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淋巴结转移细针细胞学检查的全面诊断方法路线图。

A roadmap for a comprehensive diagnostic approach to fine needle cytology of lymph node metastases.

机构信息

Department of Public Health, University of Naples "Federico II", Naples, Italy.

Hematology Section, Department of Clinical Medicine and Surgery, University of Naples "Federico II", Naples, Italy.

出版信息

Cytopathology. 2022 Nov;33(6):668-677. doi: 10.1111/cyt.13172. Epub 2022 Sep 5.

DOI:10.1111/cyt.13172
PMID:35986701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9826057/
Abstract

OBJECTIVE

Fine needle cytology (FNC) is widely used as a first-line procedure in the diagnostic algorithm of lymphadenopathies. In a metastatic setting, a first-line diagnostic approach identifies non-haematopoietic malignancy; however, cytopathologists could also provide a second diagnostic level, identifying the origin of the primary tumour. This paper outlines a comprehensive and practical approach to the cytological diagnosis of lymph node metastases.

METHODS

Cytological diagnoses of lymph node metastases performed over a 10-year period were selected and divided into two groups. The first group, labelled "oncological," comprised patients with a previous history of malignancy; the second group, labelled "naïve," included patients with no relevant history. Pathology records were retrieved to record microscopic findings, namely, background appearance, group architecture, and specific cell features; data from cell block (CB) preparations were also collected.

RESULTS

Overall, 982 cases were selected: 497 cases (50.61%) in the naïve group, and 485 (49.39%) in the oncological group. Overall, a second diagnostic level was achieved in 834/982 cases (84.92%); cases diagnosed as carcinoma not otherwise specified were more frequent in the naïve group than in the oncological group (17.51% vs. 8.04%, P < 0.01). Notably, although CB material was available in only 44.87% of the naïve cases, we were able to achieve a second diagnostic level thanks to the integration of clinical and cytomorphological findings, plus lymph node topography, in 82.49% of the cases.

CONCLUSION

Our results confirmed that in a metastatic setting, FNC can reliably lead to the identification of the origin of the primary tumour.

摘要

目的

细针细胞学(FNC)广泛用作淋巴结病诊断算法的一线程序。在转移性疾病中,一线诊断方法可识别非造血恶性肿瘤;然而,细胞病理学家也可以提供第二个诊断级别,确定原发性肿瘤的起源。本文概述了一种全面实用的方法,用于诊断淋巴结转移的细胞学。

方法

选择了在过去 10 年中进行的淋巴结转移的细胞学诊断,并将其分为两组。第一组,标记为“肿瘤学”,包括有恶性肿瘤病史的患者;第二组,标记为“幼稚”,包括没有相关病史的患者。检索病理记录以记录显微镜检查结果,即背景外观、组结构和特定细胞特征;还收集了细胞块(CB)制备的数据。

结果

共选择了 982 例病例:幼稚组 497 例(50.61%),肿瘤组 485 例(49.39%)。总体而言,834/982 例(84.92%)达到了二级诊断水平;幼稚组中诊断为非特指癌的病例比肿瘤组更常见(17.51%比 8.04%,P < 0.01)。值得注意的是,尽管只有 44.87%的幼稚病例有 CB 材料,但由于整合了临床和细胞学发现,加上淋巴结解剖结构,我们能够在 82.49%的病例中达到二级诊断水平。

结论

我们的结果证实,在转移性疾病中,FNC 可以可靠地确定原发性肿瘤的起源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a3/9826057/382db9f69f25/CYT-33-668-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a3/9826057/0c2fd0cabe01/CYT-33-668-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a3/9826057/4ff57289a16a/CYT-33-668-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a3/9826057/396a00047bd5/CYT-33-668-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a3/9826057/2792ee8c9dd7/CYT-33-668-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a3/9826057/382db9f69f25/CYT-33-668-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a3/9826057/0c2fd0cabe01/CYT-33-668-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a3/9826057/4ff57289a16a/CYT-33-668-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a3/9826057/396a00047bd5/CYT-33-668-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a3/9826057/2792ee8c9dd7/CYT-33-668-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a3/9826057/382db9f69f25/CYT-33-668-g001.jpg

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