Riccardi V M, Humbert J R, Peakman D
Am J Med Genet. 1978;2(1):15-21. doi: 10.1002/ajmg.1320020104.
A patient is shown to have acute granulocytic leukemia, bone marrow mosaicism, and cutaneous fibroblast mosaicism for trisomy 8, an inherited reciprocal translocation involving the short arms of chromosomes 7 and 20, and a family history of cancer. A normal sister who had the same balanced chromosome translocation was evaluated for a preleukemic state; the results were unremarkable. The inherited translocation and postzygotically derived trisomy 8 are thought to represent additive factors contributing to the development of leukemia in the patient.
一名患者被诊断患有急性粒细胞白血病、骨髓嵌合体以及8号染色体三体的皮肤成纤维细胞嵌合体,其携带涉及7号和20号染色体短臂的遗传性相互易位,并有癌症家族史。对一名具有相同平衡染色体易位的正常姐妹进行了白血病前期评估,结果无异常。遗传性易位和合子后衍生的8号染色体三体被认为是导致该患者白血病发生的累加因素。