Houcine Yoldez, Rais Abir, Kamoun Salma, Dhambri Sawssen, Jebali Souhaeil, Driss Maha
Pathology Department, Salah Azeiz Institute, 1006, Tunis, Tunisia.
Faculty of Medicine of Tunis, El Manar University, Tunis, Tunisia.
Discov Oncol. 2025 Jan 10;16(1):30. doi: 10.1007/s12672-024-01366-6.
Follicular dendritic cell sarcoma (FDCS) is a rare malignancy, often challenging to diagnose due to its nonspecific presentation and resemblance to other neoplasms. This case highlights a locally advanced nasopharyngeal FDCS initially misdiagnosed as a meningioma, underscoring the importance of differential diagnosis in unusual tumor presentations. A 77-year-old patient presented with nasal obstruction for 3 months. Imaging studies revealed a mass in the nasopharynx prolapsing into the oropharynx, leading to an initial diagnosis of meningioma based on its radiologic appearance. Surgical resection was performed, and histopathological examination, supplemented by immunohistochmical staining, revealed features consistent with follicular dendritic cell sarcoma. The tumor was locally advanced, involving surrounding structures, which complicated the initial clinical and radiologic assessment.
滤泡性树突状细胞肉瘤(FDCS)是一种罕见的恶性肿瘤,由于其表现不具特异性且与其他肿瘤相似,诊断往往具有挑战性。本病例突出了一例局部晚期鼻咽部FDCS,最初被误诊为脑膜瘤,强调了在不寻常肿瘤表现中进行鉴别诊断的重要性。一名77岁患者出现鼻塞3个月。影像学检查显示鼻咽部有一肿物突入口咽,基于其影像学表现初步诊断为脑膜瘤。进行了手术切除,组织病理学检查并辅以免疫组化染色,显示出与滤泡性树突状细胞肉瘤一致的特征。肿瘤为局部晚期,累及周围结构,这使得最初的临床和影像学评估变得复杂。