Yabuuchi Yuki, Hiroshima Kenzo, Oshima Hisayuki, Kanazawa Jun, Hayashihara Kenji, Nakagawa Takayuki, Shimanouchi Masaki, Usui Shingo, Oh-Ishi Shuji, Saito Takefumi, Hizawa Nobuyuki, Minami Yuko
Department of Respiratory Medicine, National Hospital Organization, Ibaraki Higashi National Hospital, Tokai-mura, Ibaraki 319-1113, Japan.
Department of Pulmonary Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki 305-8576, Japan.
Oncol Lett. 2022 Oct 25;24(6):440. doi: 10.3892/ol.2022.13560. eCollection 2022 Dec.
Mesothelioma (MIS) is defined as a preinvasive mesothelioma that forms a single layer of mild atypical mesothelial cells lining on the serosa surface of pleura. The atypical mesothelial cells present loss of BRCA-1 associated protein-1 (BAP-1) and/or methylthioadenosine phosphorylase as examined by immunohistochemistry (IHC) and/or homozygous deletion of cyclin-dependent kinase inhibitor 2A/p16 as examined by fluorescence hybridization. It is difficult to diagnose because of the unremarkable clinical findings except for pleural effusion. The present report describes a case in which MIS was diagnosed at the time of sampling due to the presence of clearly malignant mesothelial cells in the pleural fluid. In 2016, a 74-year-old man with a history of past exposure to asbestos was admitted to Ibaraki Higashi National Hospital (Tokai-mura, Japan) with dyspnea. Chest CT indicated only right pleural effusion. Malignant mesothelial cells were suspected in a cell block made using pleural effusion; therefore, right pleural biopsy was performed. Pathologically, there was proliferation of mesothelial cells with mild atypia that formed a single-flat layer on the pleural surface; however, there was no invasion. Furthermore, IHC revealed loss of BAP-1 in cells from the biopsied pleura and pleural effusion. MIS was suspected at the time; however, the patient arbitrarily quit his medical check-ups. After 44 months, the patient was readmitted to our hospital complaining of dyspnea. CT indicated a large right pleural mass. A specimen of the mass obtained via CT-guided needle biopsy revealed malignant mesothelioma. The patient continued to deteriorate and eventually died. This case indicated that pleural effusion could be used to demonstrate overtly malignant mesothelial cells and diagnose MIS at the time of sampling. To the best of our knowledge, this is first report of MIS with overtly malignant mesothelial cells in pleural effusion. Pleural effusion may serve an important role in MIS diagnosis.
间皮瘤(MIS)被定义为一种侵袭前的间皮瘤,它在胸膜浆膜表面形成单层轻度非典型间皮细胞。通过免疫组织化学(IHC)检测,非典型间皮细胞表现为BRCA-1相关蛋白-1(BAP-1)缺失和/或甲硫腺苷磷酸化酶缺失,和/或通过荧光杂交检测发现细胞周期蛋白依赖性激酶抑制剂2A/p16纯合缺失。除了胸腔积液外,由于临床症状不明显,所以很难诊断。本报告描述了一例因胸腔积液中存在明显恶性间皮细胞而在采样时被诊断为MIS的病例。2016年,一名有石棉接触史的74岁男性因呼吸困难入住茨城东部国立医院(日本东海村)。胸部CT仅显示右侧胸腔积液。在使用胸腔积液制作的细胞块中怀疑有恶性间皮细胞;因此,进行了右侧胸膜活检。病理检查显示,间皮细胞增生,有轻度异型性,在胸膜表面形成单层扁平层;然而,没有侵袭。此外,免疫组织化学显示活检胸膜和胸腔积液中的细胞BAP-1缺失。当时怀疑是MIS;然而,患者擅自停止了体检。44个月后,患者因呼吸困难再次入住我院。CT显示右侧胸腔有一个大肿块。通过CT引导下针吸活检获得的肿块标本显示为恶性间皮瘤。患者病情持续恶化,最终死亡。该病例表明,胸腔积液可用于显示明显的恶性间皮细胞,并在采样时诊断MIS。据我们所知,这是第一例胸腔积液中有明显恶性间皮细胞的MIS报告。胸腔积液可能在MIS诊断中起重要作用。