Son Gisung, Lee Ji Shin, Lee Suchan, Sohn Joonhong
Department of Ophthalmology, HanGil Eye Hospital, Incheon, Korea.
Department of Pathology, Chonnam National University Hwasun Hospital, Hwasun, Korea.
Korean J Ophthalmol. 2016 Dec;30(6):399-409. doi: 10.3341/kjo.2016.30.6.399. Epub 2016 Dec 6.
To discuss the unique morphology and origin of epiretinal proliferation associated with macular hole (EPMH) occasionally observed in full-thickness macular hole (FT-MH) or lamellar hole (LH) and to introduce the perifoveal crown phenomenon encountered when removing this unusual proliferative tissue.
Sixteen patients showing EPMH in spectral domain-optical coherence tomography were selected from 212 patients diagnosed with MH, LH, FT-MH, impending MH, macular pseudohole, or epiretinal membrane between January 2013 and December 2014. Of the 212 patients included for clinical analysis, 33, 23, 11, 7, and 190 exhibited LH, FT-MH, impending MH, macular pseudohole, and epiretinal membrane, respectively. We reviewed visual acuity, macular morphology, and clinical course. Surgical specimens were analyzed histologically.
EPMH presented as an amorphous proliferation starting from the defective inner/outer segment (IS/OS) junction covering the inner macula surface. Among the 16 patients with EPMH, 11 underwent vitrectomy, and all exhibited the intraoperative perifoveal crown phenomenon. EPMH tissue was sampled in three patients, one of whom had more tissue removed than intended and showed delayed recovery in visual acuity. Despite hole closure, IS/OS junction integrity was not successfully restored in four of 11 patients. Five patients were followed-up without surgical intervention. Visual acuity slightly decreased in three patients and did not change in one patient, while the remaining patient was lost during follow-up. Among the three perifoveal crown tissues obtained, two were successfully analyzed histologically. Neither tissue showed positivity to synaptophysin or S-100 protein, but one showed positivity to cytokeratin protein immunohistochemical staining.
EPMH exhibited a distinct but common configuration in spectral domain-optical coherence tomography. An epithelial proliferation origin is plausible based on its configuration and histological analysis. Perifoveal crown phenomenon was observed when removing EPMH during vitrectomy.
探讨在全层黄斑裂孔(FT-MH)或板层裂孔(LH)中偶尔观察到的与黄斑裂孔相关的视网膜前增殖(EPMH)的独特形态和起源,并介绍在切除这种异常增殖组织时遇到的黄斑中心凹周围冠现象。
从2013年1月至2014年12月期间诊断为MH、LH、FT-MH、即将发生的MH、黄斑假孔或视网膜前膜的212例患者中,选取16例在光谱域光学相干断层扫描中显示EPMH的患者。在纳入临床分析的212例患者中,分别有33例、23例、11例、7例和190例表现为LH、FT-MH、即将发生的MH、黄斑假孔和视网膜前膜。我们回顾了视力、黄斑形态和临床病程。对手术标本进行组织学分析。
EPMH表现为从覆盖黄斑内表面的缺陷性内/外节(IS/OS)连接处开始的无定形增殖。在16例EPMH患者中,11例接受了玻璃体切除术,所有患者均出现术中黄斑中心凹周围冠现象。3例患者获取了EPMH组织,其中1例切除的组织比预期多,视力恢复延迟。在11例患者中,有4例尽管裂孔闭合,但IS/OS连接处的完整性未成功恢复。5例患者未接受手术干预进行随访。3例患者视力略有下降,1例患者视力无变化,其余1例患者在随访期间失访。在获取的3个黄斑中心凹周围冠组织中,2个成功进行了组织学分析。两种组织突触素或S-100蛋白均无阳性表现,但一种组织细胞角蛋白免疫组化染色呈阳性。
EPMH在光谱域光学相干断层扫描中表现出独特但常见的形态。基于其形态和组织学分析,上皮增殖起源是合理的。在玻璃体切除术中切除EPMH时观察到黄斑中心凹周围冠现象。