Earley M J, Moriarty P, Yap L H
The Paediatric Craniofacial Unit, The Children's Hospital, Dublin, Ireland.
Br J Plast Surg. 2001 Mar;54(2):162-4. doi: 10.1054/bjps.2000.3512.
A patient with bilateral orbital neurofibromatosis is described. This patient had no other dysmorphic features and no systemic stigmata indicative of Von Recklinghausen's disease or endocrine syndromes. To our knowledge, this is the first report in the literature of isolated bilateral orbital neurofibromatosis in an otherwise normal patient.
本文描述了一名患有双侧眼眶神经纤维瘤病的患者。该患者没有其他畸形特征，也没有提示冯·雷克林霍增氏病或内分泌综合征的全身性体征。据我们所知，这是文献中首例关于一名其他方面正常的患者孤立性双侧眼眶神经纤维瘤病的报告。
