Macdonald D, Sheerin S M, Cross N C, Spencer A, Goldman J M
LRF Centre for Adult Leukaemia, Royal Postgraduate Medical School, Hammersmith Hospital, London.
Br J Haematol. 1994 Apr;86(4):879-80. doi: 10.1111/j.1365-2141.1994.tb04848.x.
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.
一名43岁男性因骨髓增殖性疾病伴显著淋巴结肿大就诊。骨髓检查显示,一群获得性染色体易位t(8;13)(p11;q12)的细胞几乎完全替代了骨髓。另外还有两篇病例报告描述了类似的临床综合征,t(8;13)(p11;q12)是骨髓细胞中唯一的染色体畸变,提示这种易位在该骨髓增殖性疾病的发病机制中起作用。