Abstract
Purpose:The purpose of this study was to describe the use of Descemet membrane anterior keratoplasty (DMAK) with modified allogeneic simple limbal epithelial transplantation to treat a case of partial limbal stem cell deficiency (LSCD) following keratolimbal allograft failure.Methods:Case report.Results:A 21-year-old woman with autoimmune polyglandular syndrome-related LSCD presented with pain and decreased vision. There was partial failure and recurrence of LSCD after a severe/acute keratolimbal allograft rejection that led to persistent epithelial defects refractory to conservative therapy. This was treated with a superficial keratectomy and placement of a DMAK. A modified allogeneic simple limbal epithelial transplantation was performed with an overlying amniotic membrane and temporary tarsorrhaphy. There was epithelialization of the corneal surface by 3 to 4 weeks with an improved ocular surface. Despite partial recurrence of late staining, the cornea has remained epithelized, vision has improved, and the patient has remained pain-free more than 1.5 years following the procedure.Conclusions:DMAK may be a long-term substrate to help improve and maintain epithelization of the cornea up to 1.5 years. DMAK may be a viable alternative to using amniotic membrane as a scaffold in allogeneic simple limbal epithelial transplantation for treatment of partial LSCD. While late epithelial staining recurred in our patient, DMAK appears to prevent recurrent epithelial defects and reduce ocular surface pain, conveying an improvement in quality of life in patients at high risk of rejection/failure.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 108-112 |
| Number of pages | 5 |
| Journal | Cornea |
| Volume | 44 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jan 1 2025 |
Bibliographical note
Publisher Copyright:Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.
Keywords
- Descemet membrane anterior keratoplasty
- allogeneic simple limbal epithelial transplantation
- autoimmune polyglandular syndrome
- keratolimbal allograft
- limbal stem cell deficiency
PubMed: MeSH publication types
- Case Reports
- Journal Article
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