先天性霍纳综合征不会改变利氏结节的形成。

Congenital Horner's syndrome does not alter Lisch nodule formation.

作者信息

Mindel J S, Rubenstein A E, Wallace S, Aron A M, Halperin J

机构信息

Department of Ophthalmology, Mount Sinai Medical Center, New York, NY.

出版信息

Ann Neurol. 1994 Jan;35(1):123-4. doi: 10.1002/ana.410350121.

DOI:10.1002/ana.410350121

PMID:8285584

Abstract

A 21-year-old woman with neurofibromatosis type 1 (NF-1) had a unilateral congenital Horner's syndrome with resultant hypopigmentation of the affected iris. Lisch nodules, which are melanocytic hamartomas, were similar in number, size, and pigmentation in both eyes. The present findings suggest that the formation of Lisch nodules is not influenced by the presence or absence of sympathetic innervation of the iris.

摘要

一名患有1型神经纤维瘤病（NF-1）的21岁女性患有单侧先天性霍纳综合征，导致患侧虹膜色素减退。Lisch结节是黑素细胞错构瘤，双眼的数量、大小和色素沉着相似。目前的研究结果表明，Lisch结节的形成不受虹膜交感神经支配的有无影响。