ReviewJournal of cardiothoracic surgery2022
Resection of giant malignant solitary fibrous pleural tumor after interventional embolization: a case report and literature review.
Review in Journal of cardiothoracic surgery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
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Who cites it
15 citing papers in PubMed, 19 citations in OpenAlex.
- A Giant Solitary Fibrous Tumour Arising From the Right Hemidiaphragm Detected Incidentally During a Routine Health Checkup.Respirology case reports · 2026Article
- From Hypoglycaemia to Haemorrhage: A Case of Giant Pleural Solitary Fibrous Tumour With Doege-Potter Syndrome.Respirology case reports · 2026Article
- Solitary Fibrous Tumor of the Pleura Presenting as a Giant Thoracic Mass: A Case Report.Clinical case reports · 2025Article
- Article
- Solitary Fibrous Tumor of the Pleura: A Clinical Case of a Giant Malignant Tumor With Post-surgical Recurrence.Cureus · 2025Article
- Aggressive atypical cystic fibromatosis of the pancreas: a case report and literature review.Frontiers in oncology · 2025Article
- Case Report: Doege-Potter syndrome: a giant solitary fibrous pleural tumor causing severe hypoglycemia.Frontiers in oncology · 2025Article
- Preoperative Embolization in the Management of Giant Thoracic Tumors: A Case Series.Journal of personalized medicine · 2024Article
- Surgical management of giant solitary fibrous tumors of the pleura: Two case reports.International journal of surgery case reports · 2024Article
- Resection of pleural solitary fibrous tumors with distinct feeding vessels arising from the descending aorta: a case report.Journal of cardiothoracic surgery · 2024Article
- Case report: A case of giant malignant solitary fibrous tumor of the pleura with Doege-Potter's syndrome and review of the literature.Frontiers in oncology · 2024Article
- Successful resection of a hypervascular paravertebral solitary fibrous tumor of pleura preserving the artery of Adamkiewicz, which was detected on preoperative angiography.General thoracic and cardiovascular surgery cases · 2023Article
- Surgery for Solitary Fibrous Tumors of the Pleura: A Review of the Available Evidence.Cancers · 2023Review
- Myxoid solitary fibrous tumor with rapid growth due to increased mucinous components: a case report.General thoracic and cardiovascular surgery cases · 2023Article
- Not to be confused, this is a pleural fibroma: Case report and literature review.International journal of surgery case reports · 2022Article
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Authors and funding
7 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundSolitary fibrous tumor of the pleura (SFTP) is a rare mesenchymal tumor that arises at various sites and typically originates from the pleura. Most patients with SFTPs are asymptomatic, unless the tumor is large. Approximately 20% of SFTP cases are malignant. There are few reports on imaging diagnoses and interventional treatments of SFTP. Here, we report a case of a giant SFTP that exhibited malignant behavior and underwent successful resection after embolization of the main supply artery of the tumor. CASE PRESENTATION: We report a clinical case of a giant SFTP in a 66-year-old Chinese female patient complaining of chest tightness and cough for more than 2 months. Ten years ago, the patient had undergone a chest CT scan at a local hospital for cough. Computed tomography (CT) had revealed a mass in the right thoracic region, which was misdiagnosed as a pulmonary abscess by CT-guided biopsy. Therefore, the patient did not receive appropriate/complete treatment at that time. She was hospitalized again, because CT showed significant enlargement of the right thoracic mass, which caused her obvious symptoms of discomfort. The pathological results of CT-guided biopsy at our hospital confirmed SFTP. Considering the large size of the tumor and the rich blood supply, some of the main blood vessels were treated with embolization before surgical resection. A large tumor, about 23 cm × 16 cm × 15 cm in size, was then successfully removed by thoracic surgery. The diagnosis of malignant SFTP was confirmed by surgical pathology and immunohistochemistry.
conclusionImaging findings of SFTPs are not characteristic, especially when a tumor is large, the diagnosis is difficult, and the final diagnosis still depends on histological and immunohistochemical examinations. The two-stage surgical treatment described here, which involves first embolization of the main supplying artery of the large tumor and then complete surgical resection, is effective and safe for SFTPs. Whether needle biopsy or vascular embolization is performed, intervention plays a crucial role in the diagnosis and treatment of patients with SFTPs.
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