神经鞘瘤

基本解释 (translations)

neurinoma  ·  neurilemmoma  ·  schwannoglioma

词组短语

glioma peripheral

与神经鞘瘤相关的网络例句 [注：此内容来源于网络，仅供参考]

There were 36 males and 40 females,with the average age of 47.7 years.36 patients presented with sciatica and perineal numbness,11 patients had painless mass and the other 20 were identified due to other causes.Among 67 benign neurogenic tumors,54 were originated from S1-S3 nerves,3 from S4-S5 nerves and 11 from the presacral space without caudal involvement.Giant cell tumor was found in 60 patients,which included 24 males and 36 females,with an average age of 32 years.Upper sacrum（S1-S2） was involved firstly.There were 56 patients（average,37.7 years） diagnosed as other primary benign bone tumors,which included 24 cases of teratomas,epidermoid cyst or dermoid cyst.Other malignant tumors,including chondrosarcoma （17）,Ewing′s sarcoma/PNET（14）,multiple myeloma（12）,lymphoma（6） and osteosarcoma（6） were found in 64 patients.

其中脊索瘤95例，男62例，女33例，平均年龄55.7岁，骶尾区疼痛是主要症状（82例），半数以上患者伴有坐骨神经痛，肿瘤多先累及低位骶骨（S3~S5）；神经源性肿瘤76例，男36例，女40例，平均年龄47.7岁，神经纤维瘤43例，神经鞘瘤24例，恶性神经鞘瘤9例，主诉多为坐骨神经痛、会阴部麻木（36例）和无痛性包块（11例），20例患者为查体或其他原因检查时发现，67例骶骨良性神经源性肿瘤起源于S3以上神经者54例，起源于S3以下神经者3例，发生于骶前未累及骶管者10例；骨巨细胞瘤60例，男24例，女36例，平均年龄32岁，腰骶尾部不适（37例）、坐骨神经痛（21例）是主要的临床表现，肿瘤多先累及上位骶骨（S1~S2）；骶骨其他原发良性肿瘤及瘤样病变56例，包括畸胎瘤、皮样囊肿、表皮样囊肿共24例；其他原发恶性肿瘤64例，包括软骨肉瘤17例，尤文肉瘤14例，多发性骨髓瘤12例，成骨肉瘤6例等。

Schwannoma; glial cells; glia; gliogenesis; glioma; peripheral nervous system; PNS; myelin sheath; saltatory impulse conduction; nodes of Ranvier; spinal cord

神经鞘瘤；胶质细胞；神经胶质；gliogenesis；神经胶质瘤；周围神经系统；PNS；髓鞘；跳跃冲动传导；郎飞氏结；脊髓

A total of 150 mesenchymal neoplasms of the GI tract, abdominal cavity, and retroperitoneum were retrieved from consult and surgical pathology archives, including 54 GISTs (8 KIT-negative; 13 desmin-positive), 17 GI leiomyosarcomas, 11 GI mural leiomyomas, 13 leiomyomas of the muscularis mucosae, 12 gastric schwannomas, 15 inflammatory myofibroblastic tumors, 9 cases of mesenteric desmoid fibromatosis, 10 dedifferentiated liposarcomas, and 9 malignant peripheral nerve sheath tumors.

我们从会诊病例及活检病例中找出150例间叶性肿瘤（来自胃肠道、腹腔和后腹膜），其中包括54例GISTs（8例KIT阴性、13例desmin阳性）、17例GI道平滑肌肉瘤、11例GI道肌壁间平滑肌瘤、13例GI道粘膜肌层平滑肌瘤、12例胃的神经鞘瘤、15例炎性肌纤维母细胞瘤、9例肠系膜韧带样纤维瘤、10例去分化型脂肪肉瘤和9例恶性外周神经鞘膜瘤。

None of the GISTs, desmoid tumors, inflammatory myofibroblastic tumors, schwannomas, dedifferentiated liposarcomas, or malignant peripheral nerve sheath tumors showed cytoplasmic reactivity for smoothelin.

所有GISTs、韧带样纤维瘤、炎性肌纤维母细胞瘤、神经鞘瘤、去分化脂肪肉瘤和恶性外周神经鞘膜瘤病例的瘤细胞浆均不表达smoothelin。

Results The study population consisted of 11 schwannomas,7 neurofibromas,1 ganglioneuroma,1neurofibromatosis,4 malignant schwannomas and 2 neurofibrosarcomas.

结果 神经鞘瘤 1 1例，神经纤维瘤 7例，节细胞神经瘤 1例，神经纤维瘤病 1例，恶性神经鞘瘤 4例和神经纤维肉瘤 2例。

All of these patients underwent plain and contrast-enhancement CT scan. Results: Thirteen cases included 5 neurilemmomas (3 malignant cases included), 5 neurofibromas, 1 neuroblastoma, 1 ganglioneuroma, 1 malignant paraganglioma. In the 13 cases, 2 cases derived from plexus sacralis, 2 cases located in the pelvic peritoneal space, 6 cases located in the pelvic extrapentoneal space, and 3 cases located in the vesica extraperitoneal space.

