Haruta Y, Takahashi I, Sekito N, Miyamoto K, Shimamoto M, Wakita Y, Kikkawa K, Nakamura T, Seto T, Yamashita J
Department of Internal Medicine, Kochi Municipal Central Hospital, Japan.
Acta Med Okayama. 1990 Oct;44(5):283-6. doi: 10.18926/AMO/30448.
A rare case of variant Philadelphia (Ph1) chromosome positive [46, XX, t (9; 22) (q34; q11), inv (9) (9q22; 22q13)] chronic myelocytic leukemia (CML) was described. The patient, 73 years old female, was hospitalized to our hospital because of leukocytosis. Hematological findings corresponded to those of CMLs. However, this case lacked hepatosplenomegaly. Southern blot analysis using a 3 breakpoint cluster region (bcr) probe revealed a bcr rearrangement. The patient has been in the chronic phase for sixteen months without treatment. Clinical and chromosomal changes are under observation in order to get accumulate data for a pathophysiological analysis of variant Ph1 positive CMLs.
描述了一例罕见的变异型费城(Ph1)染色体阳性[46, XX, t(9; 22)(q34; q11), inv(9)(9q22; 22q13)]慢性粒细胞白血病(CML)病例。患者为73岁女性,因白细胞增多症入住我院。血液学检查结果与慢性粒细胞白血病相符。然而,该病例无肝脾肿大。使用3个断裂点簇集区(bcr)探针进行的Southern印迹分析显示存在bcr重排。该患者未经治疗已处于慢性期16个月。目前正在观察临床和染色体变化,以便积累数据用于变异型Ph1阳性慢性粒细胞白血病的病理生理分析。