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中国家族性腺瘤性息肉病的临床特征及其永生淋巴细胞系的建立。

Clinical features of familial adenomas polyps in Chinese and establishment of its immortal lymphocyte cell lines.

作者信息

Cai Shan-Rong, Zhang Su-Zhang, Zheng Shu

机构信息

Cancer Institute, 2nd Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, Zhejiang Province, China.

出版信息

World J Gastroenterol. 2007 May 28;13(20):2858-61. doi: 10.3748/wjg.v13.i20.2858.

Abstract

AIM

To reserve the rare Chinese familial adenomas polyp (FAP) family resource and to investigate the clinical features of FAP in Chinese for its diagnosis.

METHODS

Clinical features of patients with FAP were investigated. If there is any question, their medical records were verified. Blood sample was taken and lymphocyte immortal cell lines were established with modified EB-transformation methods. Congenital hypertrophy of retinal pigment epithelium (CHRPE) was checked by an experienced ophthalmologist.

RESULTS

Twenty seven families including 21 classical FAP (CFAP) families, 3 attenuated FAP (AFAP) families, and 3 suspected AFAP families were investigated. A total of 116 lymphocyte immortal cell lines were established from 26 families. In all the FAP families, colorectal cancer occurred at the mean age of 42.84 years. Of the 16 families checked, 15 (93.75%) had CHRPE. The mean number of patients suffering from colorectal neoplasm was 3.14 in CFAP families and 2.0 in AFAP families (P<0.01). The mean oldest age at diagnosis of FAP was 41.75 years in CFAP families, and 58.67 years in AFAP families, respectively (P<0.01). Mean age of development of colorectal cancer was 42.23 in CFAP and 57.33 years old in AFAP (P<0.01). Mean of the earliest age at diagnosis of FAP was 29.95 years in the FAP families with a positive family history and 46.80 years in the FAP families with a negative family history (P < 0.01). The ratio of extra-intestinal tumors to colorectal neoplasms was different in the two kinds of families with positive and negative family history (P<0.01).

CONCLUSION

Additional use of ciclosporin will effectively improve to establish lymphocyte immortal cell lines with modified EB- transformation methods. In Chinese FAP, there was a high frequency of CHRPE , and a later age at diagnosis and a later age of development of colorectal cancer in AFAP. And earlier age at diagnosis in FAP with positive family history was also found that will help to diagnose various kinds of FAP in Chinese.

摘要

目的

保存罕见的中国家族性腺瘤性息肉病(FAP)家系资源,并研究中国FAP的临床特征以助于其诊断。

方法

对FAP患者的临床特征进行调查。如有疑问,核实其病历。采集血样,采用改良的EB转化方法建立淋巴细胞永生化细胞系。由经验丰富的眼科医生检查视网膜色素上皮先天性肥大(CHRPE)情况。

结果

共调查了27个家系,其中包括21个经典FAP(CFAP)家系、3个 attenuated FAP(AFAP)家系和3个疑似AFAP家系。从26个家系中建立了116个淋巴细胞永生化细胞系。在所有FAP家系中,结直肠癌发病的平均年龄为42.84岁。在接受检查的16个家系中,15个(93.75%)有CHRPE。CFAP家系中患结直肠肿瘤的患者平均人数为3.14人,AFAP家系为2.0人(P<0.01)。CFAP家系中FAP诊断时的平均最高年龄为41.75岁,AFAP家系为58.67岁(P<0.01)。CFAP家系中结直肠癌发病的平均年龄为42.23岁,AFAP家系为57.33岁(P<0.01)。有家族史的FAP家系中FAP诊断的最早平均年龄为29.95岁,无家族史的FAP家系为46.80岁(P<0.01)。有家族史和无家族史的两类家系中肠外肿瘤与结直肠肿瘤的比例不同(P<0.01)。

结论

额外使用环孢素将有效提高采用改良EB转化方法建立淋巴细胞永生化细胞系的成功率。在中国FAP中,CHRPE的发生率较高,AFAP的诊断年龄和结直肠癌发病年龄较晚。还发现有家族史的FAP诊断年龄较早,这将有助于诊断中国的各种FAP。

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