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癌症家族综合征中的子宫内膜癌。

Endometrial carcinoma in the cancer family syndrome.

作者信息

Hakala T, Mecklin J P, Forss M, Järvinen H, Lehtovirta P

机构信息

Department of Obstetrics and Gynecology of Helsinki University Central Hospital, Finland.

出版信息

Cancer. 1991 Oct 1;68(7):1656-9. doi: 10.1002/1097-0142(19911001)68:7<1656::aid-cncr2820680732>3.0.co;2-7.

DOI:10.1002/1097-0142(19911001)68:7<1656::aid-cncr2820680732>3.0.co;2-7
PMID:1893367
Abstract

The study group consisted of 26 women with endometrial adenocarcinoma belonging to 19 cancer families. Age at the onset of cancer, the stage and histologic differentiation of the tumor, initial symptoms, other malignancies, 5-year survival, and transmission of cancer to descendants were studied. The focus was on the importance of endometrial carcinoma in the tumor spectrum. The diagnosis of cancer family was delayed in 14 of the 19 families because endometrial carcinoma was not included in the primary diagnostic carcinoma. This delay may have been harmful to 16 family members who had carcinomas later in life. In ten of the 14 women with multiple malignancies, endometrial adenocarcinoma was the primary malignancy diagnosed, thus enabling the suspicion of a gene carrier and screening for subsequent malignancies. The authors concluded that endometrial carcinoma is a significant component of cancer family syndrome and should be included in the main criteria of Lynch syndrome II.

摘要

研究组由来自19个癌症家族的26例子宫内膜腺癌女性组成。对癌症发病年龄、肿瘤分期和组织学分化、初始症状、其他恶性肿瘤、5年生存率以及癌症向后代的传递情况进行了研究。重点在于子宫内膜癌在肿瘤谱中的重要性。19个家族中有14个家族的癌症家族诊断被延迟,原因是原发性诊断癌中未包括子宫内膜癌。这种延迟可能对16名后来患癌的家庭成员有害。在14例患有多种恶性肿瘤的女性中,有10例的原发性恶性肿瘤诊断为子宫内膜腺癌,从而得以怀疑基因携带者并对后续恶性肿瘤进行筛查。作者得出结论,子宫内膜癌是癌症家族综合征的重要组成部分,应纳入林奇综合征II的主要标准。

相似文献

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Endometrial carcinoma in the cancer family syndrome.癌症家族综合征中的子宫内膜癌。
Cancer. 1991 Oct 1;68(7):1656-9. doi: 10.1002/1097-0142(19911001)68:7<1656::aid-cncr2820680732>3.0.co;2-7.
2
Uterine Mesenchymal Tumors: Hereditary Aspects.子宫间质肿瘤:遗传方面。
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Endometrial adenocarcinoma: genetic analysis suggesting heritable site-specific uterine cancer.子宫内膜腺癌:遗传分析提示遗传性位点特异性子宫癌
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Genetic testing by cancer site: uterus.按癌症部位进行的基因检测:子宫。
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Cancer family syndrome of Lynch.林奇癌症家族综合征
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Other Gynecologic Cancers: endometrial, ovarian, vulvar and vaginal cancers.其他妇科癌症:子宫内膜癌、卵巢癌、外阴癌和阴道癌。
BMC Womens Health. 2004 Aug 25;4 Suppl 1(Suppl 1):S14. doi: 10.1186/1472-6874-4-S1-S14.
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Clinical features and mismatch repair gene mutation screening in Chinese patients with hereditary nonpolyposis colorectal carcinoma.中国遗传性非息肉病性结直肠癌患者的临床特征及错配修复基因突变筛查
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Genetic implications of double primary cancers of the colorectum and endometrium.结直肠癌和子宫内膜癌双原发性癌症的遗传学意义。
J Med Genet. 1998 Dec;35(12):978-84. doi: 10.1136/jmg.35.12.978.
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Linkage of a major breast cancer gene to chromosome 17q12-21: results from 15 Edinburgh families.一种主要乳腺癌基因与17号染色体q12 - 21区域的连锁关系:来自15个爱丁堡家族的研究结果
Am J Hum Genet. 1993 Apr;52(4):723-9.
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Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage.2号染色体和3号染色体上的错配修复基因在可通过连锁分析评估的遗传性非息肉病性结直肠癌家族中占很大比例。
Am J Hum Genet. 1994 Oct;55(4):659-65.