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Erschienen in: BMC Ophthalmology 1/2018

Open Access 01.12.2018 | Case report

Embedding of lamellar hole-associated epiretinal proliferation combined with internal limiting membrane inversion for the treatment of lamellar macular hole: a case report

verfasst von: Yusuke Shiode, Yuki Morizane, Kosuke Takahashi, Shuhei Kimura, Mio Hosokawa, Masayuki Hirano, Shinichiro Doi, Shinji Toshima, Mika Hosogi, Atsushi Fujiwara, Fumio Shiraga

Erschienen in: BMC Ophthalmology | Ausgabe 1/2018

Abstract

Background

We recently reported that lamellar macular hole (LMH) with lamellar hole-associated epiretinal proliferation (LHEP) can be effectively treated by embedding the LHEP into the retinal cleavage to improve foveal contour and visual acuity. Here, we report a case of LMH with LHEP for which we performed embedding of the LHEP combined with internal limiting membrane (ILM) inversion. We then evaluated the effects of this surgery on macular morphology and visual functions.

Case presentation

A 62-year-old man presented with visual disturbance (20/29) and metamorphopsia in his right eye. B-scan optical coherence tomography (OCT) imaging revealed the presence of both partial-thickness defect of the macula with degenerative retinal cleavage and LHEP at the surface of the retina. En face OCT imaging showed the absence of retinal fold. We performed phacoemulsification with intraocular lens implantation, vitrectomy, embedding of LHEP into the retinal cleavage, and ILM inversion. Three months after the surgery, both foveal contour and visual acuity (20/20) were improved and metamorphopsia was reduced.

Conclusion

Embedding of the LHEP combined with ILM inversion may be an effective treatment for LMH with LHEP.
Hinweise

Electronic supplementary material

The online version of this article (https://​doi.​org/​10.​1186/​s12886-018-0926-8) contains supplementary material, which is available to authorized users.
Abkürzungen
BCVA
Best corrected visual acuity
ERM
Epiretinal membrane
ILM
Internal limiting membrane
LHEP
Lamellar hole-associated epiretinal proliferation
LMH
Lamellar macular hole
OCT
Optical coherence tomography
ONL
Outer nuclear layer
SS-OCT
Swept-source OCT

Background

Although an international classification of lamellar macular hole (LMH) based on B-scan images has been reported [1], the definition and classification of LMH has not yet reached a universal consensus because progressing optical coherence tomography (OCT) technology has revealed large morphological diversity of LMHs [28]. Recently, Govetto et al. [5] proposed that LMH can be classified into two types, tractional and degenerative, based on the presence or absence of retinal traction involvement. In support of this, our group combined radial B-scan OCT imaging and en face OCT imaging and observed that the pathology of degenerative LMH shows less involvement of retinal traction than the pathology of tractional LMH [9]. The difference in the pathologies of these LMH types suggests that differential treatment plans are necessary on the basis of retinal traction involvement. For tractional LMH, it is effective to remove the epiretinal membrane (ERM) and internal limiting membrane (ILM) in order to release retinal traction. However, the same treatment is unlikely to improve the pathology of degenerative LMH because of the lack of retinal traction involvement. Indeed, it has been reported that removal of the ERM and the ILM to treat degenerative LMH does not result in improved visual acuity or macular contour, and, furthermore, this surgery does result in an increased risk of macular hole formation [1012]. Therefore, an effective surgical treatment method for degenerative LMH is needed.
One of the features of degenerative LMH is the high probability of a yellow atypical ERM called a lamellar hole-associated epiretinal proliferation (LHEP) at the macula [24]. Histologically, LHEP is mainly composed of glial cells of the retina [12, 13]. Furthermore, observations during surgery for degenerative LMH have shown that that LHEP, unlike typical ERM, connects to the retina at the edge of the foveal aperture of the LMH [14]. These findings indicate that LHEP is composed of one of the major retinal glial cells, Müller cells, which have proliferated and migrated on the retinal surface with macular pigment [14].
To address the need for an effective surgical treatment for degenerative LMH, we previously proposed a surgical treatment method in which the LHEP is embedded in the retinal cleavage of the degenerative LMH. We found that this LMH embedding technique effectively improves both macular morphology and visual acuity [14]. Since glial cells proliferate and migrate to the site of nerve injury and contribute to nerve healing by producing trophic factors and growth factors [1518], the therapeutic mechanism of this procedure is probably due to the Müller cells within the embedded LHEP. Recently, using an experimental monkey model for large macular hole, we performed an ILM inversion technique and showed that the ILM, which is the basement membrane of Müller cells, was able to facilitate glial cell proliferation and migration as well as the expression of neurotrophic factors and growth factors from glial cells [19]. This technique thus lead to an acceleration of the wound healing processes at the macula [20]. Based on these findings, we hypothesized that the ILM might be able to facilitate the therapeutic process of the LHEP embedding technique for the treatment of degenerative LMH. In this report, we describe a case of degenerative LMH for which we performed the LHEP embedding technique combined with ILM flap inversion.

