AN ATYPICAL MYELOPROLIFERATIVE DISORDER WITH T(8-13)(P11-Q12) - A 3RD CASE

被引：47

作者：

MACDONALD, D ^{[1
]}

SHEERIN, SM ^{[1
]}

CROSS, NCP ^{[1
]}

SPENCER, A ^{[1
]}

GOLDMAN, JM ^{[1
]}

机构：

[1] STOKE MANDEVILLE HOSP,DEPT HAEMATOL,AYLESBURY HP21 8AL,BUCKS,ENGLAND

来源：

BRITISH JOURNAL OF HAEMATOLOGY | 1994年 / 86卷 / 04期

关键词：

MYELOPROLIFERATIVE; CHRONIC; CLONAL; LEUKEMIA; T(813);

D O I：

10.1111/j.1365-2141.1994.tb04848.x

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

A 43-year-old male presented with a myeloproliferative disorder with prominent lymphadenopathy. Examination of the bone marrow showed almost complete replacement by a population of cells with an acquired chromosomal translocation t(8;13)(p11;q12). There are two other case reports describing a similar clinical syndrome with t(8;13)(p11;q12) as the sole chromosomal aberration in bone marrow cells, suggesting a role for this translocation in the pathogenesis of this myeloproliferative disorder.

引用

页码：879 / 880

页数：2

共 9 条

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