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胸膜孤立性纤维瘤:1例巨大恶性肿瘤术后复发的临床病例

Solitary Fibrous Tumor of the Pleura: A Clinical Case of a Giant Malignant Tumor With Post-surgical Recurrence.

作者信息

Razouq Boujemaa, Azal Hamza, Cedric Joel Bayem, Ibba Mouhsin, Fenane Hicham, Msougar Yassine

机构信息

Thoracic Surgery, Mohammed VI University Hospital, Marrakesh, MAR.

出版信息

Cureus. 2025 Feb 7;17(2):e78713. doi: 10.7759/cureus.78713. eCollection 2025 Feb.

DOI:10.7759/cureus.78713
PMID:40065864
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11893203/
Abstract

Solitary fibrous tumor of the pleura (SFTP) is a rare mesenchymal tumor, making up a small fraction of primary pleural tumors. It is typically benign but can display malignant features. This case presents a 59-year-old patient with a giant malignant SFTP located in the right posterior inferior mediastinum, which caused significant compression of adjacent structures, including the lung, heart, and esophagus. The patient initially presented with dyspnea, chest pain, and weight loss. Imaging studies revealed a voluminous mass with heterogeneous characteristics, calcifications, and pleural effusion, while biopsy and histopathological analysis confirmed a mesenchymal proliferation consistent with a solitary fibrous tumor. Despite partial resection, due to the tumor's size and extensive adhesions, complete removal was not feasible. Postoperative histological findings revealed features indicative of malignancy, including a high mitotic index and slight nuclear atypia. The patient declined adjuvant chemotherapy and radiotherapy, and experienced recurrence within four months. Despite the lack of chemosensitivity, the tumor progressed locally, and the patient's clinical condition worsened. This case highlights the challenges in diagnosing and managing malignant SFTPs, emphasizing the importance of individualized treatment plans and the necessity for long-term follow-up due to the risk of recurrence and poor prognosis following incomplete resection.

摘要

胸膜孤立性纤维瘤(SFTP)是一种罕见的间叶组织肿瘤,仅占原发性胸膜肿瘤的一小部分。它通常为良性,但也可表现出恶性特征。该病例为一名59岁患者,患有位于右后下纵隔的巨大恶性SFTP,对包括肺、心脏和食管在内的相邻结构造成了严重压迫。患者最初表现为呼吸困难、胸痛和体重减轻。影像学检查显示有一个体积巨大、具有异质性特征、伴有钙化和胸腔积液的肿块,而活检及组织病理学分析证实为符合孤立性纤维瘤的间叶组织增生。尽管进行了部分切除,但由于肿瘤体积大且粘连广泛,无法完全切除。术后组织学检查结果显示出恶性特征,包括高有丝分裂指数和轻度核异型性。患者拒绝辅助化疗和放疗,在四个月内复发。尽管缺乏化疗敏感性,但肿瘤局部进展,患者临床状况恶化。该病例突出了恶性SFTP诊断和管理中的挑战,强调了个体化治疗方案的重要性以及由于不完全切除后存在复发风险和预后不良而进行长期随访的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77a5/11893203/d9a6db7bcbd4/cureus-0017-00000078713-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77a5/11893203/e708762d4337/cureus-0017-00000078713-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77a5/11893203/c7db577a5d07/cureus-0017-00000078713-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77a5/11893203/d9a6db7bcbd4/cureus-0017-00000078713-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77a5/11893203/e708762d4337/cureus-0017-00000078713-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77a5/11893203/c7db577a5d07/cureus-0017-00000078713-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77a5/11893203/d9a6db7bcbd4/cureus-0017-00000078713-i04.jpg

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