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- storiform neurofibroma 楼房状神经纤维瘤
- Three patients of neurofibroma showed enlarging of the sacral foramina. 3例神经纤维瘤均显示骶孔扩大。
- These tumor cells were all with wavy or comma-shaped nuclei arranged in storiform or fascicular pattern. 肿瘤细胞有波浪或逗点状细胞核并排列成涡纹状或束状形式，高核染质和非典型有丝分裂非常显著。
- Tumors with sparse number of ganglion cells may be misdiagnosed as neurofibroma. 带有许多稀疏的神经节细胞的肿瘤可能会被误诊为神经纤维瘤。
- The tumor origin was the surrounding soft tissue.Pathology showed storiform type of MFH. 肿瘤起源为周围软组织，病理切片显示为恶性纤维组织细胞瘤中的贮藏形成型。
- We report the case of a primary tracheal neurofibroma causing symptoms of airway obstruction in a 29-year-old woman. 摘要我们在此报告一位二十九岁女性罹患原发性气管内神经纤维瘤而导致呼吸道阻塞症状的病例。
- We report the case of a primary tracheal neurofibroma causing symptoms of airway obstruction in a29- year-old woman. 摘要我们在此报告一位二十九岁女性罹患原发性气管内神经纤维瘤而导致呼吸道阻塞症状的病例。
- The storiform areas show variable (negative or weaker) staining for CD21, and there are many fewer CD20+ B cells in such areas. 这些花瓣样排列的细胞区域也显示不同的免疫组化CD21的改变和CD20+B细胞区(阴性或弱阳性).
- We report one rare case of tardy ulnar palsy caused by neurofibroma of the ulnar nervie. 在此，我们报告一例以尺神经压迫表现之神经纤维瘤之病例。
- The histology and negative staining for S100 are not consistent with schwannoma or neurofibroma. 组织学图像和S100的阴性又不支持神经鞘瘤和神经纤维瘤。
- Objective To improve diagnosis accuracy of atypical neurolemmoma and neurofibroma by analyzing CT and MRI features. 目的分析不典型神经鞘瘤和神经纤维瘤的CT和MRI表现,提高其诊断准确率。
- The histologic examination shows several areas with a storiform arrangement of spindly cells with indistinct cell borders, intermingled with some small lymphocytes. 镜下见有些区域的梭形细胞呈花瓣状排列,这些梭形细胞边界不清,伴有一些小的淋巴细胞
- A neurofibroma of the lingual nerve is a rare clinical finding, the most common lesion site of a lingual neurofibroma being the tongue. 摘要源自于舌神经之神经纤维瘤在临床上极为少见，病灶处以舌头最常出现。
- The complication of these two cases, tumor bleeding, resulted from highly vascular nature of neurofibroma with minor trauma (mass gravity). 这两个个案的合并症，主要致因于肿瘤的易脆性及高度的血管颁布，再加上肿瘤本身重量的重力拉扯，最后造成肿瘤组织的撕裂与肿瘤内出血。
- ResultsThere were 1 case of intestinal neurofibroma, 1 case of mesenteric neurofibromatosis and 2 cases ofposterior peritonecem neurilemmoma. 结果1例肠系膜多发性神经纤维瘤,1例为小肠巨大神经纤维瘤,1例后腹膜多发性神经鞘瘤,1例后腹膜单发性神经鞘瘤。
- Herein, we report a case of lingual nerve neurofibroma that presented as a submandibular mass, mimicking a submandibular gland tumor or solitary lymphadenopathy. 我们报告一位神经纤维瘤病的患者，以下颌部肿瘤为表现的临床病例，术前诊断为来自下颌腺或是淋巴腺之肿瘤。
- Histopathologically, the dermis showed loose storiform arrangement of collagen bundles in a myxoid matrix, with spindled or stellate-shaped fibroblast-like cells, moderately accentuated vasculature and an increased number of mast cells. 组织病理学在真皮可见似纤维母细胞之梭状细胞及星状细胞松散地散布在黏液样之基质中，血管构造及肥大细胞之量亦有增加。
- For a patient presenting with neurofibromatosis and a submandibular mass, a neurofibroma of nerve origin should be considered in the differential diagnosis. 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。
- Diffuse neurofibroma is a rare and uncommon variant form of neurofibroma, frequently occurring in the head, neck and trunk of children and young adults. 摘要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。
- 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. 器官移植可以有多种形式。一种被称作自体移植，即某个患者体内消耗性的组织由来自其体内另一部位的组织所取代。
