ArticleRadiology case reports2025
Intrapulmonary cavitating solitary fibrous tumor: A rare case report.
Article in Radiology case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
1 citing paper in PubMed.
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Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Solitary fibrous tumor (SFT) is a rare mesenchymal tumor that affects most commonly in the sixth or seventh decade of life. They account for less than 2% of all soft tissue tumors. In the thoracic region, it primarily appears in the pleura and rarely in the intrapulmonary. SFT typically presents as well-defined, oval or round, hyperdense masses. We report male 66-year-old complaint of cough, intermittent shortness of breath, and a lump in the lower right chest which has gradually increased in size. From chest MSCT results, there were cavitating lesions with solid and cystic components. FNAB and core biopsy examinations were performed. To establish a definitive diagnosis, an open biopsy followed by immunohistochemical analysis was conducted, confirming the presence of a solitary fibrous tumor (SFT).
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