Jimenez R E, Visscher D W
Department of Pathology, Harper Hospital, the Karmanos Cancer Institute, and Wayne State University, Detroit, MI 48201, USA.
Hum Pathol. 1998 Dec;29(12):1412-9. doi: 10.1016/s0046-8177(98)90009-0.
Breast biopsy or mastectomy cases having diagnoses of carcinoma in situ with "microinvasion," "minimal invasion," "focal invasion," or "suggestive of invasion" were reviewed and all histologically identified foci of invasive disease from each case were measured using an ocular micrometer. Cases in which any single focus of invasion was greater than 5 mm or the added size of separate invasive foci exceeded 10 mm were excluded, resulting in a study group of 75 patients. Invasive neoplasm was present in the initial biopsy in 69 of 75 cases (92%); however, residual invasive neoplasm was found in the subsequent lumpectomy/mastectomy from 14 of these (20%). In 59% of cases, two or more histologically separate foci of invasion were identified. Invasive foci consisted of isolated cells or cell clusters, each less than 1 mm (microfocal invasion), in 33% of cases. In 12 cases, the sum of individual invasive foci was 5 to 10 mm. Axillary lymph nodes (LN) from 5 of 69 patients (7%) contained metastatic carcinoma (four cases, one LN positive; one case, two LN positive). The cumulative sizes of all invasive foci in the LN-positive group were microfocal invasion (one case), 0.6 mm (one case), 1.1 mm, 2.5 mm, and 5.8 mm. The difference in frequency of axillary node metastasis between tumors with microfocal and measurable invasion (4.3% v 8.6%) was not statistically significant. Follow-up data were available on 55 cases (mean interval, 66.1 months). One (node-negative) patient had duct carcinoma in situ recurrence in the same breast 4 years after initial treatment. Another (with unknown node status) developed an axillary lymph node metastasis 13 months after initial treatment (96% disease-free survival). We conclude that microscopic stromal invasion in breast carcinoma, at least in the setting of significant in situ component, is often initiated from multiple foci. Patients with microscopically invasive breast carcinoma have a small but significant risk of axillary metastases, although a highly favorable survival.
对诊断为原位癌伴“微浸润”“最小浸润”“局灶浸润”或“提示浸润”的乳房活检或乳房切除术病例进行回顾,并使用目镜测微计测量每个病例中所有经组织学鉴定的浸润性病变灶。任何单个浸润灶大于5mm或多个独立浸润灶的总大小超过10mm的病例被排除,最终形成了一个由75例患者组成的研究组。75例病例中有69例(92%)在初次活检时就存在浸润性肿瘤;然而,在随后的肿块切除术/乳房切除术中,其中14例(20%)发现了残留的浸润性肿瘤。59%的病例中发现了两个或更多组织学上独立的浸润灶。33%的病例中,浸润灶由孤立的细胞或细胞簇组成,每个小于1mm(微灶浸润)。12例病例中,单个浸润灶的总和为5至10mm。69例患者中有5例(7%)的腋窝淋巴结(LN)含有转移性癌(4例,1个LN阳性;1例,2个LN阳性)。LN阳性组中所有浸润灶的累积大小分别为微灶浸润(1例),0.6mm(1例),1.1mm,2.5mm和5.8mm。微灶浸润和可测量浸润的肿瘤之间腋窝淋巴结转移频率的差异(4.3%对8.6%)无统计学意义。55例病例有随访数据(平均间隔66.1个月)。1例(淋巴结阴性)患者在初次治疗4年后同侧乳房出现原位导管癌复发。另1例(淋巴结状态未知)在初次治疗13个月后发生腋窝淋巴结转移(无病生存率96%)。我们得出结论,乳腺癌的微小间质浸润,至少在原位成分占主导的情况下,通常由多个病灶起始。显微镜下浸润性乳腺癌患者发生腋窝转移的风险虽小但显著,尽管生存率很高。