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Invasive cribriform carcinoma of the breast: a clinicopathological analysis of 12 cases with review of literature

机译:乳腺浸润型筛状癌:12例临床病理分析并文献复习

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摘要

Invasive cribriform carcinoma (ICC) is a rare type of invasive breast cancer. We aim to investigate the clinicopathological features, immunophenotypes, diagnosis and differential diagnosis of ICC. Thus, clinicopathological data of 12 ICC patients were collected. All 12 cases were female, aged 38 to 75 years, with a median age of 53 years old. The maximum diameter of the tumor was 2 cm to 10 cm, in which the median tumor size was 2.54 cm in pure ICC and classical ICC. Microscopically, the cancer nests of ICC assumed an invasive, irregular island-shaped distribution, with an irregular mesh structure internally and fibrous reactions around most cancer nests. 67% (8/12) of cases were grade 1 and 33% (4/12) of cases were grade 2 tumors. Immunohistochemically, ER and PR were moderately to strongly positive with the positive tumor cell number accounting for 30% to 95% in all cases. HER-2 was negative in all cases except in one case which was positive (2+). Myoepithelial markers such as Calponin, p63, CK5/6 and CD10 were all negative in the cancer nests. 58% (7/12) of cases had a ki67 index of ≤ 14%. All follow-up patients were followed for 12 to 70 months (with a mean of 42 months), and were disease-free after treatment except for one patient whom we lost during the follow up. In conclusion, ICC, as a special type of breast cancer, has its unique clinicopathological and immunophenotypic characteristics, leading to a good prognosis.
机译:侵袭性筛状癌(ICC)是一种罕见的侵袭性乳腺癌。我们旨在调查ICC的临床病理特征,免疫表型,诊断和鉴别诊断。因此,收集了12例ICC患者的临床病理数据。 12例均为女性,年龄38〜75岁,中位年龄53岁。肿瘤的最大直径为2 cm至10 cm,其中在纯ICC和经典ICC中,中位肿瘤大小为2.54 cm。在显微镜下,ICC的癌巢呈侵入性,不规则的岛状分布,内部具有不规则的网状结构,并且大多数癌巢周围均发生纤维反应。 67%(8/12)的患者为1级肿瘤,33%(4/12)的患者为2级肿瘤。免疫组织化学分析,ER和PR为中度至强阳性,阳性细胞数占所有病例的30%至95%。在所有情况下,HER-2均为阴性,但有1例为阳性(2+)。肌钙蛋白,p63,CK5 / 6和CD10等肌上皮标志物在癌巢中均为阴性。 58%(7/12)的患者的ki67指数≤14%。所有随访患者均接受了12到70个月的随访(平均42个月),除一名患者在随访过程中丢失外,其余均无疾病治疗。总之,ICC作为一种特殊类型的乳腺癌,具有独特的临床病理和免疫表型特征,因此预后良好。

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