Case presentation

Presentation, history, and ocular examination

A 62-year-old man was referred to our clinic mainly for central visual disturbance and metamorphopsia in his right eye lasting more than 2 months. The patient had no significant history of systemic disease other than hypertension. At his initial visit, the best corrected visual acuity (BCVA) was 20/29 in his right eye and 20/17 in his left eye. The vertical and horizontal M-CHARTS (Inami & Co., Ltd., Tokyo, Japan) scores were 0.9° and 0.5° in the right eye, respectively. No distortion was detected by M-CHARTS in the left eye. A slit-lamp examination of the anterior segments revealed mild cataracts (grade I according to the Emery-Little classification) in both of his eyes. A fundus examination of his right eye showed a slightly reddish macula with a macular hole-like conformation (Fig. 1a).

OCT findings

As described in a previous report [9], the morphological features of the macula were identified by utilizing two swept-source OCT (SS-OCT) imaging methods (DRI OCT-1 Atlantis, TOPCON Corporation, Tokyo, Japan): radial B-scan imaging and en face imaging (Fig. 1b–e). The radial B-scan image confirmed the presence of partial-thickness defect of the macula with degenerative retinal cleavage as well as LHEP at the surface of the retina (Fig. 1b). The central retinal thickness was 156 μm, and the ellipsoid zone was almost continuous but showed an irregular reflection intensity. En face imaging revealed a membrane structure on the macula, but no retinal fold was observed (Fig. 1c and d). There was a retinal cleavage from the level of the ILM to the level of the outer nuclear layer (Fig. 1c–e). Based on these findings, we diagnosed the patient as degenerative LMH with LHEP.

Surgical procedure

To treat the case patient, we performed both LHEP embedment into the retinal cleavage as well as ILM inversion. Briefly, after performing phacoemulsification with intraocular lens implantation and a 25-gauge micro-incision vitrectomy, the LHEP was centripetally peeled off of the retina using intraocular forceps and was left attached to the edge of the LMH (Fig. 2a, b, e, f, i, and j). After trimming the LHEP using a vitreous cutter (Alcon Laboratories, Inc., Fort Worth, Texas) to fit the size of the retinal cleavage, the remnant LHEP was gently massaged centripetally over the LMH and thus embedded into the retinal cleavage (Fig. 2c, g, and k). Next, the ILM was visualized with indocyanine green and then peeled from the periphery towards the LMH. During this peeling, the ILM was not completely removed from the retina but was instead left attached to the edge of the LMH. The ILM was then inverted from upper to lower so that it completely covered the LMH with the embedded LHEP (Fig. 2d, h and l) [21]. During the ILM inversion, 1% low molecular weight hyaluronic acid (Opegan; Santen Pharmaceutical Co. Ltd., Osaka, Japan) was used to control the direction of the ILM flap inversion. Thereafter, sodium hyaluronate-chondroitin sulphate (Viscoat; Alcon Laboratories, Inc., Fort Worth, Texas) was placed on the inverted ILM in order to stabilize the flap. At the end of surgery, fluid-air exchange was performed, and the vitreous cavity was filled with 20% SF6 gas. Small amount of these viscoelastic substances (also known as ophthalmic viscosurgical devices) were intentionally left on the inverted ILM flap. The patient remained in the prone position for 3 days after the surgery. [See Additional file 1].
Additional file 1: After vitrectomy, the LHEP was centripetally peeled off of the retina using intraocular forceps and was left attached to the edge of the LMH. The LHEP was gently massaged centripetally over the LMH and thus embedded into the retinal cleavage. The ILM was peeled from the periphery towards the LMH but was not completely removed from the retina. The ILM was then inverted from upper to lower so that it completely covered the LMH with the embedded LHEP. During the ILM inversion, 1% low molecular weight hyaluronic acid was used to control the direction of the ILM flap inversion. At the end of surgery, fluid-air exchange was performed, and the vitreous cavity was filled with 20% SF6 gas. The patient remained in the prone position for 3 days after surgery. (MP4 24106 kb)

