Subscribe to RSS
DOI: 10.1055/a-2538-5596
Deposition of a Descemet-like Layer by Ectopic Corneal Endothelium – Ultrastructure of a Long-term Persistent Double Anterior Chamber after Complicated Deep Anterior Lamellar Keratoplasty (DALK)
Bildung einer Descemet-ähnlichen Matrixschicht durch ektope korneale Endothelzellen – Ultrastruktur einer lange persistierenden doppelten Vorderkammer nach komplikativer DALK
Introduction
Deep anterior lamellar keratoplasty (DALK) is a microsurgical approach for the selective removal of diseased corneal stroma with preservation of the patientʼs healthy endothelium. The main advantages over penetrating keratoplasty (PKP) are the absence of donor endothelium as a potential immune target, the preservation of endothelial cell density, especially in young patients, and the avoidance of open-sky complications [1], [2], [3]. However, interface clarity, and thus visual outcome, after DALK depends on the preparation of a thin, smooth and uniformly thick recipient bed [4], [5]. This requires deep stroma dissection, which carries the DALK-specific risk of unintentional perforation of the underlying recipientʼs Descemetʼs membrane (DM). In this case, the recipient bed is likely to be separated from the graft by the leaking aqueous humor, resulting in the formation of a so-called “double anterior chamber” (AC), with aqueous flow on either side of the detached host layer [6]. For reattachment of the layer and coverage of the leak, the tamponade with gas (rebubbling) is usually a sufficient treatment. In case of a persistent double AC, the surgical correction by PKP may be necessary [7].
Some DALK surgeons decide to not remove DM and endothelium of the donor lenticule in order to preserve the regularity of the posterior donor surface and to reduce mechanical trauma of the tissue during the preparation (so-called “donor Descemet-on DALK”). This practice, however, is likely to delay the healing process of the interface, to increase interface reflectivity, and to promote the persistence of a potential double AC [8], [9]. Moreover, the transplanted donor endothelium remains a potential target of immunological rejection, which neutralizes one of the main advantages of DALK. The majority of current DALK protocols advise the removal of the donor DM and endothelium [4], [10].
This article reports on a patient who developed a double AC after complicated Descemet-on DALK, which then presumably persisted for 12 years. This unusual constellation as well as the long period enabled adaptation processes of the co-transplanted donor endothelium to the microenvironment of the double AC. An excimer PKP was performed, and the excised tissue was examined by light and transmission electron microscopy (TEM).
Publication History
Received: 24 November 2024
Accepted: 06 February 2025
Article published online:
27 March 2025
© 2025. Thieme. All rights reserved.
Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany
-
References
- 1 Reinhart WJ, Musch DC, Jacobs DS. et al. Deep anterior lamellar keratoplasty as an alternative to penetrating keratoplasty a report by the american academy of ophthalmology. Ophthalmology 2011; 118: 209-218
- 2 Daas L, Hamon L, Ardjomand N. et al. [Excimer laser-assisted DALK: a case report from the Homburg Keratoconus Center (HKC)]. Ophthalmologe 2021; 118: 1245-1248
- 3 Daas L, Aljundi W, Abdin A. et al. Excimer Laser-Assisted Deep Anterior Lamellar Keratoplasty vs. Penetrating Keratoplasty for Patients With Keratoconus: A Retrospective Analysis From the Homburg Keratoconus Center (HKC). Cornea 2024; [accepted for publication]
