Melanotic neuroectodermal tumor of infancy in the skull: case report and review of the literature

被引:22
作者
Matsumoto, M [1 ]
Sakuma, J [1 ]
Suzuki, K [1 ]
Kawakami, M [1 ]
Sasaki, T [1 ]
Kodama, N [1 ]
机构
[1] Fukushima Med Univ, Dept Neurosurg, Fukushima 9601295, Japan
来源
SURGICAL NEUROLOGY | 2005年 / 63卷 / 03期
关键词
infant; melanotic neuroectodermal tumor; skull; surgery;
D O I
10.1016/j.surneu.2004.02.032
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Melanotic neuroectodermal tumor of infancy (MNTI) is a rare neoplasm that develops during the first year of life and grows rapidly. Early diagnosis and radical surgery are critical for a long-term cure. We report a rare case of MNTI in the skull and discuss the importance of the radical surgery and the long-term follow-up results. Case Presentation: We describe a case of a 4-month-old girl with an MNTI in the skull who underwent the operation 11 years ago. The mass in the frontotemporosphenoid region grew rapidly after birth. The patient underwent a craniotomy. By referring to the histological findings of frozen section during surgery, a total excision of the tumor including its adjacent hypertrophic bone was performed. The patient has remained well without evidence of recurrence or neurological abnormality for 11 years. Conclusion: Radical surgery for MNTI provides complete cure. According to the literature including our case, there should be follow-up for at least 2 years after surgery. Especially in cases in which tumors recur, follow-up should be for longer periods because of the possibility of its malignant change. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:275 / 280
页数:6
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