结果：神经鞘瘤5例（其中恶性3例），神经纤维瘤5例，神经母细胞瘤1例，节细胞性神经瘤1例，恶性副节细胞瘤1例。2例起源于骶丛，经由骶孔向盆腔内生长；2例起源于盆腔，其中1例源于膀胱，1例位于膀胱直肠陷窝；直肠腹膜外间隙6例；膀胱腹膜外间隙3例。

In particular,peripheral contrast enhancement with separations of an intradural extramedullaty tumor on MRI will suggest the diagnosis of schwannoma.

椎管内髓外硬膜下神经鞘瘤的MRI特征，有助于椎管肿瘤的鉴别诊断，尤其是伴有瘤内分隔性周围强化，应提示神经鞘瘤。

Results: Although most cases (11/16) were typical and clearly classified on MRI, atypical cases were also observed, such as meningioma of long T1/T2 signal intensity with small cystic foci, and neurinoma of iso intensity and homogenous enhancement without cystic change or enlargement of internal acoustic meatus.

结果：尽管多数神经鞘瘤(5/8)和脑膜瘤(6/8)具有典型的MRI表现特征并仅经MRI即可得到正确鉴别，但部分病例(5/16)为不典型表现者，如脑膜瘤呈长T1长T2信号并伴有囊变，以及神经鞘瘤呈等信号、均匀强化且不伴有囊变或内听道扩大者，鉴别诊断困难。

Benign nerve sheath tumors include neurofibromas, schwannomas, and perineuriomas.

良性神经鞘膜肿瘤包括神经纤维瘤、神经鞘瘤和神经束膜瘤。

In acoustic neuromas, patients with LOH were younger at the age of diagnosis, and larger tumor size, had shorter history and higher growth rate. Conclusions CHR22 LOH was a frequent event in the tumorigenesis of sporadic schwannoma. The presence of CHR22 LOH was related to clinical features.

CHR22 杂合子丢失是神经鞘瘤发生中的常发事件，缺失的区域包括NF2基因，CHR22 杂合子丢失与听神经瘤的临床行为有一定的关系，CHR22 杂合子丢失可能是神经鞘瘤增殖的重要因素。

与神经鞘瘤相关的网络解释 [注：此内容来源于网络，仅供参考]

neurilemma cell：神经鞘细胞

\\"神经鞘,神经膜\\",\\"neurilemma\\" | \\"神经鞘细胞\\",\\"neurilemma cell\\" | \\"神经鞘瘤\\",\\"neurilemmoma\\"

malignant peripheral nerve sheath tumor, malignant schwa oma：神经鞘: 恶性周边神经鞘肿瘤

malignant mixed tumor | 唾液腺: 恶性混合瘤 | malignant peripheral nerve sheath tumor, malignant schwa oma | 神经鞘: 恶性周边神经鞘肿瘤 | malignant pheochromocytoma | 肾上腺髓质: 恶性嗜铬细胞瘤

ganglioneuroma：神经节瘤

目的提高临床对咽旁隙神经源性肿瘤(neurogenic tumors in parapharyngeal space)的诊治水平.方法对7例手术后病例的临床资料进行回顾性分析.结果7例咽旁隙神经源性肿瘤中,神经鞘膜瘤(neurilemmoma)4例,神经纤维瘤(neurofibroma)2例,神经节瘤(ganglioneuroma)1例.随访3-9年,

neurilemmitis：神经鞘炎

neurilemmalcell 神经膜细胞 | neurilemmitis 神经鞘炎 | neurilemmomaofbone 骨神经鞘瘤

neurinoma：[神经鞘瘤]

神经鞘瘤:(neurinoma)以神经膜(Schwann)细胞为主体的良性肿瘤,沿神经干发展,多见于头颈部和纵隔(神经较多),其次为肢体,上肢多于下肢. 肿瘤椭圆形,软,有包膜,在神经一侧凸起. 切面光滑灰口色. 显微镜下见棱形瘤细胞,均匀,

neurinoma：神经瘤

neurilemmoma 神经鞘瘤 | neurinoma 神经瘤 | neuritis 神经炎

teratomas：畸胎瘤

其它类型包括畸胎瘤(teratomas)、松果体细胞瘤(pineocytomas)和成松果体细胞瘤(pineoblastomas). 听觉神经瘤是听觉神经的良性肿瘤. 顾名思义,听觉神经掌管听觉. 神经里的细胞称为神经鞘细胞或施万细胞,因此这种肿瘤也称为神经鞘瘤.

Malignant peripheral nerve sheath tumour, MPNST：恶性外周神经鞘膜瘤

Malignant perineurioma 恶性神经束膜瘤 9571 /3 Ⅱ-Ⅲ | 4. Malignant peripheral nerve sheath tumour, MPNST 恶性外周神经鞘膜瘤 | Epithelial 上皮样型 9540 /3 Ⅱ-Ⅳ

malignant peripheral nerve sheath tumor, malignant schwannoma：神经鞘: 恶性周边神经鞘肿瘤

malignant mixed tumor 唾液腺: 恶性混合瘤 | malignant peripheral nerve sheath tumor, malignant schwannoma 神经鞘: 恶性周边神经鞘肿瘤 | malignant pheochromocytoma 肾上腺髓质: 恶性嗜铬细胞瘤

schwannoma,cranial nerve：神经鞘瘤,颅神经

parotid,pleomorphic adenoma 腮腺,多形性腺瘤 | schwannoma,cranial nerve 神经鞘瘤,颅神经 | other problems to be considered其他需要考虑的问题