados entre 250 casos novos atendidos no ambulatório de reumatologia pediátrica do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto-USP, no período de julho de 2013 a julho de 2015.
Dos 250 pacientes recebidos pelo ambulatório no período do estudo, 5 (2%) tiveram diagnóstico de neoplasia. Desses 5 pacientes, 80% apresentavam sintomas constitucionais, principalmente perda de peso e astenia e 60% artrite. Inicialmente, todos apresentavam pelo menos uma série alterada no hemograma, 80% aumento da desidrogenase lática (LDH) e 60% mielograma confirmatório. Dois pacientes necessitaram de biópsia, óssea e intestino, para o diagnóstico final. Artrite idiopática juvenil foi o diagnóstico inicial mais frequente. Os diagnósticos definitivos foram leucemia linfóide aguda (2 casos), leucemia mielóide aguda-M3, neuroblastoma e linfoma (1 caso cada). Dos pacientes estudados 3 (60%) estão em remissão. Dois pacientes foram a óbito (40%), um deles com uso prévio de corticoide.
Os sintomas constitucionais e musculoesqueléticos comuns às doenças reumáticas e neoplásicas podem retardar o diagnóstico e consequentemente agravar o prognóstico das neoplasias. O hemograma inicial, assim como o mielograma, podem estar normais no quadro inicial das neoplasias. Dessa forma, o seguimento clínico evolutivo destes casos torna-se imperativo e o tratamento, principalmente com corticoides, deve ser retardado até definição diagnóstica.</description><subject>Arthralgia - etiology</subject><subject>Artrite idiopática juvenil</subject><subject>Asthenia - etiology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Diagnosis, Differential</subject><subject>Doenças reumáticas, Pediatria</subject><subject>Female</subject><subject>Humans</subject><subject>Juvenile idiopathic arthritis</subject><subject>Male</subject><subject>Musculoskeletal symptoms</subject><subject>Neoplasia</subject><subject>Neoplasms - diagnosis</subject><subject>Neoplasms - physiopathology</subject><subject>Neoplastic diseases</subject><subject>Pediatric rheumatic disease</subject><subject>Retrospective Studies</subject><subject>Rheumatic Diseases - diagnosis</subject><subject>Rheumatic Diseases - physiopathology</subject><subject>Sintomas musculoesqueléticos</subject><issn>2255-5021</issn><issn>1809-4570</issn><issn>2255-5021</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>DOA</sourceid><recordid>eNp9kc1u1DAUhS0EolXpC7BAWbKZ9NqO7Qxig6oClSqxANbWHftm8CiJg51BmrfHaYaqK1b--86x7jmMveVQc-D65lCnXaJaADc18BrAvGCXQii1USD4y2f7C3ad8wGgkI0QEl6zC9GaRkoNl-z0PezHXOHoq3wapjkOuYpdlX7RccA5uMqHTJipILnqQspzNeAYOspzeY7jAk_kA86pwA5HR-lDEeF-jDmsxlOK51MYpj64R2F-w1512Ge6Pq9X7Ofnux-3XzcP377c33562DipwGw4tI1BgpZr7xCdU40XnSbnFQrVqu0WjZYNSONQkyGDftsZv9NSeOW6Rl6x-9XXRzzYKYUB08lGDPbxIqa9xVQm7clqvzPStFyQlE0jdGukU847g0AkzeL1fvUqI_0-lgzsELKjvseR4jFbvhULpk1bULGiLsWcE3VPX3OwS4P2YJcG7dKgBW5Lg0X07ux_3A3knyT_-irAxxWgktifQMlmF6iE7kMiN5eRwv_8_wLKFK4q</recordid><startdate>201707</startdate><enddate>201707</enddate><creator>Fonseca, Mariana Bertoldi</creator><creator>Gomes, Francisco Hugo Rodrigues</creator><creator>Valera, Elvis Terci</creator><creator>Pileggi, Gecilmara Salviato</creator><creator>Gonfiantini, Paula Braga</creator><creator>Gonfiantini, Marcela Braga</creator><creator>Ferriani, Virgínia Paes Leme</creator><creator>Carvalho, Luciana Martins de</creator><general>Elsevier Editora Ltda</general><general>Sociedade Brasileira de Reumatologia</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>DOA</scope></search><sort><creationdate>201707</creationdate><title>Signs and symptoms of rheumatic diseases as first manifestation of pediatric cancer: diagnosis and prognosis implications</title><author>Fonseca, Mariana Bertoldi ; Gomes, Francisco Hugo Rodrigues ; Valera, Elvis Terci ; Pileggi, Gecilmara Salviato ; Gonfiantini, Paula Braga ; Gonfiantini, Marcela Braga ; Ferriani, Virgínia Paes Leme ; Carvalho, Luciana Martins de</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3507-10847ae0816dcaacc54d2f6ecd5a258599a7634037ca6e7e7ad9f7db632d5cf43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Arthralgia - etiology</topic><topic>Artrite idiopática juvenil</topic><topic>Asthenia - etiology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Diagnosis, Differential</topic><topic>Doenças reumáticas, Pediatria</topic><topic>Female</topic><topic>Humans</topic><topic>Juvenile idiopathic arthritis</topic><topic>Male</topic><topic>Musculoskeletal symptoms</topic><topic>Neoplasia</topic><topic>Neoplasms - diagnosis</topic><topic>Neoplasms - physiopathology</topic><topic>Neoplastic diseases</topic><topic>Pediatric rheumatic disease</topic><topic>Retrospective Studies</topic><topic>Rheumatic Diseases - diagnosis</topic><topic>Rheumatic Diseases - physiopathology</topic><topic>Sintomas musculoesqueléticos</topic><toplevel>online_resources</toplevel><creatorcontrib>Fonseca, Mariana Bertoldi</creatorcontrib><creatorcontrib>Gomes, Francisco Hugo Rodrigues</creatorcontrib><creatorcontrib>Valera, Elvis Terci</creatorcontrib><creatorcontrib>Pileggi, Gecilmara Salviato</creatorcontrib><creatorcontrib>Gonfiantini, Paula Braga</creatorcontrib><creatorcontrib>Gonfiantini, Marcela Braga</creatorcontrib><creatorcontrib>Ferriani, Virgínia