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恶性间皮瘤积液的细胞遗传学分析。细胞学诊断的辅助手段。

Cytogenetic analysis of effusions from malignant mesothelioma. A diagnostic adjunct to cytology.

作者信息

Granados R, Cibas E S, Fletcher J A

机构信息

Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

Acta Cytol. 1994 Sep-Oct;38(5):711-7.

PMID:8091903
Abstract

Most patients with malignant mesothelioma (MM) present with an effusion, but distinguishing malignant from reactive mesothelial cells by conventional cytology may be difficult. We investigated the possibility of identifying clonal cytogenetic aberrations in pleural or peritoneal fluid from 10 patients with a clinical suspicion of MM. Direct metaphase harvests and short-term cultures were performed on fresh fluid. Clonal cytogenetic aberrations indicative of malignancy, with findings previously reported in association with mesothelioma, were found in all patients; these included del(1p), del(3p) and del(22q). Cytologic examination of the effusions showed malignant cells consistent with MM in 5 patients and atypical mesothelial cells suggestive of MM in 4. In one case the cytology of several samples of pleural fluid was within normal limits. Subsequent histology confirmed the diagnosis of MM in 9 of the 10 patients; medical complications precluded tissue biopsy in the 10th. We conclude that the cytogenetic analysis of effusions may be a useful and reliable adjunct to cytology in the diagnosis of MM.

摘要

大多数恶性间皮瘤(MM)患者会出现积液,但通过传统细胞学方法区分恶性间皮细胞和反应性间皮细胞可能存在困难。我们调查了对10例临床怀疑为MM的患者的胸腔或腹腔积液进行克隆细胞遗传学异常鉴定的可能性。对新鲜积液进行了直接中期收获和短期培养。在所有患者中均发现了提示恶性的克隆细胞遗传学异常,这些异常与先前报道的与间皮瘤相关的发现一致;包括1p缺失、3p缺失和22q缺失。积液的细胞学检查显示,5例患者的恶性细胞与MM一致,4例患者的非典型间皮细胞提示为MM。在1例病例中,多个胸腔积液样本的细胞学检查结果在正常范围内。随后的组织学检查证实10例患者中有9例诊断为MM;第10例患者因医疗并发症未能进行组织活检。我们得出结论,积液的细胞遗传学分析可能是MM诊断中细胞学的一种有用且可靠的辅助手段。

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