A Rare der(Y)t(Y;1)(q12;q12) in a Patient with Essential Thrombocythemia
Laboratory Medicine Online
;
: 183-186, 2016.
Article
Dans Coréen
| WPRIM
| ID: wpr-171889
ABSTRACT
Among hematologic diseases, structural abnormalities of autosomal chromosomes are well-known, but cases involving the sex chromosomes are uncommon. Duplications of the long arm of chromosome 1 have been reported in several hematologic diseases including myelodysplastic syndrome, myeloproliferative neoplasms, acute myeloid leukemia, acute lymphoblastic leukemia, and Burkitt lymphoma. However, dup(1q) as a der(Y)t(Y;1)(q12;q12) is very rare. Here, we report a case of essential thrombocythemia harboring der(Y)t(Y;1)(q12;q12) with literature review.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Bras
/
Chromosomes sexuels
/
Syndromes myélodysplasiques
/
Chromosomes humains de la paire 1
/
Leucémie aigüe myéloïde
/
Aberrations des chromosomes
/
Lymphome de Burkitt
/
Leucémie-lymphome lymphoblastique à précurseurs B et T
/
Hémopathies
/
Thrombocytémie essentielle
Limites du sujet:
Humains
langue:
Coréen
Texte intégral:
Laboratory Medicine Online
Année:
2016
Type:
Article
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