Nasr A M, Blodi F C, Lindahl S, Jinkins J
Am J Ophthalmol. 1986 Dec 15;102(6):779-87. doi: 10.1016/0002-9394(86)90408-3.
We studied a rare case of congenital myofibromatosis of the orbit as part of a generalized multicentric disease in a 5-month-old boy. The ultrasonographic and computed tomographic findings were those of a low-reflective, firm, vascularized, lesion with heterogeneous internal structure. The histopathologic findings showed vascular channels with large polygonal cells and transition toward myofibroblasts with interwoven collagen fiber bundles.
我们研究了一名5个月大男婴眼眶先天性肌纤维瘤病的罕见病例，该病例为全身性多中心疾病的一部分。超声和计算机断层扫描结果显示为一个低回声、质地坚硬、血管丰富、内部结构不均匀的病变。组织病理学结果显示血管通道内有大的多边形细胞，并向具有交织胶原纤维束的肌成纤维细胞转变。
