Niimura K, Shirane R, Yoshimoto T
Department of Neurosurgery, Tohoku University School of Medicine, Sendai, Japan.
Childs Nerv Syst. 1997 Nov-Dec;13(11-12):629-32. doi: 10.1007/s003810050157.
Infantile myofibromatosis (IM) is a proliferative disorder of infancy and early childhood characterized by the nodular or diffuse growth of lesions that are comprised of a mixture of mesenchymal elements. Intracranial involvement is reportedly rare, only eight such patients having been reported to our knowledge. We report on a 4-year-old boy with intracranial IM with a mass in his left temporal bone. A previous report on intracranial IM proposed that the underlying dura mater should be resected because of the possibility of early recurrence. At surgery in this case, the tumor was noted to be located in the bone itself and did not arise from the underlying dura. Therefore, the underlying dura mater and venous sinus were preserved. The follow-up MRI showed no sign of recurrences. It may not to be necessary to resect the dura mater in patients with intracranial IM.
婴儿肌纤维瘤病(IM)是一种发生于婴儿期和幼儿期的增殖性疾病,其特征为病变呈结节状或弥漫性生长,由间充质成分混合组成。据报道,颅内受累情况罕见,据我们所知,仅有8例此类患者被报道。我们报告了一名4岁男孩,患有颅内IM,左颞骨有一肿块。之前一篇关于颅内IM的报告提出,鉴于早期复发的可能性,应切除下方的硬脑膜。在该病例的手术中,发现肿瘤位于骨本身,并非起源于下方的硬脑膜。因此,保留了下方的硬脑膜和静脉窦。随访MRI显示无复发迹象。对于颅内IM患者,可能无需切除硬脑膜。