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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。

Neoplasm of mixed mesenchymal and neuroepithelial origin: liposarcomatous meningioma combined with gliomas.

作者信息

Shuangshoti S

出版信息

J Neurol Neurosurg Psychiatry. 1973 Jun;36(3):377-82. doi: 10.1136/jnnp.36.3.377.

DOI:10.1136/jnnp.36.3.377
PMID:4351641
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC494336/
Abstract

A case is reported of an intracranial neoplasm of mixed mesenchymal and neuroepithelial (glial) origin occurring in the parieto-parasagittal region of the brain of a 19 year old man. A meningioma with liposarcomatous and psammomatous components comprised the mesenchymal part of the combined tumour. The neuroepithelial portion was composed of mixed ependymoma and astrocytoma. The combined neoplasm had the gross appearances and several microscopic features of giant-celled glioblastoma, giant cell sarcoma, and monstrocellular sarcoma. The findings suggest that these tumours have a mixed mesenchymal and neuroepithelial origin.

摘要

报告了一例发生在一名19岁男性大脑顶叶矢状旁区的混合性间充质和神经上皮(神经胶质)起源的颅内肿瘤。一个具有脂肪肉瘤和沙粒体成分的脑膜瘤构成了联合肿瘤的间充质部分。神经上皮部分由混合性室管膜瘤和星形细胞瘤组成。该联合肿瘤具有巨细胞胶质母细胞瘤、巨细胞肉瘤和怪异细胞肉瘤的大体外观和一些微观特征。这些发现提示这些肿瘤具有混合性间充质和神经上皮起源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3468/494336/013ad0f751a4/jnnpsyc00201-0061-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3468/494336/011b11e48470/jnnpsyc00201-0058-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3468/494336/7247ad6fc9a9/jnnpsyc00201-0059-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3468/494336/80a36c99a516/jnnpsyc00201-0060-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3468/494336/013ad0f751a4/jnnpsyc00201-0061-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3468/494336/011b11e48470/jnnpsyc00201-0058-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3468/494336/7247ad6fc9a9/jnnpsyc00201-0059-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3468/494336/80a36c99a516/jnnpsyc00201-0060-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3468/494336/013ad0f751a4/jnnpsyc00201-0061-a.jpg

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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。
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引用本文的文献

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Intracranial meningiomas associated with glial tumours: a review based on 54 selected literature cases from the literature and 3 additional personal cases.与胶质肿瘤相关的颅内脑膜瘤:基于54例文献精选病例及另外3例个人病例的综述
Acta Neurochir (Wien). 1991;110(3-4):133-9. doi: 10.1007/BF01400681.
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Primary intracranial rhabdomyosarcoma producing proptosis.

本文引用的文献

1
Liposarcoma: Report of a Case with Intracranial Metastases.脂肪肉瘤:一例颅内转移病例报告。
Am J Pathol. 1933 Nov;9(6):909-914.1.
2
Lipoma of the corpus callosum.胼胝体脂肪瘤。
J Neuropathol Exp Neurol. 1960 Apr;19:305-19. doi: 10.1097/00005072-196004000-00010.
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Glial origin of monstrocellular tumor. Case report of prolonged survival.巨大细胞瘤的神经胶质起源。长期生存病例报告。
原发性颅内横纹肌肉瘤导致眼球突出。
J Neurol Neurosurg Psychiatry. 1976 Jun;39(6):531-5. doi: 10.1136/jnnp.39.6.531.
4
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
J Neurol Neurosurg Psychiatry. 1979 Jun;42(6):524-8. doi: 10.1136/jnnp.42.6.524.
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Mixed mesenchymal and neuroectodermal tumor of the cerebellum.
Acta Neuropathol. 1978 Mar 15;41(3):261-3. doi: 10.1007/BF00690447.
J Neurosurg. 1967 Jan;26(1):72-7. doi: 10.3171/jns.1967.26.1part1.0072.
4
Dural liposarcoma associated with subdural hematoma. Case report.硬脑膜脂肪肉瘤合并硬脑膜下血肿。病例报告。
J Neurosurg. 1970 Jul;33(1):85-7. doi: 10.3171/jns.1970.33.1.0085.
5
Monstrocellular sarcoma of the brain: 6-year postoperative survival. Case report.脑巨细胞肉瘤:术后6年生存。病例报告。
J Neurosurg. 1969 Dec;31(6):686-9. doi: 10.3171/jns.1969.31.6.0686.
6
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.
7
Neoplasms of mixed mesenchymal and neuroepithelial type. With consideration of the relationship between meningioma and neurilemmoma.混合性间充质和神经上皮型肿瘤。兼论脑膜瘤与神经鞘瘤的关系。
J Neurol Sci. 1971 Nov;14(3):277-91. doi: 10.1016/0022-510x(71)90217-6.
8
Brain tumor of mixed mesenchymal and neuroepithelial origin. Case report.
J Neurosurg. 1971 Jun;34(6):808-13. doi: 10.3171/jns.1971.34.6.0808.