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.
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http://dx.doi.org/10.7759/cureus.78713 | DOI Listing |
Cureus
February 2025
Thoracic Surgery, Mohammed VI University Hospital, Marrakesh, MAR.
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.
View Article and Find Full Text PDFJ Nucl Med
March 2025
Department of Diagnostic Radiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore;
Solitary fibrous tumor (SFT) is a rare sarcoma of mesenchymal origin. Although generally benign, SFTs carry the risk of recurrence and metastasis, with limited effective treatment options. The aims of this study are to compare the performance of fibroblast activation protein inhibitor (FAPI), [Ga]Ga-DOTA-FAPI-04 (denoted as [Ga]Ga-FAPI-04), and conventional [F]FDG PET/CT in patients with recurrent or metastatic SFTs head to head and to preliminarily explore the value of FAP-targeted radiopharmaceutical therapy with Lu for SFT patients.
View Article and Find Full Text PDFJ Oral Biol Craniofac Res
February 2025
Department of Oral and Maxillofacial Surgery, Post Graduate Institute of Dental Sciences, Rohtak, 124001, Haryana, India.
Solitary fibrous tumor (SFT) is a rare, benign spindle-cell neoplasm initially thought to be of mesothelial origin but later recognized as mesenchymal. While uncommon in the head and neck region, SFTs typically present in the oral cavity, orbit, and paranasal sinuses. The tumor's imaging characteristics, such as those seen in ultrasound and MRI, can often mimic vascular lesions, leading to diagnostic challenges.
View Article and Find Full Text PDFMed Ultrason
March 2025
Department of Ultrasound, The Second Affiliated Hospital of Dalian Medical University, Dalian, China.
Front Oncol
February 2025
Department of Radiology, Cancer Hospital of Shantou University Medical College, Shantou, China.
Objective: Solitary fibrous tumor (SFT) is an uncommon mesenchymal neoplasm that exhibits a broad spectrum of biological behaviors. Few studies relative to clinical-pathologic features and radiologic manifestations of SFTs have been reported. This study aimed to correlate the radiologic findings of SFTs with the clinical and histopathologic features.
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