Decock Christian E, De Baere Elfride E, Bauters Wouter, Shah Akash D, Delaey Christophe, Forsyth Ramese, Leroy Bart P, Kestelyn Philippe, Claerhout Ilse
Department of Ophthalmology, Ghent University Hospital, De Pintelaan 185, B-9000 Ghent, Belgium.
Arch Ophthalmol. 2011 Dec;129(12):1564-9. doi: 10.1001/archophthalmol.2011.348.
To study the basis of defective levator palpebrae superioris (LPS) function in blepharophimosis-ptosis-epicanthus inversus syndrome (BPES), an autosomal dominant eyelid malformation sometimes associated with ovarian dysfunction.
Eight patients with molecularly proved BPES underwent high-resolution surface-coil 3-T magnetic resonance imaging before surgical intervention. The features of LPS muscle and adjoining connective tissue were compared with an age-matched control subject. During LPS resection for ptosis repair, detailed anatomic examination of the LPS was performed. Histopathologic characteristics were compared with normal control samples from a cadaver and a patient with simple severe congenital ptosis.
The most striking feature shown on magnetic resonance imaging was the thin, long anterior part of the LPS. During the operation, this consisted of a disorganized, thin, long aponeurosis. However, in the posterior part of the LPS, there was an organized thick structure suggestive of a muscle belly. Histopathologic examination revealed posteriorly well-formed striated muscle fibers in all patients with BPES but not in the control sample from the patient with simple severe congenital ptosis. These striated muscle fibers were comparable to those of the normal control tissue but were more intermixed with collagenous tissue and little fatty degeneration.
The presence of striated muscle fibers in LPS of patients with BPES contrasts with the fatty degeneration in patients with simple severe congenital ptosis. To our knowledge, this is the first study providing novel insights into the pathogenesis of the eyelid malformation in BPES through extensive imaging, anatomic study, and histopathologic testing in a unique cohort of patients with molecularly proved BPES.
研究睑裂狭小 - 上睑下垂 - 内眦赘皮综合征(BPES)中提上睑肌(LPS)功能缺陷的基础,BPES是一种常染色体显性遗传性眼睑畸形,有时与卵巢功能障碍相关。
8例经分子检测确诊的BPES患者在手术干预前行高分辨率表面线圈3-T磁共振成像检查。将LPS肌肉及其毗邻结缔组织的特征与年龄匹配的对照受试者进行比较。在进行上睑下垂修复的LPS切除术时,对LPS进行详细的解剖学检查。将组织病理学特征与来自尸体和单纯严重先天性上睑下垂患者的正常对照样本进行比较。
磁共振成像显示的最显著特征是LPS前部薄且长。手术中发现,这部分由杂乱、薄且长的腱膜组成。然而,在LPS后部,有一个结构有序的厚实结构,提示为肌腹。组织病理学检查显示,所有BPES患者的LPS后部均有发育良好的横纹肌纤维,而单纯严重先天性上睑下垂患者的对照样本中则没有。这些横纹肌纤维与正常对照组织的相似,但与胶原组织混合更多,脂肪变性较少。
BPES患者LPS中存在横纹肌纤维,这与单纯严重先天性上睑下垂患者的脂肪变性形成对比。据我们所知,这是第一项通过对一组经分子检测确诊的独特BPES患者进行广泛的影像学、解剖学研究和组织病理学检测,为BPES眼睑畸形发病机制提供新见解的研究。