- 4 Sarnicola E, Sarnicola C, Sarnicola V. Anterior Lamellar Keratoplasty: Current State of the Art. In: Alió JL, del Barrio JLA, eds. Modern Keratoplasty: Surgical Techniques and Indications Essentials in Ophthalmology. Cham: Springer International Publishing; 2023: 257-281
- 5 Berger T, Seitz B, Hamon L. et al. Ultrastructural Examination of the Corneal Interface after Predescemetic Deep Anterior Lamellar Keratoplasty (DALK) – A Case Report with Light and Transmission Electron Microscopy. Klin Monbl Augenheilkd 2023; 240: 1010-1016
- 6 Myerscough J, Bovone C, Mimouni M. et al. Factors Predictive of Double Anterior Chamber Formation Following Deep Anterior Lamellar Keratoplasty. Am J Ophthalmol 2019; 205: 11-16
- 7 Sarnicola C, Sarnicola E, Cheung AY. et al. Deep Anterior Lamellar Keratoplasty: Can All Ruptures Be Fixed?. Cornea 2023; 42: 80
- 8 Feizi S, Zare M, Hosseini SB. et al. Donor Descemet-off versus Descemet-on deep anterior lamellar keratoplasty: a confocal scan study. Eur J Ophthalmol 2015; 25: 90-95
- 9 Morrison JC, Swan KC. Full-thickness lamellar keratoplasty. A histologic study in human eyes. Ophthalmology 1982; 89: 715-719
- 10 Nanavaty MA, Vijjan KS, Yvon C. Deep anterior lamellar keratoplasty: A surgeonʼs guide. J Curr Ophthalmol 2018; 30: 297-310
- 11 Seitz B, Langenbucher A, Kus MM. et al. Nonmechanical corneal trephination with the excimer laser improves outcome after penetrating keratoplasty. Ophthalmology 1999; 106: 1156-1164
- 12 Jacobi C, Zhivov A, Korbmacher J. et al. Evidence of endothelial cell migration after descemet membrane endothelial keratoplasty. Am J Ophthalmol 2011; 152: 537-542.e2
- 13 Van Den Bogerd B, Dhubhghaill SN, Koppen C. et al. A review of the evidence for in vivo corneal endothelial regeneration. Surv Ophthalmol 2018; 63: 149-165
- 14 Vercammen H, Miron A, Oellerich S. et al. Corneal endothelial wound healing: understanding the regenerative capacity of the innermost layer of the cornea. Transl Res 2022; 248: 111-127
- 15 Joyce NC. Proliferative capacity of corneal endothelial cells. Exp Eye Res 2012; 95: 16-23
- 16 Joyce NC, Harris DL, Mello DM. Mechanisms of mitotic inhibition in corneal endothelium: contact inhibition and TGF-beta2. Invest Ophthalmol Vis Sci 2002; 43: 2152-2159
- 17 Senoo T, Joyce NC. Cell cycle kinetics in corneal endothelium from old and young donors. Invest Ophthalmol Vis Sci 2000; 41: 660-667
- 18 Mimura T, Joyce NC. Replication competence and senescence in central and peripheral human corneal endothelium. Invest Ophthalmol Vis Sci 2006; 47: 1387
- 19 Heindl LM, Schlötzer-Schrehardt U, Cursiefen C. et al. Myofibroblast metaplasia after descemet membrane endothelial keratoplasty. Am J Ophthalmol 2011; 151: 1019-1023.e2
- 20 Weller JM, Schlötzer-Schrehardt U, Tourtas T. et al. Influence of Ultrastructural Corneal Graft Abnormalities on the Outcome of Descemet Membrane Endothelial Keratoplasty. Am J Ophthalmol 2016; 169: 58-67
- 21 MacCallum DK, Lillie JH, Scaletta LJ. et al. Bovine corneal endothelium in vitro . Exp Cell Res 1982; 139: 1-13
- 22 Johnson DH, Bourne WM, Campbell RJ. The ultrastructure of Descemetʼs membrane. I. Changes with age in normal corneas. Arch Ophthalmol 1982; 100: 1942-1947
- 23 Murphy C, Alvarado J, Juster R. Prenatal and postnatal growth of the human Descemetʼs membrane. Invest Ophthalmol Vis Sci 1984; 25: 1402-1415
- 24 de Oliveira RC, Wilson SE. Descemetʼs membrane development, structure, function and regeneration. Exp Eye Res 2020; 197: 108090