Challenges in Diagnosing Myelodysplastic Syndromes in the Era of Genetic Testing: Proceedings of the 13th Workshop of the European Bone Marrow Working Group
Jazyk angličtina Země Švýcarsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
29982244
PubMed Central
PMC6482987
DOI
10.1159/000489678
PII: 000489678
Knihovny.cz E-zdroje
- Klíčová slova
- Bone marrow, Classification, Cytopenia, Myelodysplastic syndrome, Next-generation sequencing, Workshop,
- MeSH
- chromozomální aberace * MeSH
- dospělí MeSH
- genetické testování MeSH
- kostní dřeň patologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- myelodysplastické syndromy klasifikace diagnóza genetika patologie MeSH
- sekvenční analýza DNA MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- výchova a vzdělávání MeSH
- vysoce účinné nukleotidové sekvenování MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
The 13th workshop of the European Bone Marrow Working Group in Utrecht, The Netherlands, was devoted to studying myelodysplastic syndromes (MDS) and their boundaries. The panel received 44 cases submitted to the 3 invited categories, which included: reactive cytopenias with dysplasia, idiopathic cytopenia of undetermined significance, clonal haematopoiesis of indeterminate potential, idiopathic dysplasia of uncertain significance and overt MDS. For this summary, we have selected 17 cases that highlight difficulties in separating true MDS from other causes of cytopenia and the intricate relationship between clonal haematopoiesis and true MDS. In addition, cases of overt MDS with challenging features were also selected. All cases were stained for p53 expression. Using instructive submitted cases we discuss the following: (1) cytopenia with clonal haematopoiesis not fulfilling MDS criteria, (2) cytopenia and/or dysplasia with germline mutations and/or familial history suggesting an underlying gene defect, (3) MDS based on a recurrent chromosomal abnormality and (4) overt MDS with diagnostic difficulties due to concurrent treatment or disease. The lively discussion in the open forum of the workshop illustrated the need for better integrative understanding of the evolution of acquired genetic abnormalities in haematopoiesis, and the challenge of diagnosing true MDS in cytopenic patients with genetic abnormalities, either germline or acquired.
Department of Pathology and Cytology Karolinska University Hospital and Institute Stockholm Sweden
Department of Pathology and Laboratory Medicine Weill Cornell Medical College New York New York USA
Department of Pathology Charles University Hospital Pilsen Czech Republic
Department of Pathology Massachusetts General Hospital Boston Massachusetts USA
Department of Pathology Radboud University Medical Center Nijmegen The
Department of Pathology University Medical Center Utrecht Utrecht The Netherlands
Department of Pathology University of Tuebingen Tuebingen Germany
Institute of Pathology University Hospital Basel Basel Switzerland
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