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Pre-analytical parameters associated with unsuccessful karyotyping in myeloid neoplasm: a study of 421 samples
Santos, M F M; Oliveira, F C A C; Kishimoto, R K; Borri, D; Santos, F P S; Campregher, P V; Silveira, P A A; Hamerschlak, N; Mangueira, C L P; Duarte, F B; Crepaldi, A H; Salvino, M A; Velloso, E D R P.
  • Santos, M F M; Hospital Israelita Albert Einstein. São Paulo. BR
  • Oliveira, F C A C; Hospital Israelita Albert Einstein. São Paulo. BR
  • Kishimoto, R K; Hospital Israelita Albert Einstein. São Paulo. BR
  • Borri, D; Hospital Israelita Albert Einstein. São Paulo. BR
  • Santos, F P S; Hospital Israelita Albert Einstein. São Paulo. BR
  • Campregher, P V; Hospital Israelita Albert Einstein. São Paulo. BR
  • Silveira, P A A; Hospital Israelita Albert Einstein. São Paulo. BR
  • Hamerschlak, N; Hospital Israelita Albert Einstein. São Paulo. BR
  • Mangueira, C L P; Hospital Israelita Albert Einstein. São Paulo. BR
  • Duarte, F B; Universidade Federal do Ceará. Hospital Universitário Walter Cantídio. Fortaleza. BR
  • Crepaldi, A H; Hospital de Câncer de Mato Grosso. Cuiabá. BR
  • Salvino, M A; Hospital São Rafael/Monte Tabor. Salvador. BR
  • Velloso, E D R P; Hospital Israelita Albert Einstein. São Paulo. BR
Braz. j. med. biol. res ; 52(2): e8194, 2019.
Article in English | LILACS | ID: biblio-984032
ABSTRACT
Cytogenetics is essential in myeloid neoplasms (MN) and pre-analytical variables are important for karyotyping. We assessed the relationship between pre-analytical variables (time from collection to sample processing, material type, sample cellularity, and diagnosis) and failures of karyotyping. Bone marrow (BM, n=352) and peripheral blood (PB, n=69) samples were analyzed from acute myeloid leukemia (n=113), myelodysplastic syndromes (n=73), myelodysplastic syndromes/myeloproliferative neoplasms (n=17), myeloproliferative neoplasms (n=137), and other with conclusive diagnosis (n=6), and reactive disorders/no conclusive diagnosis (n=75). The rate of unsuccessful karyotyping was 18.5% and was associated with the use of PB and a low number of nucleated cells (≤7×103/µL) in the sample. High and low cellularity in BM and high and low cellularity in PB samples showed no metaphases in 3.9, 39.7, 41.9, and 84.6% of cases, respectively. Collecting a good BM sample is the key for the success of karyotyping in MN and avoids the use of expensive molecular techniques.
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Full text: Available Index: LILACS (Americas) Main subject: Specimen Handling / Myelodysplastic Syndromes / Bone Marrow Cells / Leukemia, Myeloid / Karyotyping / Myeloproliferative Disorders Type of study: Diagnostic study / Risk factors Limits: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2019 Type: Article Affiliation country: Brazil Institution/Affiliation country: Hospital Israelita Albert Einstein/BR / Monte Tabor+BR / Hospital de Câncer de Mato Grosso/BR / Universidade Federal do Ceará/BR

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Full text: Available Index: LILACS (Americas) Main subject: Specimen Handling / Myelodysplastic Syndromes / Bone Marrow Cells / Leukemia, Myeloid / Karyotyping / Myeloproliferative Disorders Type of study: Diagnostic study / Risk factors Limits: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male Language: English Journal: Braz. j. med. biol. res Journal subject: Biology / Medicine Year: 2019 Type: Article Affiliation country: Brazil Institution/Affiliation country: Hospital Israelita Albert Einstein/BR / Monte Tabor+BR / Hospital de Câncer de Mato Grosso/BR / Universidade Federal do Ceará/BR