颅骨孤立性肌纤维瘤病：一例病例报告及文献复习
Solitary myofibromatosis of the skull: a case report and review of literature.
作者信息
Tsuji Masayuki, Inagaki Takayuki, Kasai Harubumi, Yamanouchi Yasuo, Kawamoto Keiji, Uemura Yoshiko
机构信息
Department of Neurosurgery, Kansai Medical University, 10-15 Fumizono, 570-8507 Moriguchi, Osaka, Japan.
出版信息
Childs Nerv Syst. 2004 May;20(5):366-9. doi: 10.1007/s00381-003-0874-2. Epub 2004 Jan 14.
CASE REPORT
We present a case of solitary myofibromatosis of the skull in a 4-year-old girl. Surgery was performed and the final diagnosis of myofibromatosis was made histopathologically.
DISCUSSION
Solitary myofibromatosis of the skull is rare and we found approximately 20 reported cases in the English-language literature. We reviewed eight well-described cases.
CONCLUSION
Neuroradiologically, common features such as a lytic lesion with a sclerotic rim on roentgenogram and intra-diploic lesion with periosteal new bone formation both in the outer and inner table of the skull on computed assisted tomography are noticed.
病例报告
我们报告一例4岁女童的颅骨孤立性肌纤维瘤病。实施了手术，并通过组织病理学做出了肌纤维瘤病的最终诊断。
讨论
颅骨孤立性肌纤维瘤病很罕见，我们在英文文献中发现约20例报道病例。我们回顾了8例描述详尽的病例。
结论
在神经放射学方面，注意到一些常见特征，如X线片上有硬化边缘的溶骨性病变，以及计算机断层扫描显示颅骨内外板均有板障内病变伴骨膜新生骨形成。
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