A Rare der(Y)t(Y;1)(q12;q12) in a Patient with Essential Thrombocythemia
Laboratory Medicine Online
; : 183-186, 2016.
Article
em Ko
| WPRIM
| ID: wpr-171889
Biblioteca responsável:
WPRO
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.
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Índice:
WPRIM
Assunto principal:
Braço
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Cromossomos Sexuais
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Síndromes Mielodisplásicas
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Cromossomos Humanos Par 1
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Leucemia Mieloide Aguda
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Aberrações Cromossômicas
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Linfoma de Burkitt
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Leucemia-Linfoma Linfoblástico de Células Precursoras
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Doenças Hematológicas
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Trombocitemia Essencial
Limite:
Humans
Idioma:
Ko
Revista:
Laboratory Medicine Online
Ano de publicação:
2016
Tipo de documento:
Article