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尺神经恶性间叶瘤:神经鞘肉瘤与横纹肌肉瘤的联合肉瘤

Malignant mesenchymoma of ulnar nerve: combined sarcoma of nerve sheath and rhabdomyosarcoma.

作者信息

Shuangshoti S, Chongchet V

出版信息

J Neurol Neurosurg Psychiatry. 1979 Jun;42(6):524-8. doi: 10.1136/jnnp.42.6.524.

DOI:10.1136/jnnp.42.6.524
PMID:469559
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC490256/
Abstract

Malignant mesenchymoma within the right ulnar nerve of an 8 year old boy is described. The patient did not have stigmata of von Recklinghausen's neurofibromatosis. The growing and painful tumour was excised five and a half detection, and recurred five months later. Mingling of the nerve sheath sarcoma and rhabdomyosarcoma was noted within the same mass which was separated from the adjacent striated muscles. It is suggested that this mesenchymoma arose from mesenchymal cells or cells of mesenchymal type comprising the peripheral nerve sheath which is derived from ectomesenchyme of the neural crest.

摘要

本文描述了一名8岁男孩右侧尺神经内的恶性间叶瘤。该患者没有冯·雷克林豪森神经纤维瘤病的体征。生长且疼痛的肿瘤在发现五个半月后被切除,五个月后复发。在与相邻横纹肌分离的同一肿块内,观察到神经鞘肉瘤和平滑肌肉瘤的混合。提示这种间叶瘤起源于构成周围神经鞘的间充质细胞或间充质类型的细胞,而周围神经鞘源自神经嵴的外胚层间充质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f45/490256/57480897d1e2/jnnpsyc00086-0043-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f45/490256/de20fcf4b364/jnnpsyc00086-0041-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f45/490256/c57d6bd89fdf/jnnpsyc00086-0042-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f45/490256/57480897d1e2/jnnpsyc00086-0043-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f45/490256/de20fcf4b364/jnnpsyc00086-0041-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f45/490256/c57d6bd89fdf/jnnpsyc00086-0042-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f45/490256/57480897d1e2/jnnpsyc00086-0043-a.jpg

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Malignant mesenchymoma of ulnar nerve: combined sarcoma of nerve sheath and rhabdomyosarcoma.尺神经恶性间叶瘤:神经鞘肉瘤与横纹肌肉瘤的联合肉瘤
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引用本文的文献

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本文引用的文献

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SARCOMAS OF THE PERIPHERAL NERVES AND SOMATIC SOFT TISSUES ASSOCIATED WITH MULTIPLE NEUROFIBROMATOSIS (VON RECKLINGHAUSEN'S DISEASE).与多发性神经纤维瘤病(冯·雷克林豪森病)相关的周围神经和躯体软组织肉瘤
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Storiform neurofibromas of the skin, pigmented and nonpigmented.皮肤的 Storiform 神经纤维瘤,有色素沉着的和无色素沉着的。
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5
Parapharyngeal meningioma with special reference to cell of origin.咽旁脑膜瘤:特别涉及起源细胞
Ann Otol Rhinol Laryngol. 1971 Jun;80(3):464-73. doi: 10.1177/000348947108000327.
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Survival in malignant schwannoma. An 18-year study.恶性神经鞘瘤的生存率。一项为期18年的研究。
Cancer. 1971 Mar;27(3):720-9. doi: 10.1002/1097-0142(197103)27:3<720::aid-cncr2820270331>3.0.co;2-d.
7
Ossifying subcutaneous neurilemoma. Evidence that neurilemoma is of mesencymal origin.骨化性皮下神经鞘瘤。神经鞘瘤起源于间充质的证据。
J Med Assoc Thai. 1971 Jan;54(6):434-42.
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Neoplasms of mixed mesenchymal and neuroepithelial origin. Relation to "monstrocellular sarcoma" or "giant-celled glioblastoma".
J Neuropathol Exp Neurol. 1971 Apr;30(2):290-309. doi: 10.1097/00005072-197104000-00010.
9
Neural neoplasms in Thailand: a study of 2,897 cases.
Neurology. 1974 Dec;24(12):1127-34. doi: 10.1212/wnl.24.12.1127.
10
Neoplasm of mixed mesenchymal and neuroepithelial origin: liposarcomatous meningioma combined with gliomas.混合性间充质和神经上皮起源的肿瘤:脂肪肉瘤样脑膜瘤合并胶质瘤。
J Neurol Neurosurg Psychiatry. 1973 Jun;36(3):377-82. doi: 10.1136/jnnp.36.3.377.