Cardia E, Molina D, Zaccone C, la Rosa G, Napoli P
Sezione di Neurochirurgia Infantile, Policlinico Universitario, Messina, Italy.
Childs Nerv Syst. 1993 Jul;9(4):246-9. doi: 10.1007/BF00303579.
An unusual case of infantile myofibromatosis of the solitary type occurring in an intracranial location in a 48-day-old female infant is presented. To our knowledge, there are no other descriptions in the literature of infantile myofibromatosis with exclusively intracranial involvement. The immunohistochemical and electron microscopic findings confirm the myofibroblastic origin of the proliferation.
本文报告了一例罕见的孤立型婴儿肌纤维瘤病，发生于一名48日龄女婴的颅内。据我们所知，文献中尚无仅累及颅内的婴儿肌纤维瘤病的其他描述。免疫组化和电镜检查结果证实了该增生的肌成纤维细胞起源。
