Jackson I T, Carbonnel A, Potparic Z, Shaw K
Institute for Craniofacial Surgery, Providence Hospital, Southfield, Mich.
Plast Reconstr Surg. 1993 Jul;92(1):1-11. doi: 10.1097/00006534-199307000-00001.
In localized orbitotemporal neurofibromatosis, the treatment depends very much on the type and severity of the orbital involvement and on the functional state of the eye. The condition can be conveniently divided into three groups, each requiring different treatment: (1) orbital soft-tissue involvement with a seeing eye, (2) orbital soft-tissue and significant bony involvement with a seeing eye, and (3) orbital soft-tissue and significant bony involvement with a blind or absent eye. A total of 24 patients with a maximum of 12 years recurrence-free follow-up are presented.
在局限性眶颞部神经纤维瘤病中,治疗很大程度上取决于眼眶受累的类型和严重程度以及眼睛的功能状态。这种情况可方便地分为三组,每组需要不同的治疗:(1)有视力的眼睛出现眼眶软组织受累;(2)有视力的眼睛出现眼眶软组织和明显的骨质受累;(3)失明或无眼球的眼睛出现眼眶软组织和明显的骨质受累。本文报告了24例患者,最长无复发随访时间为12年。