Kc Sudeep, Poudyal Himani
Department of Radiodiagnosis and Imaging, Patan Academy of Health Sciences, Lalitpur, Nepal.
Department of Internal Medicine, Dhulikel Hospital, Dhulikhel, Kavre, Nepal.
Radiol Case Rep. 2024 Jul 27;19(10):4363-4368. doi: 10.1016/j.radcr.2024.06.087. eCollection 2024 Oct.
Solitary fibrous tumor (SFT) arising from adult mesenchymal stem cells is an uncommon vascular tumor of pelvic cavity. While initially thought to be confined to the pleura, pericardium, or peritoneum, recent studies have revealed that SFTs can develop in different areas of the body. Typically, SFTs grow slowly and may not present noticeable symptoms. In this 2 case study, we describe the clinical situation of a 46-year-old female patient and 68 years old male patient who complained of persistent pelvic pain and urinary symptoms respectively. Imaging tests revealed solitary fibrous tumor in the pelvic cavity which was confirmed on histopathology, an unusual location for this type of tumor. This case reports focusses on importance of early recognition and treatment in dealing with this rare tumor.
起源于成人间充质干细胞的孤立性纤维瘤（SFT）是一种罕见的盆腔血管肿瘤。虽然最初认为它局限于胸膜、心包或腹膜，但最近的研究表明，SFT可在身体的不同部位发生。通常，SFT生长缓慢，可能不会出现明显症状。在本病例研究中，我们描述了一名46岁女性患者和一名68岁男性患者的临床情况，他们分别抱怨持续的盆腔疼痛和泌尿系统症状。影像学检查显示盆腔有孤立性纤维瘤，经组织病理学证实，这是该类型肿瘤不常见的位置。本病例报告重点关注早期识别和治疗这种罕见肿瘤的重要性。