Post-operative recovery of the macula

One month after the surgery, both B-scan and en face OCT images showed that most of the retinal cleavage had disappeared (Fig. 1f–j). B-scan imaging showed the presence of embedded LHEP and inverted ILM, although it was difficult to distinguish these two from each other because they appeared to be integrated (arrowheads, Fig. 1g). Three months after the surgery, the foveal contour had further improved (Fig. 1k–o), and the ellipsoid zone had recovered (Fig. 1l, arrows). Furthermore, BCVA had improved to 20/20 and the vertical and horizontal M-CHARTS scores in the right eye had improved to 0.8° and 0°, respectively.

Discussion and conclusion

In this report, we show that combining the LHEP embedding technique with ILM inversion is an effective surgical treatment for degenerative LMH with LHEP. Two main reasons may explain why this combination of surgical techniques is more effective for treating LMH than the LHEP embedding technique alone. The first reason is that inverting the ILM makes it more likely that embedding the LHEP into the retinal cleavage will be successful. In the absence of an inverted ILM, there is a higher possibility that the embedded LHEP will move out of the retinal cleavage during fluid-gas exchange. In contrast, inverting the ILM and placing it over the LHEP can stabilize the LHEP into the retinal cleavage. The second reason this combination of surgical techniques might be more effective is that the inverted ILM might be expected to facilitate the healing effects of the embedded LHEP on the macula. LHEP is mainly composed of glial cells [12], which are thought to play a major role in the healing process of the macula when embedded into the retinal cleavage [14]. Recently, we performed ILM inversion to treat experimental macular hole in a monkey model. We found that the ILM, which is the basement membrane of Müller cells, functioned as a scaffold to promote the proliferation and migration of glial cells. Furthermore, the activated glial cells produced various neurotrophic factors as well as bFGF [20]. Therefore, it is reasonable to suppose that the inverted ILM might have acted as a scaffold of embedded glial cells and facilitated the repair process of the macula by glial cells in the current case.
Recent advances in OCT have revealed that LMH can be classified into two types based on the presence or absence of pathological retinal traction [5, 9]. LMHs that show pathological retinal traction are classified as tractional LMHs, while those that do not are classified as degenerative LMHs. Recently, we conducted an imaging study to ascertain the appearance rate of LHEP in both tractional and degenerative LMH and found that LHEP was only observed in degenerative LMH [9]. Therefore, the adaptation of the LHEP embedding technique described in this report can be applied only to degenerative LMH with LHEP. One important problem is that the appearance rate of LHEP in degenerative LMH is 80%, and no effective treatment for the 20% of degenerative LMHs that lack LHEP has been developed. Indeed, although ERM and ILM peeling to release retinal traction has been reported to be effective for treating tractional LMH, these techniques are not effective for treating degenerative LMH and may even be harmful as they can lead to postoperative macular hole [1012]. As discussed above, ILM inversion to treat degenerative LMH without LHEP may improve foveal contour and visual function by facilitating the activation of resident glial cells surrounding the LMH. Further study is required to assess the efficacy of ILM inversion for degenerative LMH without LHEP.
There are several limitations to the present report, wherein we describe only one case. The follow-up period is short, and there is a possibility that long-term follow-up will show the recurrence of LHEP or the development of secondary ERM. Furthermore, there is a risk that excessive proliferation of glial cells and inverted ILM may occur, resulting in scar formation at the macula and subsequent visual disturbance.
In conclusion, our case report suggests that combining the LHEP embedding technique with ILM inversion might be an effective treatment for LMH with LHEP. Further prospective studies involving a larger number of patients will be required to determine the actual efficacy of this technique.

