April 2011
Volume 52, Issue 14
Free
ARVO Annual Meeting Abstract  |   April 2011
In Vivo Confocal Microscopy Criteria for Limbal Stem Cell Deficiency (LSCD) Syndrome
Author Affiliations & Notes
  • Dario A. Victoria, Sr.
    Ocular Surface Group-IOBA, University of Valladolid, Valladolid, Spain
  • Beatriz E. Ramirez
    Ocular Surface Group-IOBA, University of Valladolid, Valladolid, Spain
  • Jose M. Herreras
    Ocular Surface Group-IOBA, University of Valladolid, Valladolid, Spain
  • Denise HiIeeto
    Ocular Surface Group-IOBA, University of Valladolid, Valladolid, Spain
  • M. Eugenia Mateo
    Ocular Surface Group-IOBA, University of Valladolid, Valladolid, Spain
  • Margarita Calonge
    Ocular Surface Group-IOBA, University of Valladolid, Valladolid, Spain
  • Footnotes
    Commercial Relationships  Dario A. Victoria, Sr., None; Beatriz E. Ramirez, None; Jose M. Herreras, None; Denise HiIeeto, None; M. Eugenia Mateo, None; Margarita Calonge, None
  • Footnotes
    Support  CIBER-BBN, Carlos III Health Institute, Spain. Junta de Castilla y León SAN 1178/2009. D. Victoria and B. Ramirez have scholarships from the Carolina Foundation, Ministry of Foreing Affairs, Spain
Investigative Ophthalmology & Visual Science April 2011, Vol.52, 5118. doi:
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      Dario A. Victoria, Sr., Beatriz E. Ramirez, Jose M. Herreras, Denise HiIeeto, M. Eugenia Mateo, Margarita Calonge; In Vivo Confocal Microscopy Criteria for Limbal Stem Cell Deficiency (LSCD) Syndrome. Invest. Ophthalmol. Vis. Sci. 2011;52(14):5118.

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Abstract

Purpose: : To define in vivo confocal microscopy (CM) image criteria for LSCD syndrome based on the differences between slit lamp examination (SLE) and CM characteristics of affected and non-affected eyes.

Methods: : Eleven patients with LSCD (6 unilateral and 5 bilateral) were examined using SLE and CM in central cornea and superior, inferior, nasal and temporal limbal areas. The following parameters were defined by SLE: presence of palisades of Vogt (PV) in the limbus and presence of conjunctivalization, corneal scarring, melting, calcification, and persistent epithelial defects in central cornea and limbus. Morphological parameters evaluated by CM were: i) characteristics of the different normal components of the PV: palisade ridges (PR), limbal crypts (LC), focal stromal projections, border of bright/dark cells, and ii) presence of the following abnormal findings: neovascularization (NV), epithelial metaplasia (EM), goblet cells, hyperreflective inflammatory cells, Langerhans cells, and epithelial cysts.

Results: : In 5 eyes with unilateral LSCD syndrome, CM evaluation of the healthy limbal areas demonstrated that PV were predominantly observed in the superior and inferior limbus (83.0%), which coincided with the observations obtained by SLE. In 11 eyes affected by total LSCD, PV were never detected by SLE; however CM detected PR and LC in 11.4% of cases in the superior, nasal, and inferior limbus, although the morphology of these residual palisade structures was atrophic compared to the normal ones. The most frequent pathological features detected by CM in central cornea and limbus were NV (92.7%), EM (98.2%) and presence of goblet cells (98.2%). These findings were consistent with conjunctivalization, which was the main characteristic detected in the same areas by SLE (94.5%).

Conclusions: : Our results indicate that CM is a valuable and efficient technique to clinically characterize patients with LSCD. The absence of PV in SLE does not correlate with absence of palisade structures by CM. The following findings are suggested as CM diagnostic criteria of LSCD syndrome: 1) in the limbal area: atrophy or absence of PV, 2) in the central cornea and limbus: presence of epithelial metaplasia, neovascularization, and goblet cells.

Keywords: microscopy: confocal/tunneling • imaging/image analysis: clinical • cornea: clinical science 
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