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对一个胃肠道恶性疾病高易感性家族的医学遗传学和细胞遗传学研究。

Medico-genetic and cytogenetic study of a family with high predisposition to malignant disease in gastro-intestinal tract.

作者信息

Monakhov A S, Gulyaev A V, Savochkina I V, Hanson K P

机构信息

N.N. Petrov Research Institute of Oncology, St. Petersburg, Russia.

出版信息

J Exp Clin Cancer Res. 1997 Dec;16(4):385-8.

PMID:9505210
Abstract

In a family consisting of 48 persons with high predisposition to familial stomach cancer (SCr), SCr was diagnosed in 8 persons (I-2; II-1,3,4; III-1,2,3,4). Moreover, one woman (III-8) had bilateral breast cancer and two (proband: IV-1 and her father's cousin: III-10) chronic gastritis. The proband, her father's cousin, his sister (III-11) and the proband's sister (IV-2) were examined clinically and cytogenetically (with the metaphase method on blood lymphocytes with G-banding of chromosome 21: (p12-pter) in 100% of cells on the basis of chromosomal instability; besides, the complex translocation in chromosome 2 in 4% of cells and the increase of q-arm of chromosome 21 was found in 2% of cells. The proband's sister (IV-2) had 3% of cells with polyploidy, the del 1 (p34-pter) in 1% of cells and the del 7 (p21-pter) in 4% of cells. The cytogenetic examination of the proband's uncle (III-10), carried out 3 times, revealed the case of the proband, endomitosis in 2% of cells, polyploidy in 2% of cells and hyperaneuploidy in 4% of cells. His sister (III-11) had 4% of cells with endomitosis, 3% of cells with chromosome and chromatid breaches, an increase of the p-arm of chromosome 21 in 100% of cells and the loss of 7p in 2% of cells. The nature of the phenomenon in chromosome 21 and the translocations in the members of this family is here discussed. The cytogenetic examination is currently ongoing.

摘要

在一个由48名患家族性胃癌(SCr)高度易感性的人组成的家族中,8人被诊断出患有SCr(I-2;II-1、3、4;III-1、2、3、4)。此外,一名女性(III-8)患有双侧乳腺癌,两人(先证者:IV-1和她父亲的堂妹:III-10)患有慢性胃炎。对先证者、她父亲的堂妹、他的妹妹(III-11)和先证者的妹妹(IV-2)进行了临床和细胞遗传学检查(采用中期法对血淋巴细胞进行染色体21(p12-pter)的G显带,基于染色体不稳定性,100%的细胞进行检测;此外,在4%的细胞中发现染色体2的复杂易位,在2%的细胞中发现染色体21的q臂增加。先证者的妹妹(IV-2)有3%的细胞出现多倍体,1%的细胞出现1号染色体缺失(p34-pter),4%的细胞出现7号染色体缺失(p21-pter)。对先证者的叔叔(III-10)进行了3次细胞遗传学检查,发现先证者的情况,2%的细胞出现核内有丝分裂,2%的细胞出现多倍体,4%的细胞出现超二倍体。他的妹妹(III-11)有4%的细胞出现核内有丝分裂,3%的细胞出现染色体和染色单体断裂,100%的细胞出现染色体21的p臂增加,2%的细胞出现7p缺失。本文讨论了该家族成员中染色体21的现象性质和易位情况。细胞遗传学检查目前正在进行中。

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