Central nervous system medulloepithelioma. A report of three cases

被引:4
作者
Bouhoula, A. [1 ]
Boubaker, A. [1 ]
Kallel, J. [1 ]
Chikili, R. [1 ]
Kchir, N. [2 ]
Khaldi, M. [1 ]
机构
[1] EPS Inst Natl Neurol, Serv Neurochirurg, Tunis 1007, Tunisia
[2] EPS Rabta, Serv Anat Pathol, Tunis, Tunisia
关键词
Primitive neuroectodermal tumor; Medulloepithelioma; Neural tube-like structures; Embryonic tumor; PRIMITIVE NEUROECTODERMAL TUMORS; CEREBRAL MEDULLOEPITHELIOMA; LONG SURVIVAL; IMMUNOHISTOCHEMISTRY; PERSPECTIVE; CHILDREN;
D O I
10.1016/j.neuchi.2010.03.003
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Central nervous system medulloepithelioma is a rare, highly malignant childhood tumor. It might be confused with medulloblastoma or other primitive neuroectodermal tumors, but it is quite particular by its clinical, radiological, and pathological features. The mean survival varies depending on whether or not a gross-total resection is possible. Adjuvant radiochemotherapy is often indicated. Only two reported cases in the literature survived beyond 4 years after treatment by gross total resection and radiotherapy without chemotherapy. We report three cases of supratentorial medulloepithelioma occurring in three children aged 11-17 years. Two patients underwent a gross-total resection followed by radiotherapy and survived more than 4 years after treatment. The third case had, however, recurred twice within the 1st postoperative month despite a complete resection each time and metastasis to the lung developed. Chemotherapy was then carried out after the third procedure and the patient died 7 months later. (C) 2010 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:395 / 400
页数:6
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