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细胞块免疫细胞化学对胸腔积液的精细诊断。

Refined Diagnosis of Pleural Effusions by Immunocytochemistry of Cell Blocks.

机构信息

Department of Respiratory Medicine, Gävle Hospital, Gävle, Sweden;

Department of Oncology-Pathology, Karolinska Biomics Center, Karolinska Institute, Stockholm, Sweden.

出版信息

Anticancer Res. 2023 Feb;43(2):669-673. doi: 10.21873/anticanres.16204.

Abstract

BACKGROUND/AIM: The main objective of microscopic examination of pleural effusions is to ascertain the presence of malignant cells. Effusions prepared routinely using May-Grünwald-Giemsa (MGG)- and Papanicolaou (PAP)-staining can, in a number of cases, provide inconclusive cytological results regarding malignancy.

PATIENTS AND METHODS

This report describes the refined diagnosis of such cases based on immunocytochemical analysis of pleural effusion cell blocks. Of the 340 pleural effusions obtained during 2019 at the Department of Clinical Cytology, Gävle Hospital, Sweden, 63 (18.5%) contained atypical cells of undetermined significance or potentially malignant cells.

RESULTS

This diagnosis could be refined using Epithelial Cell Adhesion Molecule/EPCAM (BEREP4) immunocytochemical analysis of effusion cell blocks, allowing previously inconclusive effusions to be classified as clearly benign 42/63 (66.7%) or malignant 21/63 (33.3%). Effusions initially diagnosed as clearly malignant (27/340; 7.9%) were all 27 (100%) BEREP4-immuno-stained. Most BEREP4-positive effusions (37/48; 77.1%) were also carcinoembryonic antigen (CEA) positive. The number of BEREP4-positive cells, however, tended to exceed that of CEA-positive cells. The BEREP4 positive effusions were further examined using different monoclonal antibodies, such as Thyroid transcription factor 1 (TTF-1) for primary pulmonary adenocarcinoma, to determine the original site of the primary tumour.

CONCLUSION

Immunohistochemical staining of pleural effusion cell blocks significantly refines the diagnosis of serous pleural effusions, especially in cases where the preliminary diagnosis was atypical cells of undetermined significance or potentially malignant cells. Furthermore, in the cases of malignancy, the origin of the primary tumour could most often be determined.

摘要

背景/目的:胸腔积液的显微镜检查的主要目的是确定恶性细胞的存在。使用迈-格-吉(May-Grünwald-Giemsa,MGG)-和巴氏(Papanicolaou,PAP)染色常规制备的积液在许多情况下,关于恶性肿瘤的细胞学结果可能无法得出明确结论。

患者和方法

本报告描述了基于胸腔积液细胞块免疫细胞化学分析对这些病例进行的精细诊断。在瑞典加夫勒医院临床细胞学系 2019 年获得的 340 例胸腔积液中,有 63 例(18.5%)含有意义未明的非典型细胞或潜在恶性细胞。

结果

使用上皮细胞黏附分子/上皮细胞钙黏蛋白(Epithelial Cell Adhesion Molecule/EPCAM,BEREP4)免疫细胞化学分析胸腔积液细胞块,可以对以前不确定的积液进行分类,明确良性 42/63(66.7%)或恶性 21/63(33.3%)。最初诊断为明确恶性的积液(27/340;7.9%)均为 27 例(100%)BEREP4 免疫染色阳性。大多数 BEREP4 阳性积液(37/48;77.1%)也为癌胚抗原(carcinoembryonic antigen,CEA)阳性。然而,BEREP4 阳性细胞的数量往往超过 CEA 阳性细胞的数量。进一步使用不同的单克隆抗体,如甲状腺转录因子 1(Thyroid transcription factor 1,TTF-1),对 BEREP4 阳性积液进行检查,以确定原发性肿瘤的原始部位。

结论

胸腔积液细胞块的免疫组织化学染色显著细化了浆膜腔积液的诊断,尤其是在初步诊断为意义未明的非典型细胞或潜在恶性细胞的情况下。此外,在恶性肿瘤的情况下,通常可以确定原发性肿瘤的起源。

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