Abteilung Augenheilkunde, Bereich Strabologie, Neuroophthalmologie und okuloplastische Chirurgie, Universitätsmedizin Göttingen, Deutschland.
Institut für Medizinische Statistik, Georg-August-Universität Göttingen, Universitätsmedizin Göttingen, Deutschland.
Klin Monbl Augenheilkd. 2022 Jan;239(1):57-63. doi: 10.1055/a-1721-2375. Epub 2022 Feb 4.
Report of clinical findings relating to the lacrimal system in congenital clinical anophthalmos and severe blind microphthalmos (MAC-complex patients).
A retrospective study of the notes of 207 consecutive patients treated surgically at least once with highly hydrophilic self-inflating expanders for MAC between 1998 and 2021. The lacrimal drainage system was always probed and irrigated under general anaesthesia before any other procedure was started.
64 patients were excluded due to possible misdiagnosis because of previous lid or orbit surgery elsewhere or due to missing data. The analysis therefore included 67 girls and 76 boys aged between 1 and 126 months (median age: 5 months). 72 patients presented with unilateral and 42 with bilateral anophthalmos, and 24 had unilateral and 5 bilateral microphthalmos; consequently, 286 orbits (of which, 190 with probable pathology) were available for assessment. In unilateral cases the lacrimal system on the normal side was never affected. On the anophthalmic or microphthalmic side the lacrimal system was normal in 68 orbits only (35.8%). The most frequent finding was canalicular stenosis (91 orbits; 48%). Common canaliculus stenosis was observed in 12 orbits (6.3%) and nasolacrimal duct obstruction in 9 orbits (4.7%). There were four cases of punctal aplasia, but no other anomalies. In unilateral MAC pathologic findings during lacrimal probing were found to be associated with anatomical malformation of the contralateral fellow eye. Only in unilateral anophthalmos there was a significant association with cleft lip and palate, which was not found in the three other groups.
In congenital clinical anophthalmos the lacrimal system is affected in up to 66.5% of cases, mostly due to canalicular stenosis. Even if there is no clear evidence of an embryological connection, this association is certainly not a random finding.
报告先天性临床无眼症和严重盲小眼球(MAC 综合征患者)的泪器系统临床发现。
回顾性分析 1998 年至 2021 年间至少接受过一次高亲水性自膨式扩张器治疗的 207 例连续患者的病历。在开始任何其他手术之前,始终在全身麻醉下探查和冲洗泪道。
64 例患者因之前在其他地方进行过眼睑或眼眶手术或因数据缺失而被误诊,因此被排除在外。因此,分析包括 67 名女孩和 76 名男孩,年龄在 1 至 126 个月之间(中位数年龄:5 个月)。72 例为单侧无眼症,42 例为双侧无眼症,24 例为单侧小眼球,5 例为双侧小眼球;因此,286 个眼眶(其中 190 个有可疑病变)可用于评估。在单侧病例中,正常侧的泪器系统从未受到影响。在无眼症或小眼球症侧,仅 68 个眼眶(35.8%)的泪器系统正常。最常见的发现是泪小管狭窄(91 个眼眶;48%)。12 个眼眶可见共同泪小管狭窄(6.3%),9 个眼眶可见鼻泪管阻塞(4.7%)。有 4 例泪点缺如,但无其他异常。在单侧 MAC 中,泪道探查发现的病理发现与对侧正常眼的解剖畸形有关。只有在单侧无眼症中,与唇腭裂有显著关联,而在其他三组中则没有。
在先天性临床无眼症中,泪器系统受影响的比例高达 66.5%,主要是由于泪小管狭窄。即使没有明确的胚胎连接证据,这种关联肯定不是随机发现。