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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.
Affiliation
  • Santos MFM; Hospital Israelita Albert Einstein, São Paulo, SP, Brasil.
  • Oliveira FCAC; Hospital Israelita Albert Einstein, São Paulo, SP, Brasil.
  • Kishimoto RK; Hospital Israelita Albert Einstein, São Paulo, SP, Brasil.
  • Borri D; Hospital Israelita Albert Einstein, São Paulo, SP, Brasil.
  • Santos FPS; Hospital Israelita Albert Einstein, São Paulo, SP, Brasil.
  • Campregher PV; Hospital Israelita Albert Einstein, São Paulo, SP, Brasil.
  • Silveira PAA; Hospital Israelita Albert Einstein, São Paulo, SP, Brasil.
  • Hamerschlak N; Hospital Israelita Albert Einstein, São Paulo, SP, Brasil.
  • Mangueira CLP; Hospital Israelita Albert Einstein, São Paulo, SP, Brasil.
  • Duarte FB; Hospital Universitário Walter Cantídio, Universidade Federal do Ceará, Fortaleza, CE, Brasil.
  • Crepaldi AH; Hospital de Câncer de Mato Grosso, Cuiabá, MT, Brasil.
  • Salvino MA; Hospital São Rafael/Monte Tabor, Salvador, BA, Brasil.
  • Velloso EDRP; Hospital Israelita Albert Einstein, São Paulo, SP, Brasil.
Braz J Med Biol Res ; 52(2): e8194, 2019 Feb 14.
Article in En | MEDLINE | ID: mdl-30785480
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Specimen Handling / Myelodysplastic Syndromes / Bone Marrow Cells / Leukemia, Myeloid / Karyotyping / Myeloproliferative Disorders Type of study: Diagnostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Braz J Med Biol Res Year: 2019 Document type: Article Affiliation country: Brazil

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Specimen Handling / Myelodysplastic Syndromes / Bone Marrow Cells / Leukemia, Myeloid / Karyotyping / Myeloproliferative Disorders Type of study: Diagnostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Braz J Med Biol Res Year: 2019 Document type: Article Affiliation country: Brazil
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