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孤独内神经纤维瘤是罕见的，主要发生在颌骨。A solitary intraosseous neurofibroma is rare and mostly occurs in the mandible.

目的研究神经纤维瘤及巨大神经纤维瘤的整形外科治疗。Objective To study the plastic surgical treatment of neurofibroma and giant neurofibroma.

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组织学图像和S100的阴性又不支持神经鞘瘤和神经纤维瘤。The histology and negative staining for S100 are not consistent with schwannoma or neurofibroma.

单发性胃神经纤维瘤临床颇为少见，术前诊断困难。The isolated gastric neurofibroma is a rare disease and is difficult to be diagnosed before operation.

目的探讨臀股部巨大复发性神经纤维瘤患儿围手术期护理措施。Objective To summarize the experience of peri-operation nursing on pediatric recurrent macro- neurofibroma.

目的研究面部神经纤维瘤及面部巨大神经纤维瘤的整形和显微外科治疗。Objective To study the reconstructive and microsurgical treatment of facial neurofibroma and neurofibromatosis.

报告1例神经纤维瘤，患者男性，18岁，出生后左小腿出现褐色斑疹。The artiele reported a case of neurofibroma. The patient was a 18- year-old male with brown macule at left leg.

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结论神经纤维瘤采用整形外科方法切除修复，具有切除较彻底，修复塑形好的优点。Conclusion Plastic surgical treatment of neurofibroma can yield good results with complete excision and better reconstruction.

硬纤维瘤4例，皮脂腺囊肿2例，脂肪瘤2例，神经纤维瘤2例，混合性肿瘤2例。After biopsy, desmoid was found in4cases, sebaceous cyst in2cases, lipoma in2case, neurofibroma in2cases and mixed tumor in2cases.

甲神经纤维瘤的舌神经是一种罕见的临床表现，最常见的病变部位的神经纤维瘤被舌舌。A neurofibroma of the lingual nerve is a rare clinical finding, the most common lesion site of a lingual neurofibroma being the tongue.

弥漫性神经纤维瘤是一种相当少见的神经纤维瘤。好发于小孩与年轻人，较常侵犯的部位是头颈部与躯干部位。Diffuse neurofibroma is a rare and uncommon variant form of neurofibroma, frequently occurring in the head, neck and trunk of children and young adults.

脑膜瘤6例，胶质瘤4例，炎性肉芽肿2例，血管网织细胞瘤3例，脂肪瘤、三叉神经纤维瘤和寄生虫感染各1例。These lesions include 6 meningioma, 4 glioma, 2 inflammatory granuloma, 3 hemangioblastoma, 1 lipoma, 1 trigeminal neurofibroma and 1 parasite infection.

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因此罹患神经纤维瘤病的患者，出现下颌腺肿瘤时，分布于此处的神经所长出的神经纤维瘤亦须纳入鑑别诊断。For a patient presenting with neurofibromatosis and a submandibular mass, a neurofibroma of nerve origin should be considered in the differential diagnosis.

在此，我们报告一例舌神经神经纤维瘤是作为颌下腺肿块，模仿颌下腺肿瘤或孤立淋巴结肿大。Herein, we report a case of lingual nerve neurofibroma that presented as a submandibular mass, mimicking a submandibular gland tumor or solitary lymphadenopathy.

第二个病例是一个29岁的男性患者，她的脸中部和下部患有一种严重的毁容性肿瘤——神经纤维瘤。The second patient, a 29-year-old male, suffered from a seriously disfiguring facial tumor in the middle and lower parts of his face, classified as a neurofibroma.

本组8例中，骨母细胞瘤3例，脊索瘤2例，骨巨细胞瘤1例，血管内皮细胞瘤1例，恶性神经纤维瘤1例。In 8 cases, including 3 cases with osteoblastomas, 2 cases with chordoma, 1 case with giant cell tumor, 1 case with angioendothelioma, 1 case with malignant neurofibroma.

当他长大后，病情变得发展更快，更严重，并形成一个罕见的名叫丛状纤维神经瘤的大肿瘤，这个大肿瘤可以从他的肩膀和锁骨后面看到。But as he grew, the condition became so aggressive and severe that he developed a rare large tumor called a plexiform neurofibroma , visible from the back of his shoulder and collarbone.