小儿患者宫颈孤立性纤维瘤1例罕见病例：病例报告及文献复习
A Rare Case of Cervical Solitary Fibrous Tumor in a Pediatric Patient: Case Report and Literature Review.
作者信息
Becattini Eleonora, Sgarbanti Lorenzo, Bevacqua Giuseppina, Grespi Valentina, Conti Carlo
机构信息
Unit of Neurosurgery, Azienda Ospedaliera S. Maria, 05100 Terni, Italy.
Neurosurgery Unit, Department of Translational Medicine, University of Ferrara, 44121 Ferrara, Italy.
出版信息
NeuroSci. 2025 Jun 1;6(2):49. doi: 10.3390/neurosci6020049.
Solitary fibrous tumors (SFTs) are rare mesenchymal neoplasms of fibroblastic origin. In this study, we report a rare case of cervical SFT in a pediatric patient, a rare phenomenon since the incidence is particularly rare in pediatric patients according to the literature. Typical radiological features of the lesion may lead to misdiagnosis. Image study and immunohistochemistry are crucial for its correct diagnosis. Their imaging characteristics often resemble meningiomas or schwannomas, making differential diagnosis challenging. Immunohistochemical markers such as CD34 and STAT6 remain essential for definitive diagnosis.
孤立性纤维性肿瘤（SFTs）是起源于成纤维细胞的罕见间叶性肿瘤。在本研究中，我们报告了一例儿科患者的罕见宫颈SFT病例，这是一种罕见现象，因为根据文献，其发病率在儿科患者中尤为罕见。该病变的典型放射学特征可能导致误诊。影像学检查和免疫组织化学对于其正确诊断至关重要。它们的影像学特征通常类似于脑膜瘤或神经鞘瘤，这使得鉴别诊断具有挑战性。免疫组织化学标志物如CD34和STAT6对于明确诊断仍然至关重要。
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