Localized malignant pleural mesothelioma arising in the interlobar fissure: a unique surgical case masquerading clinicopathologically as primary lung adenocarcinoma
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- Xin Guo
- Department of Pathology and Laboratory Medicine, Kanazawa Medical University, Uchinada, Japan
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- Jiro Watanabe
- Laboratory of Pathology, National Hospital Organization Fukuyama Medical Center, Fukuyama, Japan
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- Kenji Takahashi
- Department of Thoracic Surgery, National Hospital Organization Fukuyama Medical Center, Fukuyama, Japan
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- Tatsuro Hayashi
- Department of Thoracic Surgery, National Hospital Organization Fukuyama Medical Center, Fukuyama, Japan
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- Nozomu Kurose
- Laboratory of Pathology, National Hospital Organization Fukuyama Medical Center, Fukuyama, Japan
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- Yasuyuki Sasaguri
- Laboratory of Pathology, National Hospital Organization Fukuyama Medical Center, Fukuyama, Japan
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- Hidetaka Uramoto
- Department of Thoracic Surgery, Kanazawa Medical University, Uchinada, Japan
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- Hiromi Iwagaki
- Department of Surgery, National Hospital Organization Fukuyama Medical Center, Fukuyama, Japan
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- Kazuki Nabeshima
- Department of Pathology, Fukuoka University School of Medicine and Hospital, Fukuoka, Japan
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- Sohsuke Yamada
- Department of Pathology and Laboratory Medicine, Kanazawa Medical University, Uchinada, Japan
書誌事項
- 公開日
- 2019-01
- 権利情報
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- https://journals.sagepub.com/page/policies/text-and-data-mining-license
- DOI
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- 10.1177/2050313x18824802
- 公開者
- SAGE Publications
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説明
<jats:p> 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. </jats:p>
収録刊行物
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- SAGE Open Medical Case Reports
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SAGE Open Medical Case Reports 7 2019-01
SAGE Publications