Availability of data and materials

Data sharing is not applicable to this article as no datasets were generated or analysed during the current study.
This report was approved by the ethics committee at Okayama University. The case patient gave written, informed consent prior to undergoing surgery and for inclusion in this case study.
The case patient gave written, informed consent for publication of this report.

Competing interests

The authors declare that they have no competing interests.

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Anhänge

Additional file

Literatur
1.
Zurück zum Zitat Duker JS, Kaiser PK, Binder S, de Smet MD, Gaudric A, Reichel E, et al. The international Vitreomacular traction study group classification of vitreomacular adhesion, traction, and macular hole. Ophthalmology. 2013;120:2611–9.CrossRef Duker JS, Kaiser PK, Binder S, de Smet MD, Gaudric A, Reichel E, et al. The international Vitreomacular traction study group classification of vitreomacular adhesion, traction, and macular hole. Ophthalmology. 2013;120:2611–9.CrossRef
2.
Zurück zum Zitat Witkin AJ, Ko TH, Fujimoto JG, Schuman JS, Baumal CR, Rogers AH, et al. Redefining lamellar holes and the vitreomacular interface: an ultrahigh-resolution optical coherence tomography study. Ophthalmology. 2006;113:388–97.CrossRef Witkin AJ, Ko TH, Fujimoto JG, Schuman JS, Baumal CR, Rogers AH, et al. Redefining lamellar holes and the vitreomacular interface: an ultrahigh-resolution optical coherence tomography study. Ophthalmology. 2006;113:388–97.CrossRef
3.
Zurück zum Zitat Lai TT, Chen SN, Yang CM. Epiretinal proliferation in lamellar macular holes and full-thickness macular holes: clinical and surgical findings. Graefes Arch Clin Exp Ophthalmol. 2016;254:629–38.CrossRef Lai TT, Chen SN, Yang CM. Epiretinal proliferation in lamellar macular holes and full-thickness macular holes: clinical and surgical findings. Graefes Arch Clin Exp Ophthalmol. 2016;254:629–38.CrossRef
4.
Zurück zum Zitat dell'Omo R, Virgili G, Rizzo S, De Turris S, Coclite G, Giorgio D, et al. Role of lamellar hole-associated Epiretinal proliferation in lamellar macular holes. Am J Ophthalmol. 2017;175:16–29.CrossRef dell'Omo R, Virgili G, Rizzo S, De Turris S, Coclite G, Giorgio D, et al. Role of lamellar hole-associated Epiretinal proliferation in lamellar macular holes. Am J Ophthalmol. 2017;175:16–29.CrossRef
5.
Zurück zum Zitat Govetto A, Dacquay Y, Farajzadeh M, Platner E, Hirabayashi K, Hosseini H, et al. Lamellar macular hole: two distinct clinical entities? Am J Ophthalmol. 2016;164:99–109.CrossRef Govetto A, Dacquay Y, Farajzadeh M, Platner E, Hirabayashi K, Hosseini H, et al. Lamellar macular hole: two distinct clinical entities? Am J Ophthalmol. 2016;164:99–109.CrossRef
6.
Zurück zum Zitat Zampedri E, Romanelli F, Semeraro F, Parolini B, Frisina R. Spectral-domain optical coherence tomography findings in idiopathic lamellar macular hole. Graefes Arch Clin Exp Ophthalmol. 2017;255:699–707.CrossRef Zampedri E, Romanelli F, Semeraro F, Parolini B, Frisina R. Spectral-domain optical coherence tomography findings in idiopathic lamellar macular hole. Graefes Arch Clin Exp Ophthalmol. 2017;255:699–707.CrossRef
7.
