Marcus J N, Watson P, Page D L, Lynch H T
Department of Pathology, Creighton University, Omaha, Neb.
J Natl Cancer Inst Monogr. 1994(16):23-34.
The pathology of early-age onset breast cancer is considered here from three perspectives: 1) benign proliferative disease, 2) the cancers themselves, and 3) familial and hereditary breast cancer. Hereditary breast cancer, a subset of familial breast cancer featuring a strong autosomal dominant pedigree pattern and multiple primary cancers, has a strong predilection for younger women, accounting for about one half of breast cancers under age 30. With respect to benign proliferative disease, the increased relative risk of breast cancer associated with proliferative disease with atypia, about fourfold to fivefold for all ages, is doubled by the presence of a family history of breast cancer and amplified by young age. With respect to the carcinomas, the relative incidences of medullary carcinoma and ductal carcinoma in situ are increased in young women, while lobular and tubular carcinomas are decreased. Invasive breast cancer is higher grade and more proliferative in younger women, as measured by thymidine-labeling index, DNA flow cytometric S-phase fraction, and proliferation-associated proteins. The increased fraction of ductal carcinoma in situ and higher grade invasive cancers may help to account, respectively, for increased recurrence rates with conservative therapy, and more aggressive natural history in younger women. Familial breast cancers show trends for increased medullary type, but the effect is not independent of age. Weak associations of family history with tubular carcinoma have been reported, but data for associations with lobular carcinoma in situ and invasive lobular carcinoma are conflicting. Hereditary breast cancer as a class has higher tumor proliferation rates, an effect independent of age. Knowledge of the pathology and biomarker characteristics of BRCA1 gene-linked hereditary breast cancers, which account for a substantial fraction of breast cancers in younger women, should shed light on the nature of the responsible gene(s) and guide approaches to therapy and prophylaxis.
1)良性增生性疾病;2)癌症本身;3)家族性和遗传性乳腺癌。遗传性乳腺癌是家族性乳腺癌的一个子集,具有强烈的常染色体显性谱系模式和多原发性癌症,对年轻女性有很强的偏好,占30岁以下乳腺癌的一半左右。关于良性增生性疾病,伴有异型增生的增生性疾病相关的乳腺癌相对风险增加,所有年龄段约为4至5倍,有乳腺癌家族史会使其增加一倍,且在年轻时风险会进一步放大。关于癌症,年轻女性中髓样癌和导管原位癌的相对发病率增加,而小叶癌和管状癌的发病率降低。通过胸腺嘧啶标记指数、DNA流式细胞术S期分数和增殖相关蛋白测量,年轻女性的浸润性乳腺癌分级更高且增殖性更强。导管原位癌比例增加和浸润性癌症分级更高,可能分别有助于解释保守治疗后复发率增加以及年轻女性更具侵袭性的自然病程。家族性乳腺癌有髓样类型增加的趋势,但这种影响并非独立于年龄。有报道称家族史与管状癌的关联较弱,但关于与小叶原位癌和浸润性小叶癌关联的数据相互矛盾。作为一个类别,遗传性乳腺癌具有更高的肿瘤增殖率,这一影响与年龄无关。了解BRCA1基因相关遗传性乳腺癌的病理学和生物标志物特征,这些特征在年轻女性乳腺癌中占很大比例,应该能够阐明致病基因的性质,并指导治疗和预防方法。