Brazilian Journal of Pathology and Laboratory Medicine

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Palisaded encapsulated neuroma clinically mimicking a mucocele: report of a case

Neuroma encapsulado em paliçada mimetizando mucocele: relato de caso John Lennon S. Cunha1; Amanda F. Silva1; Raimundo S. Rocha1; Ericka Janine D. Silveira2; Ricardo Luiz C. Albuquerque Jr.1 1. Universidade Tiradentes (Unit), Sergipe, Brazil2. Universidade Federal do Rio Grande do Norte (UFRN), Rio Grande do Norte, Brazil Endereço para correspondência John Lennon Silva CunhaRua João […]

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Evaluation of TP53 Gene Expression in Patients with Childhood Cancer in Northeast Santa Catarina, Brazil

Standards for the diagnosis and treatment of chronic myeloid leukemia

Paulo CampregherJ. Bras. Patol. Med. Lab. 2018;54(2):68DOI:10.5935/1676-2444.20180023 ABSTRACT Myeloproliferative disorders are a group of clonal myeloid neoplasms characterized by increased proliferation of myeloid cells with preserved cell differentiation. The molecular features of myeloproliferative neoplasms have been efficiently mapped in the last decades(1). Chronic myeloid leukemia (CML) is a myeloproliferative neoplasm defined by the presence of

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Evaluation of TP53 Gene Expression in Patients with Childhood Cancer in Northeast Santa Catarina, Brazil

Standards for the diagnosis and treatment of chronic myeloid leukemia

Paulo Campregher Laboratório de Genética Molecular do Hospital Israelita Albert Einstein, São Paulo, Brazil Myeloproliferative disorders are a group of clonal myeloid neoplasms characterized by increased proliferation of myeloid cells with preserved cell differentiation. The molecular features of myeloproliferative neoplasms have been efficiently mapped in the last decades(1). Chronic myeloid leukemia (CML) is a myeloproliferative

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Mean values of the concentrations of samples extracted by the two methods PKM: proteinase K method.

Comparison of DNA extraction using proteinase K and extraction kit: analysis of the quality of the genetic material

André Luís F. Santos; Carolina Q. P. Oliveira; Geovana Nicole P. N. Arruda; John Kenned MartinsJ. Bras. Patol. Med. Lab. 2018;54(2):70-75DOI:10.5935/1676-2444.20180013 RESUMO INTRODUÇÃO: O ácido desoxirribonucleico (DNA) é a matéria-prima para os estudos genéticos, por isso são desenvolvidas técnicas laboratoriais para sua obtenção, com concentração e integridades adequadas.OBJETIVO: Comparar dois métodos de extração de DNA em relação

Comparison of DNA extraction using proteinase K and extraction kit: analysis of the quality of the genetic material Read More »

Mean values of the concentrations of samples extracted by the two methods PKM: proteinase K method.

Comparison of DNA extraction using proteinase K and extraction kit: analysis of the quality of the genetic material

Comparação da extração de DNA utilizando proteinase K e kit de extração: análise da qualidade do material genético André Luís F. Santos; Carolina Q. P. Oliveira; Geovana Nicole P. N. Arruda; John Kenned Martins Fundação Instituto de Ensino de Barueri, São Paulo, Brazil Endereço para correspondência André Luís Fernandes dos SantosRua Terezina, 68; RochdalleCEP: 06226-100;

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Evaluation of TP53 Gene Expression in Patients with Childhood Cancer in Northeast Santa Catarina, Brazil

Prevalence and antimicrobial susceptibility profile of microorganisms in a university hospital from Vitória (ES), Brazil

Prevalência de microrganismos e perfil de suscetibilidade antimicrobiana em um hospital universitário de Vitória (ES), Brasil Carla C. M. Siqueira1; Alexandre C. Guimarães1; Thays F. D. Mata1; Rodrigo Pratte-Santos2,3; Norma Lucia S. Raymundo1; Carolina F. Dias4; Rodrigo Moraes1,3 1. Escola Superior de Ciências da Santa Casa de Misericórdia de Vitória (EMESCAM), Espírito Santo, Brazil2. Universidade

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Evaluation of TP53 Gene Expression in Patients with Childhood Cancer in Northeast Santa Catarina, Brazil

Prevalence and antimicrobial susceptibility profile of microorganisms in a university hospital from Vitória (ES), Brazil

Carla C. M. Siqueira; Alexandre C. Guimarães; Thays F. D. Mata; Rodrigo Pratte-Santos; Norma Lucia S. Raymundo; Carolina F. Dias; Rodrigo MoraesJ. Bras. Patol. Med. Lab. 2018;54(2):76-82DOI:10.5935/1676-2444.20180014 RESUMO INTRODUÇÃO: As infecções relacionadas com a assistência à saúde (IRAS) ocorrem durante a internação como resultado de morbidade subjacente, procedimentos invasivos, patologia aguda ou tratamento médico. Elas levam

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Translocation in the BCR-ABL1 gene

The role of cytogenetics and molecular biology in the diagnosis, treatment and monitoring of patients with chronic myeloid leukemia

Luiza Emy Dorfman; Maiara A. Floriani; Tyana Mara R. D. R. Oliveira; Bibiana Cunegatto; Rafael Fabiano M. Rosa; Paulo Ricardo G. ZenJ. Bras. Patol. Med. Lab. 2018;54(2):83-91DOI:10.5935/1676-2444.20180015 RESUMO Leucemia mieloide crônica (LMC) é a desordem mieloproliferativa mais comum entre as neoplasias crônicas. A história dessa doença se alia ao desenvolvimento de técnicas de análise citogenética

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Evaluation of TP53 Gene Expression in Patients with Childhood Cancer in Northeast Santa Catarina, Brazil

The role of cytogenetics and molecular biology in the diagnosis, treatment and monitoring of patients with chronic myeloid leukemia

O papel da citogenética e da biologia molecular no diagnóstico, no tratamento e no monitoramento de pacientes com leucemia mieloide crônica Luiza Emy Dorfman1; Maiara A. Floriani1; Tyana Mara R. D. R. Oliveira1; Bibiana Cunegatto1; Rafael Fabiano M. Rosa1,2; Paulo Ricardo G. Zen1,2 1. Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Rio

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Lateral chest X-ray. Opacity in right lung base and in midfields and left lung base, due to air space filling lesions

Hereditary thrombophilia by factor V Leiden G1691A (heterozygous) and FII prothrombin G20210A (homozygous) mutations in a patient with ischemic cerebrovascular accident

Leonardo G. P. Ruiz; Maria Gabriela L. Oliveira; Adriana L. Z. Ruiz; Camila S. Daher; Mauricio L. NogueiraJ. Bras. Patol. Med. Lab. 2018;54(2):92-94DOI:10.5935/1676-2444.20180016 RESUMO Mutações relacionadas com o fator V de Leiden (G1691A) e a protrombina (G20210A) estão associadas a um significativo aumento do risco de tromboembolismo venoso. Por meio da realização de exames moleculares

Hereditary thrombophilia by factor V Leiden G1691A (heterozygous) and FII prothrombin G20210A (homozygous) mutations in a patient with ischemic cerebrovascular accident Read More »