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Localized malignant pleural mesothelioma arising in the interlobar fissure: a unique surgical case masquerading clinicopathologically as primary lung adenocarcinoma

机译:小叶间裂引起的局部恶性胸膜间皮瘤:在临床病理上伪装成原发性肺腺癌的独特外科病例

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摘要

An 80-year-old male with previous workplace exposure to asbestos presented with a history of an increase in the pulmonary-to-hilar mass, measuring more than 50 mm in diameter, likely in the right lower lobe. We first interpreted it as suspicious of primary lung adenocarcinoma with direct invasion to the right hilar lymph node. A right middle and lower lobectomy with partial resection of upper lobe was performed, and gross examination showed a hilar tumor lesion, involving the middle/lower lobe to hilar lymph node and looking whitish to yellow-grayish, partly adjacent to the right pulmonary artery. On microscopic examination, the tumor was located on the extrapulmonary, interlobar pleural fissure, predominantly composed of a proliferation of atypical epithelioid cells, often arranged in an irregular and fused tubular growth pattern with an involvement of pulmonary artery. Immunohistochemically, these atypical cells are positive for several mesothelial markers, including calretinin, cytokeratin 5/6, and WT-1, whereas negative for thyroid transcription factor 1. Furthermore, p16 deletions were specifically detected by fluorescence in situ hybridization, and electron microscopy showed numerous, significantly elongated microvilli. Taken together, we finally made a diagnosis of localized malignant pleural mesothelioma, epithelioid-type, arising in the right interlobar fissure between lower and middle lobes. We should be aware that, owing to its characteristic features, clinicians and pathologists might be able to raise interlobar fissure localized malignant pleural mesothelioma as one of the differential diagnoses, based on careful clinicopathological examinations.
机译:一名80岁的男性,以前在工作场所接触过石棉,其肺-肺门肿块有增加的历史,直径超过50mm,可能在右下叶。我们首先将其解释为可疑为原发性肺腺癌,并直接侵犯右肺门淋巴结。右上,下肺叶切除术,上叶部分切除,大体检查显示肺门肿瘤病变,累及中/下叶至肺门淋巴结,外观发白至黄灰色,部分邻近右肺动脉。在显微镜下检查,肿瘤位于肺外叶间胸膜裂隙中,主要由非典型上皮样细胞的增殖组成,通常以不规则且融合的肾小管生长模式排列,并累及肺动脉。免疫组织化学分析,这些非典型细胞对几种间皮标志物呈阳性,包括钙调蛋白,细胞角蛋白5/6和WT-1,而对甲状腺转录因子1呈阴性。此外,通过荧光原位杂交特异性检测到p16缺失,并且电子显微镜显示大量明显伸长的微绒毛。综上所述,我们最终诊断出局部恶性胸膜间皮瘤(上皮样类型),发生在右下叶和中叶之间的叶间裂。我们应该意识到,由于其特征,临床医生和病理学家在仔细的临床病理检查的基础上,可能会提出将叶间裂局部恶性胸膜间皮瘤作为鉴别诊断之一。

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