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. 2001 Sep;85(9):1031–1033. doi: 10.1136/bjo.85.9.1031

Ipsilateral limbal translocation for treatment of partial limbal deficiency secondary to ocular alkali burn

M Nishiwaki-Dantas 1, P E Dantas 1, J R Reggi 1
PMCID: PMC1724135  PMID: 11520748

Abstract

BACKGROUND/AIM—Chemical ocular burn, especially by alkali, may result in damage to the limbal stem cells, fundamental in maintaining the integrity of ocular surface. Clinically, patients manifest abnormal conjunctival-corneal healing with peripheral neovessels, chronic epithelial defect, severe stromal inflammation, and conjunctivalisation of the corneal, which is characteristic of limbal deficiency. Penetrating keratoplasty has a poor prognosis in these cases. Available therapeutic options included limbal autograft and allograft transplantation associated or not with human amniotic membrane transplant. The authors propose an alternative treatment with ipsilateral autologous limbal transplantation, transferring the healthy portion of the limbus from the partially burned eye to the deficient area in patients with partial limbal deficiency secondary to alkali burn.
METHODS—Ipsilateral limbal autografts were performed in five patients with partial limbal deficiency secondary to alkali burn, transferring the healthy portion of the limbus to the burned area of the same eye, without intervening in the contralateral eye.
RESULTS—All cases had regression of the limbal deficiency with improvement of visual acuity to a minimum of 20/60-20/20 (partial), without complications during the follow up period (range 7-11 months).
CONCLUSION—Ipsilateral autologous limbal autograft is a therapeutic option for partial limbal deficient eyes.



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Figure 1  .

Figure 1  

Preoperative and postoperative photographic sequence of three patients undergoing ILT. (A) Patient 1 with 4+ conjunctival hyperaemia, central epithelial defect, corneal oedema, neovascularisation, and BCVA of hand movements. (B) Same patient 11 months after ILT. Stable ocular surface and BCVA of 20/40. (C) Patient 2 presenting with diffuse conjunctival hyperaemia and corneal opacity with epithelial oedema, neovascularisation, and severe stromal oedema. BCVA was hand movements. (D) Same patient 10 months after ILT. BCVA was 20/60. (E) Patient 3 presenting epithelial defect, corneal oedema, and stromal opacity compromising the third inferior section of the cornea. BCVA was 20/80. (F) Nine months after ILT BCVA was 20/20.

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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