Paes Leme</creatorcontrib><creatorcontrib>Carvalho, Luciana Martins de</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Revista Brasileira de Reumatologia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fonseca, Mariana Bertoldi</au><au>Gomes, Francisco Hugo Rodrigues</au><au>Valera, Elvis Terci</au><au>Pileggi, Gecilmara Salviato</au><au>Gonfiantini, Paula Braga</au><au>Gonfiantini, Marcela Braga</au><au>Ferriani, Virgínia Paes Leme</au><au>Carvalho, Luciana Martins de</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Signs and symptoms of rheumatic diseases as first manifestation of pediatric cancer: diagnosis and prognosis implications</atitle><jtitle>Revista Brasileira de Reumatologia</jtitle><addtitle>Rev Bras Reumatol Engl Ed</addtitle><date>2017-07</date><risdate>2017</risdate><volume>57</volume><issue>4</issue><spage>330</spage><epage>337</epage><pages>330-337</pages><issn>2255-5021</issn><issn>1809-4570</issn><eissn>2255-5021</eissn><abstract>To assess the prevalence and describe the clinical, laboratory and radiological findings, treatment and outcome of children with cancer initially referred to a tertiary outpatient pediatric rheumatology clinic.
Retrospective analysis of medical records from patients identified in a list of 250 new patients attending the tertiary Pediatric Rheumatology Clinic, Ribeirão Preto Medical School hospital, University of São Paulo, from July 2013 to July 2015, whose final diagnosis was cancer.
Of 250 patients seen during the study period, 5 (2%) had a cancer diagnosis. Among them, 80% had constitutional symptoms, especially weight loss and asthenia, and 60% had arthritis. Initially, all patients had at least one alteration in their blood count, lactate dehydrogenase was increased in 80% and a bone marrow smear was conclusive in 60% of patients. Bone and intestine biopsies were necessary for the diagnosis in 2 patients. JIA was the most common initial diagnosis. The definitive diagnosis was acute lymphoblastic leukemia (2 patients), M3 acute myeloid leukemia, lymphoma, and neuroblastoma (one case each). Of 5 patients studied, 3 (60%) are in remission and 2 (40%) died, one of them with prior use of steroids.
The constitutional and musculoskeletal symptoms common to rheumatic and neoplastic diseases can delay the diagnosis and consequently worsen the prognosis of neoplasms. Initial blood count and bone marrow smear may be normal in the initial framework of neoplasms. Thus, the clinical follow-up of these cases becomes imperative and the treatment, mainly with corticosteroids, should be delayed until diagnostic definition.
Avaliar a prevalência e descrever as principais manifestações clínicas, exames complementares, tratamento e evolução de crianças com doenças neoplásicas atendidas inicialmente em um serviço terciário de reumatologia pediátrica.
Analisamos retrospectivamente o prontuário médico de pacientes com diagnóstico definitivo de neoplasia, identificados entre 250 casos novos atendidos no ambulatório de reumatologia pediátrica do Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto-USP, no período de julho de 2013 a julho de 2015.
Dos 250 pacientes recebidos pelo ambulatório no período do estudo, 5 (2%) tiveram diagnóstico de neoplasia. Desses 5 pacientes, 80% apresentavam sintomas constitucionais, principalmente perda de peso e astenia e 60% artrite. Inicialmente, todos apresentavam pelo menos uma série alterada no hemograma, 80% aumento da desidrogenase lática (LDH) e 60% mielograma confirmatório. Dois pacientes necessitaram de biópsia, óssea e intestino, para o diagnóstico final. Artrite idiopática juvenil foi o diagnóstico inicial mais frequente. Os diagnósticos definitivos foram leucemia linfóide aguda (2 casos), leucemia mielóide aguda-M3, neuroblastoma e linfoma (1 caso cada). Dos pacientes estudados 3 (60%) estão em remissão. Dois pacientes foram a óbito (40%), um deles com uso prévio de corticoide.
Os sintomas constitucionais e musculoesqueléticos comuns às doenças reumáticas e neoplásicas podem retardar o diagnóstico e consequentemente agravar o prognóstico das neoplasias. O hemograma inicial, assim como o mielograma, podem estar normais no quadro inicial das neoplasias. Dessa forma, o seguimento clínico evolutivo destes casos torna-se imperativo e o tratamento, principalmente com corticoides, deve ser retardado até definição diagnóstica.</abstract><cop>Brazil</cop><pub>Elsevier Editora Ltda</pub><pmid>28743360</pmid><doi>10.1016/j.rbre.2017.01.007</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Arthralgia - etiology Artrite idiopática juvenil Asthenia - etiology Child Child, Preschool Diagnosis, Differential Doenças reumáticas, Pediatria Female Humans Juvenile idiopathic arthritis Male Musculoskeletal symptoms Neoplasia Neoplasms - diagnosis Neoplasms - physiopathology Neoplastic diseases Pediatric rheumatic disease Retrospective Studies Rheumatic Diseases - diagnosis Rheumatic Diseases - physiopathology Sintomas musculoesqueléticos |
title | Signs and symptoms of rheumatic diseases as first manifestation of pediatric cancer: diagnosis and prognosis implications |
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