Department of Plastic Surgery, State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, Guangdong, China.
Chin Med J (Engl). 2009 Nov 20;122(22):2700-4.
Blepharophimosis ptosis epicanthus inversus syndrome (BPES) is a rare congenital ophthalmic disorder, characterized by congenital eyelid malformation including bilateral ptosis, shortening of the horizontal eyelid fissure, epicanthus inversus, and increased distance between the inner canthi. In this research, we studied the histological structure and ultrastructure of medial canthal ligament of patients with BPES.
Thirty patients with BPES who received plastic surgery at the Zhongshan Ophthalmic Center from March 2006 to January 2008 were studied. There were 17 males and 13 females with an average age of (8.73 +/- 3.37) years (3 - 31 years). The medial canthal ligaments of patients were collected during the plastic surgery to analyze the histological structure by hematoxylin and eosin (HE), Congo red, van Gieson's (VG), Masson trichrome and aldehyde-fuchsin staining. The ultrastructures of the medial canthal ligaments were also analyzed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Fifteen samples of medial canthal ligament from healthy persons with an average age of (9.02 +/- 3.12) years (6 - 30 years) were collected as a control group.
Morphological and histological study showed that the medial canthal ligaments of BPES patients were composed of collagen fibers, a few elastic fibers and striated muscles. The collagen fibers assemblies were disorganized and the fibrous connective tissues were undergoing hyaline degeneration. The karyopycnosis of fibroblasts was located among the collagen fibrils and the numbers of fibroblasts were decreased. Ultrastructural study with SEM showed that the collagen fibers were larger than normal, irregular and loose. Parts of the collagen fibers were broken and had a coarse surface. Ultrastructural study with TEM showed that the fibroblasts had less cytoplasm, fewer organelles and the nucleus displayed pyknosis.
The medial canthal ligament in BPES patients is composed chiefly of collagen fibers. The collagen fibers of medial canthal ligaments in BPES patients are disorganized and hyaline degeneration is present. The study revealed that the medial canthal ligament of BPES patients might have congenital dysplasia.
睑裂狭小-上睑下垂-内眦赘皮综合征(BPES)是一种罕见的先天性眼部疾病,其特征为先天性眼睑畸形,包括双侧上睑下垂、水平睑裂缩短、内眦赘皮和内眦间距增加。本研究探讨了 BPES 患者内眦韧带的组织学结构和超微结构。
回顾性系列病例研究。收集 2006 年 3 月至 2008 年 1 月在中山大学中山眼科中心行整形手术的 30 例 BPES 患者(17 男,13 女)的内眦韧带,平均年龄(8.73±3.37)岁(331 岁)。对患者的内眦韧带进行组织学分析,包括苏木精-伊红(HE)、刚果红、VG、Masson 三色和醛复红染色。同时,通过扫描电镜(SEM)和透射电镜(TEM)观察内眦韧带的超微结构。另收集 15 例正常同龄(平均年龄(9.02±3.12)岁,630 岁)人内眦韧带作为对照。
组织学和超微结构研究显示,BPES 患者的内眦韧带主要由胶原纤维、少量弹性纤维和横纹肌组成。胶原纤维排列紊乱,纤维结缔组织发生玻璃样变性,成纤维细胞的核固缩位于胶原纤维之间,成纤维细胞数量减少。SEM 显示,BPES 患者的胶原纤维比正常人大,排列不规则且疏松。部分胶原纤维断裂,表面粗糙。TEM 显示,BPES 患者的成纤维细胞胞质较少,细胞器较少,细胞核呈固缩。
BPES 患者的内眦韧带主要由胶原纤维组成。BPES 患者的内眦韧带胶原纤维排列紊乱,存在玻璃样变性。研究表明,BPES 患者的内眦韧带可能存在先天性发育不良。