Zurück zum Zitat Rino F, Elena Z, Ivan M, Paolo B, Barbara P, Federica R. Lamellar macular hole in high myopic eyes with posterior staphyloma: morphological and functional characteristics. Graefes Arch Clin Exp Ophthalmol. 2016;254:2141–50.CrossRef Rino F, Elena Z, Ivan M, Paolo B, Barbara P, Federica R. Lamellar macular hole in high myopic eyes with posterior staphyloma: morphological and functional characteristics. Graefes Arch Clin Exp Ophthalmol. 2016;254:2141–50.CrossRef
8.
Zurück zum Zitat Lai TT, Yang CM. Lamellar hole-associated epiretinal proliferation in lamellar macular hole and full-thickness macular hole in high myopia. Retina. 2018;38:1316–23.CrossRef Lai TT, Yang CM. Lamellar hole-associated epiretinal proliferation in lamellar macular hole and full-thickness macular hole in high myopia. Retina. 2018;38:1316–23.CrossRef
9.
Zurück zum Zitat Hirano M, Morizane Y, Kimura S, Hosokawa M, Shiode Y, Doi S, et al. Assessment of lamellar macular hole and macular Pseudohole with a combination of En face and radial B-scan optical coherence tomography imaging. Am J Ophthalmol. 2018;188:29–40.CrossRef Hirano M, Morizane Y, Kimura S, Hosokawa M, Shiode Y, Doi S, et al. Assessment of lamellar macular hole and macular Pseudohole with a combination of En face and radial B-scan optical coherence tomography imaging. Am J Ophthalmol. 2018;188:29–40.CrossRef
10.
Zurück zum Zitat Choi WS, Merlau DJ, Chang S. Vitrectomy for macular disorders associated with lamellar macular hole epiretinal proliferation. Retina. 2018;38:664–9.CrossRef Choi WS, Merlau DJ, Chang S. Vitrectomy for macular disorders associated with lamellar macular hole epiretinal proliferation. Retina. 2018;38:664–9.CrossRef
11.
Zurück zum Zitat Ko J, Kim GA, Lee SC, Lee J, Koh HJ, Kim SS, et al. Surgical outcomes of lamellar macular holes with and without lamellar hole-associated epiretinal proliferation. Acta Ophthalmol. 2017;95:e221–6.CrossRef Ko J, Kim GA, Lee SC, Lee J, Koh HJ, Kim SS, et al. Surgical outcomes of lamellar macular holes with and without lamellar hole-associated epiretinal proliferation. Acta Ophthalmol. 2017;95:e221–6.CrossRef
12.
Zurück zum Zitat Parolini B, Schumann RG, Cereda MG, Haritoglou C, Pertile G. Lamellar macular hole: a clinicopathologic correlation of surgically excised epiretinal membranes. Invest Ophthalmol Vis Sci. 2011;52:9074–83.CrossRef Parolini B, Schumann RG, Cereda MG, Haritoglou C, Pertile G. Lamellar macular hole: a clinicopathologic correlation of surgically excised epiretinal membranes. Invest Ophthalmol Vis Sci. 2011;52:9074–83.CrossRef
13.
Zurück zum Zitat Pang CE, Maberley DA, Freund KB, White VA, Rasmussen S, To E, et al. Lamellar hole-associated epiretinal proliferation: a Clinicopathologic correlation. Retina. 2016;36:1408–12.CrossRef Pang CE, Maberley DA, Freund KB, White VA, Rasmussen S, To E, et al. Lamellar hole-associated epiretinal proliferation: a Clinicopathologic correlation. Retina. 2016;36:1408–12.CrossRef
14.
Zurück zum Zitat Shiraga F, Takasu I, Fukuda K, Fujita T, Yamashita A, Hirooka K, et al. Modified vitreous surgery for symptomatic lamellar macular hole with epiretinal membrane containing macular pigment. Retina. 2013;33:1263–9.CrossRef Shiraga F, Takasu I, Fukuda K, Fujita T, Yamashita A, Hirooka K, et al. Modified vitreous surgery for symptomatic lamellar macular hole with epiretinal membrane containing macular pigment. Retina. 2013;33:1263–9.CrossRef
