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胸膜原发性上皮样肉瘤 1 例报告。

A Case of Primary Epithelioid Sarcoma of the Pleura.

机构信息

Department of General Thoracic and Breast Surgery, Iwata City Hospital, Iwata, Shizuoka, Japan.

出版信息

Am J Case Rep. 2023 Jan 4;24:e938696. doi: 10.12659/AJCR.938696.

DOI:10.12659/AJCR.938696
PMID:36597286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9827392/
Abstract

BACKGROUND Epithelioid sarcoma is a rare tumor and that is extremely rare as a primary pleural neoplasm. On imaging, it may appear similar to malignant pleural mesothelioma; thus, it can be difficult to diagnose. CASE REPORT A 64-year-old Asian woman, who had a treatment history of cervix adenocarcinoma, was admitted with dyspnea and right massive pleural effusion. Chest drainage was performed, and malignant cells were found in the pleural effusion. The malignant cells were thought to be metastasized from previous cervical cancer. We continued pleural drainage; however, the volume of the pleural effusion did not decrease. On the 5th hospital day, the chest tube became occluded. Computed tomography showed structures similar to empyema. Pleural irrigation and fibrinolytic therapy did not improve her condition. Empyema curettage was performed on the 14th hospital day. The resected pleura was submitted for pathological examination and showed tumor lesion but not metastatic adenocarcinoma of the cervix. The intrathoracic tumor grew extremely rapidly, and the patient died of respiratory failure on postoperative day 8 (22nd hospital day) before a diagnosis could be made. The final pathological diagnosis obtained on the 34th hospital day was epithelioid sarcoma. CONCLUSIONS For patients who appear to have empyema complicated by neoplastic lesions, a histopathological examination should also be performed to ensure accurate diagnosis. In addition, if a tumorous lesion is detected and it is neither metastatic nor malignant pleural mesothelioma, pleural epithelioid sarcoma should be added to the differential diagnosis in the presence of a rapidly growing and histologically difficult-to-diagnose pleural tumor.

摘要

背景

上皮样肉瘤是一种罕见的肿瘤,作为原发性胸膜肿瘤极其罕见。在影像学上,它可能与恶性胸膜间皮瘤相似,因此诊断较为困难。

病例报告

一名 64 岁亚裔女性,曾患有宫颈癌腺癌,因呼吸困难和右侧大量胸腔积液入院。行胸腔引流,胸腔积液中发现恶性细胞。这些恶性细胞被认为是来自先前宫颈癌的转移。我们继续进行胸腔引流,但胸腔积液量没有减少。在第 5 天,胸管堵塞。胸部 CT 显示类似脓胸的结构。胸腔灌洗和纤维蛋白溶解治疗均未改善她的病情。第 14 天进行脓胸清创术。切除的胸膜送检病理检查,显示肿瘤病变,但未发现宫颈转移性腺癌。胸腔内肿瘤生长极为迅速,患者在术后第 8 天(第 22 天)因呼吸衰竭死亡,在明确诊断之前。第 34 天的最终病理诊断为上皮样肉瘤。

结论

对于疑似伴有肿瘤病变的脓胸患者,也应进行组织病理学检查以确保准确诊断。此外,如果发现肿瘤病变,既不是转移性病变,也不是恶性胸膜间皮瘤,在存在快速生长且组织学诊断困难的胸膜肿瘤时,应将胸膜上皮样肉瘤纳入鉴别诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bae0/9827392/e4fa23bb0dad/amjcaserep-24-e938696-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bae0/9827392/7b0b267a585f/amjcaserep-24-e938696-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bae0/9827392/e4fa23bb0dad/amjcaserep-24-e938696-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bae0/9827392/7b0b267a585f/amjcaserep-24-e938696-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bae0/9827392/e4fa23bb0dad/amjcaserep-24-e938696-g002.jpg

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