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Guideline for management of non-Down syndrome neonates with a myeloproliferative disease on behalf of the I-BFM AML Study Group and EWOG-MDS

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00064203%3A_____%2F22%3A10441721" target="_blank" >RIV/00064203:_____/22:10441721 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=QcdJsj8oTc" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=QcdJsj8oTc</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3324/haematol.2021.279507" target="_blank" >10.3324/haematol.2021.279507</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Guideline for management of non-Down syndrome neonates with a myeloproliferative disease on behalf of the I-BFM AML Study Group and EWOG-MDS

  • Popis výsledku v původním jazyce

    In neonates with myeloid hyperproliferation, apart from benign causes, Down syndrome (DS) related transient abnormal myelopoiesis (TAM), acute myeloid leukemia (AML) and juvenile myelomonocytic leukemia (JMML) are considered. Besides TAM, rarely, non-DS related transient myeloproliferative diseases occur, making clinical decisions challenging.4 TAM, according to World Health Organization (WHO) classification, only applies to children with (mosaic) Down syndrome.5 In the past, different terminology has been used in non-DS patients, such as transient myeloproliferative disease (TMD) and transient leukemia. Since distinction from TAM is important, and it is challenging to determine whether this disease will be transient, the consensus group introduced the novel term &apos;infantile myeloproliferative disease&apos; (IMD), in order to distinguish it from TAM. Both TAM and IMD can usually be managed with a &apos;watch and wait&apos; strategy, while most fullblown AML or JMML cases require intensive treatment. We collected rare IMD cases from study groups collaborating in the International Berlin-Frankfurt-Münster AML Study Group (I-BFM AML SG). In addition, we reviewed the literature for neonatal cases of malignant myeloid hyperproliferation without DS. Based on these data, we developed, together with I-BFM AML SG and the European Working Group of Myelodysplastic syndromes in Childhood (EWOG-MDS) members, by consensus, clinical recommendations for the diagnostic approach and current adequate classification of malignant myeloid hyperproliferation in infancy. This is meant guiding clinicians in choosing the right strategy, i.e., whether to &apos;watch and wait&apos; or start highly intensive treatment in individual cases.

  • Název v anglickém jazyce

    Guideline for management of non-Down syndrome neonates with a myeloproliferative disease on behalf of the I-BFM AML Study Group and EWOG-MDS

  • Popis výsledku anglicky

    In neonates with myeloid hyperproliferation, apart from benign causes, Down syndrome (DS) related transient abnormal myelopoiesis (TAM), acute myeloid leukemia (AML) and juvenile myelomonocytic leukemia (JMML) are considered. Besides TAM, rarely, non-DS related transient myeloproliferative diseases occur, making clinical decisions challenging.4 TAM, according to World Health Organization (WHO) classification, only applies to children with (mosaic) Down syndrome.5 In the past, different terminology has been used in non-DS patients, such as transient myeloproliferative disease (TMD) and transient leukemia. Since distinction from TAM is important, and it is challenging to determine whether this disease will be transient, the consensus group introduced the novel term &apos;infantile myeloproliferative disease&apos; (IMD), in order to distinguish it from TAM. Both TAM and IMD can usually be managed with a &apos;watch and wait&apos; strategy, while most fullblown AML or JMML cases require intensive treatment. We collected rare IMD cases from study groups collaborating in the International Berlin-Frankfurt-Münster AML Study Group (I-BFM AML SG). In addition, we reviewed the literature for neonatal cases of malignant myeloid hyperproliferation without DS. Based on these data, we developed, together with I-BFM AML SG and the European Working Group of Myelodysplastic syndromes in Childhood (EWOG-MDS) members, by consensus, clinical recommendations for the diagnostic approach and current adequate classification of malignant myeloid hyperproliferation in infancy. This is meant guiding clinicians in choosing the right strategy, i.e., whether to &apos;watch and wait&apos; or start highly intensive treatment in individual cases.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    30205 - Hematology

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2022

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Haematologica

  • ISSN

    0390-6078

  • e-ISSN

  • Svazek periodika

    107

  • Číslo periodika v rámci svazku

    3

  • Stát vydavatele periodika

    IT - Italská republika

  • Počet stran výsledku

    4006

  • Strana od-do

    759-4764

  • Kód UT WoS článku

    000811240400056

  • EID výsledku v databázi Scopus

    2-s2.0-85125554397