Tisch Matthias, Hengstermann Frank, Kraft Klaus, von Hinüber Gerd, Maier Heinz
Department of Otolaryngology-Head and Neck Surgery, Department of Pathology, Federal Armed Hospital, Ulm, Germany.
Ear Nose Throat J. 2003 Jul;82(7):507-9.
Follicular dendritic cell tumors are extremely rare. Only 17 cases have been previously described in the literature, and only three of them involved primary tumours of the oral cavity. We describe a new case of the latter, which occurred in a 51-year-old man who sought evaluation for a painless enlargement of his left palatine tonsil. The tonsil was excised, and histologic examination revealed that the tumor was a primary sarcoma that had arisen from the dendritic reticulum cells of the palatine tonsil. Postoperatively, the tumor site was treated with percutaneous irradiation (total dose: 70 Gy). After more than 5 years of follow-up, the patient showed no evidence of recurrence. We also discuss the salient features of the immunohistochemical examination.
滤泡性树突状细胞瘤极为罕见。此前文献中仅描述过17例,其中仅3例涉及口腔原发性肿瘤。我们描述了1例后者的新病例,发生在一名51岁男性身上,他因左侧腭扁桃体无痛性肿大前来求诊。扁桃体被切除,组织学检查显示该肿瘤是起源于腭扁桃体树突状网状细胞的原发性肉瘤。术后,肿瘤部位接受了经皮照射(总剂量:70 Gy)。经过5年多的随访,患者无复发迹象。我们还讨论了免疫组化检查的显著特征。