首页> 外文期刊>Cytopathology >Fine needle aspiration cytology in the work-up of mammographic and ultrasonographic findings in breast cancer screening: an attempt at differentiating in situ and invasive carcinoma.
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Fine needle aspiration cytology in the work-up of mammographic and ultrasonographic findings in breast cancer screening: an attempt at differentiating in situ and invasive carcinoma.

机译:细针穿刺细胞学检查在乳腺癌筛查的钼靶和超声检查结果中的作用:尝试区分原位癌和浸润癌。

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This study evaluated the results of fine needle aspiration cytology (FNAC) from the first four years of organized mammography screening for breast cancer in Oslo, particularly our policy in differentiating in situ and invasive carcinoma. Lesions were aspirated directly, ultrasound guided, by stereotaxic device or biopsy localization plate. All lesions were aspirated by cytopathologists working with the radiologists at the breast diagnostic centre. Smears were evaluated immediately for assessment of adequacy and a preliminary diagnosis was given to the surgeon. When FNAC revealed malignancy, diagnostic terms were as follows: (1) invasive carcinoma; (2) ductal carcinoma in situ of comedo type (high nuclear grade), cannot evaluate infiltration; (3) ductal carcinoma in situ of low nuclear grade and (4) papillary tumour, cannot evaluate infiltration. There were 953 cases, 70% of which were nonpalpable. Insufficient material was obtained in 5.8%. Absolute and complete sensitivity were 81% and 91%, respectively. Specificity was 85%. There were 448 histologically proven carcinomas. 383 of these were invasive. 362 carcinomas (in situ and invasive) (80.8%) were diagnosed directly on FNAC. Distinction between invasive and in situ carcinoma was possible in 294 of 320 directly diagnosed invasive carcinomas (91.8%). PPV of a diagnosis of invasive carcinoma was 97%. Our data showed that definitive cytological diagnosis of invasive carcinoma was possible in more than 90% of fully diagnostic smears and allowed definitive primary surgery in these women.
机译:这项研究评估了在奥斯陆组织的乳房X线摄影筛查的头四年中细针穿刺细胞学检查(FNAC)的结果,特别是我们区分原位癌和浸润癌的政策。通过立体定位仪或活检定位板直接在超声引导下抽吸病变。所有病变均由细胞病理学家与乳腺诊断中心的放射科医生一起抽吸。立即对涂片进行评估,以评估其是否充分,并对外科医生进行初步诊断。当FNAC显示恶性肿瘤时,诊断条件如下:(1)浸润性癌; (2)粉刺型(高核级)导管癌,不能评估浸润; (3)低核级原位导管癌和(4)乳头状肿瘤,不能评估浸润。有953例,其中70%不可触及。得到的材料不足,为5.8%。绝对灵敏度和完全灵敏度分别为81%和91%。特异性为85%。有448个经组织学证实的癌。其中383例是侵入性的。直接在FNAC上诊断出362例癌(原位和浸润性)(80.8%)。在直接诊断的320例浸润癌中,有294例可分为浸润癌和原位癌(91.8%)。诊断为浸润癌的PPV为97%。我们的数据表明,在超过90%的完全诊断涂片中,可以对浸润性癌进行明确的细胞学诊断,并且可以对这些女性进行明确的初次手术。

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