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目的:分析总结下颌骨神经纤维瘤的临床及病理特点。方法:分析1例左下颌骨神经纤维瘤患者的临床资料,并检索和回顾分析相关中英文文献。结果:收集文献33篇,英文26篇,中文7篇,均为临床资料完整的个案报道,共计39例。结论:下颌骨神经纤维瘤是一种罕见的良性肿瘤,女性多见,缺乏特异性的临床表现,确诊依据病理和免疫组化。该肿瘤缺乏包膜,有一定的侵袭性,易复发,恶变少见,预后较好。
Objective: To analyze the clinical and pathological features of mandibular neurofibroma. Methods: The clinical data of 1 patient with left mandibular neurofibroma were analyzed and the related Chinese and English documents were retrieved and analyzed retrospectively. Results: There were 33 articles collected, 26 articles in English and 7 articles in Chinese. All of them were reported as complete clinical reports with a total of 39 cases. Conclusion: Mandibular neurofibroma is a rare benign tumor. It is common in women and lacks specific clinical manifestations. The diagnosis is based on pathology and immunohistochemistry. The tumor lacks the capsule, has some aggressiveness, is easy to relapse, malignant rare, the prognosis is good.