15.
Zurück zum Zitat Endo M, Ubulkasim G, Kobayashi C, Onishi R, Aiba A, Minami Y. Critical role of Ror2 receptor tyrosine kinase in regulating cell cycle progression of reactive astrocytes following brain injury. Glia. 2017;65:182–97.CrossRef Endo M, Ubulkasim G, Kobayashi C, Onishi R, Aiba A, Minami Y. Critical role of Ror2 receptor tyrosine kinase in regulating cell cycle progression of reactive astrocytes following brain injury. Glia. 2017;65:182–97.CrossRef
16.
Zurück zum Zitat Ridet JL, Malhotra SK, Privat A, Gage FH. Reactive astrocytes: cellular and molecular cues to biological function. Trends Neurosci. 1997;20:570–7.CrossRef Ridet JL, Malhotra SK, Privat A, Gage FH. Reactive astrocytes: cellular and molecular cues to biological function. Trends Neurosci. 1997;20:570–7.CrossRef
17.
Zurück zum Zitat Terenghi G. Peripheral nerve regeneration and neurotrophic factors. J Anat. 1999;194:1–14.CrossRef Terenghi G. Peripheral nerve regeneration and neurotrophic factors. J Anat. 1999;194:1–14.CrossRef
18.
Zurück zum Zitat Madduri S, Gander B. Schwann cell delivery of neurotrophic factors for peripheral nerve regeneration. J Peripher Nerv Syst. 2010;15:93–103.CrossRef Madduri S, Gander B. Schwann cell delivery of neurotrophic factors for peripheral nerve regeneration. J Peripher Nerv Syst. 2010;15:93–103.CrossRef
19.
Zurück zum Zitat Michalewska Z, Michalewski J, Adelman RA, Nawrocki J. Inverted internal limiting membrane flap technique for large macular holes. Ophthalmology. 2010;117:2018–25.CrossRef Michalewska Z, Michalewski J, Adelman RA, Nawrocki J. Inverted internal limiting membrane flap technique for large macular holes. Ophthalmology. 2010;117:2018–25.CrossRef
20.
Zurück zum Zitat Shiode Y, Morizane Y, Matoba R, Hirano M, Doi S, Toshima S, et al. The role of inverted internal limiting membrane flap in macular hole closure. Invest Ophthalmol Vis Sci. 2017;58:4847–55.CrossRef Shiode Y, Morizane Y, Matoba R, Hirano M, Doi S, Toshima S, et al. The role of inverted internal limiting membrane flap in macular hole closure. Invest Ophthalmol Vis Sci. 2017;58:4847–55.CrossRef
21.
Zurück zum Zitat Hirano M, Morizane Y, Kawata T, Kimura S, Hosokawa M, Shiode Y, et al. Case report: successful closure of a large macular hole secondary to uveitis using the inverted internal limiting membrane flap technique. BMC Ophthalmol. 2015;15:83.CrossRef Hirano M, Morizane Y, Kawata T, Kimura S, Hosokawa M, Shiode Y, et al. Case report: successful closure of a large macular hole secondary to uveitis using the inverted internal limiting membrane flap technique. BMC Ophthalmol. 2015;15:83.CrossRef
Metadaten
Titel
Embedding of lamellar hole-associated epiretinal proliferation combined with internal limiting membrane inversion for the treatment of lamellar macular hole: a case report
verfasst von
Yusuke Shiode
Yuki Morizane
Kosuke Takahashi
Shuhei Kimura
Mio Hosokawa
Masayuki Hirano
Shinichiro Doi
Shinji Toshima
Mika Hosogi
Atsushi Fujiwara
Fumio Shiraga
Publikationsdatum
01.12.2018
Verlag
BioMed Central
Erschienen in
BMC Ophthalmology / Ausgabe 1/2018
Elektronische ISSN: 1471-2415
DOI
https://doi.org/10.1186/s12886-018-0926-8

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