Brazilian Journal of Pathology and Laboratory Medicine

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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

Article Type, Issue, Review Article, Vol 54, Issue 2 /

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

Review Article /

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

Article Type, Case Report, Issue, Vol 54, Issue 2 /

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 »

Underreporting of scientific knowledge: a theme for reflection

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

Case Report /

Trombofilia hereditária por mutações G1691A do fator V Leiden (heterozigota) e G20210A do FII protrombina (homozigota) em paciente com acidente vascular cerebral isquêmico Leonardo G. P. Ruiz; Maria Gabriela L. Oliveira; Adriana L. Z. Ruiz; Camila S. Daher; Mauricio L. Nogueira Fundação Faculdade Regional de Medicina de São José do Rio Preto (FUNFARME), São Paulo,

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

hyroid (HE, 40×): intense lymphocytic infiltrate diffusely associated with adipose tissue sparse within the parenchyma

Adipose metaplasia of the thyroid associated with Hashimoto’s thyroiditis with nodular hyperplasia and oncocytic cells adenoma: case report and literature review

Article Type, Case Report, Issue, Vol 54, Issue 2 /

Andrey Biff Sarris; Matheus A. Santos; Rubens Adão da Silva; Mário R. Montemor NettoJ. Bras. Patol. Med. Lab. 2018;54(2):105-108DOI:10.5935/1676-2444.20180019 RESUMO Lesões que envolvem tecido adiposo e glândula tireoide costumam ser raros. No presente relato, a metaplasia adiposa associou-se à tireoidite de Hashimoto com hiperplasia nodular e adenoma de células oncocíticas em uma paciente de 40

Adipose metaplasia of the thyroid associated with Hashimoto’s thyroiditis with nodular hyperplasia and oncocytic cells adenoma: case report and literature review Read More »

Underreporting of scientific knowledge: a theme for reflection

Adipose metaplasia of the thyroid associated with Hashimoto’s thyroiditis with nodular hyperplasia and oncocytic cells adenoma: case report and literature review

Case Report /

Metaplasia adiposa de tireoide associada à tireoidite de Hashimoto com hiperplasia nodular e adenoma de células oncocíticas: relato de caso e revisão da literatura Andrey Biff Sarris1; Matheus A. Santos1; Rubens Adão da Silva2; Mário R. Montemor Netto1 1. Universidade Estadual de Ponta Grossa (UEPG), Paraná, Brazil2. Instituto Sul Paranaense de Oncologia (ISPON), Paraná, Brazil

Adipose metaplasia of the thyroid associated with Hashimoto’s thyroiditis with nodular hyperplasia and oncocytic cells adenoma: case report and literature review Read More »

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

Autopsy findings of a child with left atrial isomerism associated with pulmonary agenesis

Article Type, Case Report, Issue, Vol 54, Issue 2 /

Camilla M. V. Pereira; Larissa V. Cruz; Marina C. Girotto; André C. Cunha; Jorge Alberto B. Telles; Bruna L. Diniz; Rosana C. M. Rosa; Paulo Ricardo G. Zen; Rafael Fabiano M. RosaJ. Bras. Patol. Med. Lab. 2018;54(2):109-110DOI:10.5935/1676-2444.20180020 RESUMO O isomerismo é um defeito de lateralidade raro. Nosso objetivo foi descrever os achados da autópsia de

Autopsy findings of a child with left atrial isomerism associated with pulmonary agenesis Read More »

Underreporting of scientific knowledge: a theme for reflection

Autopsy findings of a child with left atrial isomerism associated with pulmonary agenesis

Case Report /

Achados de autópsia de uma criança com isomerismo atrial esquerdo associado à agenesia pulmonar Camilla M. V. Pereira1; Larissa V. Cruz1; Marina C. Girotto1; André C. Cunha2; Jorge Alberto B. Telles2; Bruna L. Diniz1; Rosana C. M. Rosa1; Paulo Ricardo G. Zen1,3; Rafael Fabiano M. Rosa1-3 1. Universidade Federal de Ciências da Saúde de Porto

Autopsy findings of a child with left atrial isomerism associated with pulmonary agenesis Read More »

Histological sections stained with HE

Chondroblastic osteosarcoma of the mandible: case report

Article Type, Case Report, Issue, Vol 54, Issue 2 /

Loara Gabriela R. Oliveira; John Lennon S. Cunha; Bruno T. Bezerra; Maria de Fátima B. Melo; Juliana B. M. Fonte; Ricardo Luiz C. Albuquerque Jr.J. Bras. Patol. Med. Lab. 2018;54(2):111-115DOI:10.5935/1676-2444.20180021 RESUMO Relatamos o caso de um paciente do sexo masculino, 32 anos de idade, que realizou tomografia cone-beam para planejamento de remoção de dente incluso.

Chondroblastic osteosarcoma of the mandible: case report Read More »

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

Chondroblastic osteosarcoma of the mandible: case report

Case Report /

Osteossarcoma condroblástico em mandíbula: relato de caso Loara Gabriela R. Oliveira1; John Lennon S. Cunha1; Bruno T. Bezerra1; Maria de Fátima B. Melo2; Juliana B. M. Fonte2; Ricardo Luiz C. Albuquerque Jr.1 1. Universidade Tiradentes, Sergipe, Brazil2. Universidade Federal de Sergipe, Sergipe, Brazil Endereço para correspondência John Lennon Silva CunhaRua João Geniton da Costa, 501;

Chondroblastic osteosarcoma of the mandible: case report Read More »