三体8
三体
生物
白塞病
恶性肿瘤
染色体易位
骨髓增生异常综合症
非整倍体
免疫学
唐氏综合症
疾病
癌症研究
内科学
遗传学
细胞遗传学
染色体
医学
骨髓
基因
作者
Sachiko Ando,Masayo Maemori,Hajime Sakai,Seisho Ando,Hideaki Shiraishi,Keisuke Sakai,Gregory W. Ruhnke
标识
DOI:10.1016/j.cancergencyto.2005.01.010
摘要
Trisomy 8 is the most common acquired chromosomal abnormality associated with myeloid malignancy. As a constitutional trisomy 8 mosaicism (T8M), it exhibits an extremely variable phenotype. In addition, Behcet disease (BD) has been reported as an unusual complication of myelodysplastic syndrome (MDS). To our knowledge, 12 case reports of various hematologic malignancies in patients with T8M and 18 case reports of MDS with acquired trisomy 8 complicated by BD have been published to date. We report a case of constitutional T8M with MDS complicated by intestinal BD and antithrombin III deficiency.
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