Successful reduced-intensity stem cell transplantation for GATA2 deficiency before progression of advanced MDS.
Identifieur interne : 007D27 ( Ncbi/Curation ); précédent : 007D26; suivant : 007D28Successful reduced-intensity stem cell transplantation for GATA2 deficiency before progression of advanced MDS.
Auteurs : Satoshi Saida [Japon] ; Katsutsugu Umeda [Japon] ; Takahiro Yasumi [Japon] ; Akane Matsumoto [Japon] ; Itaru Kato [Japon] ; Hidefumi Hiramatsu [Japon] ; Osamu Ohara [Japon] ; Toshio Heike [Japon] ; Souichi Adachi [Japon]Source :
- Pediatric transplantation [ 1399-3046 ] ; 2016.
Descripteurs français
- KwdFr :
- Adolescent, Adulte, Adulte d'âge moyen, Analyse de séquence d'ADN, Antigènes HLA (génétique), Caryotypage, Cellules de la moelle osseuse (cytologie), Facteur de transcription GATA-2 (déficit), Femelle, Humains, Japon, Mutation, Mâle, Pedigree, Phénotype, Pédiatrie, Résultat thérapeutique, Syndromes myélodysplasiques (), Transplantation de cellules souches, Évolution de la maladie.
- MESH :
- cytologie : Cellules de la moelle osseuse.
- déficit : Facteur de transcription GATA-2.
- génétique : Antigènes HLA.
- Adolescent, Adulte, Adulte d'âge moyen, Analyse de séquence d'ADN, Caryotypage, Femelle, Humains, Japon, Mutation, Mâle, Pedigree, Phénotype, Pédiatrie, Résultat thérapeutique, Syndromes myélodysplasiques, Transplantation de cellules souches, Évolution de la maladie.
English descriptors
- KwdEn :
- Adolescent, Adult, Bone Marrow Cells (cytology), Disease Progression, Female, GATA2 Transcription Factor (deficiency), HLA Antigens (genetics), Humans, Japan, Karyotyping, Male, Middle Aged, Mutation, Myelodysplastic Syndromes (therapy), Pediatrics, Pedigree, Phenotype, Sequence Analysis, DNA, Stem Cell Transplantation, Treatment Outcome.
- MESH :
- chemical , deficiency : GATA2 Transcription Factor.
- cytology : Bone Marrow Cells.
- chemical , genetics : HLA Antigens.
- therapy : Myelodysplastic Syndromes.
- Adolescent, Adult, Disease Progression, Female, Humans, Japan, Karyotyping, Male, Middle Aged, Mutation, Pediatrics, Pedigree, Phenotype, Sequence Analysis, DNA, Stem Cell Transplantation, Treatment Outcome.
Abstract
A 13-yr-old boy bearing lymphedema and congenital deafness had distinct hematological abnormalities consisting of reduced monocytes, B cells, and dendritic cells in the peripheral blood as well as MDS with normal karyotype in the bone marrow. The patient was diagnosed with Emberger syndrome by sequencing of GATA2 DNA, and underwent RIST from an HLA-matched unrelated donor. Prompt engraftment and immunological reconstitution were observed without any severe RRT. As most patients with GATA2 anomaly died due to the development of AML or active infections, RIST could be a promising treatment option before progression of advanced MDS.
DOI: 10.1111/petr.12667
PubMed: 26748574
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pubmed:26748574Le document en format XML
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<term>Adult</term>
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<term>Female</term>
<term>GATA2 Transcription Factor (deficiency)</term>
<term>HLA Antigens (genetics)</term>
<term>Humans</term>
<term>Japan</term>
<term>Karyotyping</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Mutation</term>
<term>Myelodysplastic Syndromes (therapy)</term>
<term>Pediatrics</term>
<term>Pedigree</term>
<term>Phenotype</term>
<term>Sequence Analysis, DNA</term>
<term>Stem Cell Transplantation</term>
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<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Analyse de séquence d'ADN</term>
<term>Antigènes HLA (génétique)</term>
<term>Caryotypage</term>
<term>Cellules de la moelle osseuse (cytologie)</term>
<term>Facteur de transcription GATA-2 (déficit)</term>
<term>Femelle</term>
<term>Humains</term>
<term>Japon</term>
<term>Mutation</term>
<term>Mâle</term>
<term>Pedigree</term>
<term>Phénotype</term>
<term>Pédiatrie</term>
<term>Résultat thérapeutique</term>
<term>Syndromes myélodysplasiques ()</term>
<term>Transplantation de cellules souches</term>
<term>Évolution de la maladie</term>
</keywords>
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</keywords>
<keywords scheme="MESH" qualifier="déficit" xml:lang="fr"><term>Facteur de transcription GATA-2</term>
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<term>Disease Progression</term>
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<term>Humans</term>
<term>Japan</term>
<term>Karyotyping</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Mutation</term>
<term>Pediatrics</term>
<term>Pedigree</term>
<term>Phenotype</term>
<term>Sequence Analysis, DNA</term>
<term>Stem Cell Transplantation</term>
<term>Treatment Outcome</term>
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<term>Adulte</term>
<term>Adulte d'âge moyen</term>
<term>Analyse de séquence d'ADN</term>
<term>Caryotypage</term>
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<term>Humains</term>
<term>Japon</term>
<term>Mutation</term>
<term>Mâle</term>
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<term>Pédiatrie</term>
<term>Résultat thérapeutique</term>
<term>Syndromes myélodysplasiques</term>
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<term>Évolution de la maladie</term>
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<front><div type="abstract" xml:lang="en">A 13-yr-old boy bearing lymphedema and congenital deafness had distinct hematological abnormalities consisting of reduced monocytes, B cells, and dendritic cells in the peripheral blood as well as MDS with normal karyotype in the bone marrow. The patient was diagnosed with Emberger syndrome by sequencing of GATA2 DNA, and underwent RIST from an HLA-matched unrelated donor. Prompt engraftment and immunological reconstitution were observed without any severe RRT. As most patients with GATA2 anomaly died due to the development of AML or active infections, RIST could be a promising treatment option before progression of advanced MDS.</div>
</front>
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