Atypical Cellular Elements of Unknown Origin in the Subbasal Nerve Plexus of a Diabetic Cornea Diagnosed by Large-Area Confocal Laser Scanning Microscopy
Katharina A. Sterenczak,
Oliver Stachs,
Carl Marfurt,
Aleksandra Matuszewska-Iwanicka,
Bernd Stratmann,
Karsten Sperlich,
Rudolf F. Guthoff,
Hans-Joachim Hettlich,
Stephan Allgeier,
Thomas Stahnke
Affiliations
Katharina A. Sterenczak
Department of Ophthalmology, Rostock University Medical Center, 18057 Rostock, Germany
Oliver Stachs
Department of Ophthalmology, Rostock University Medical Center, 18057 Rostock, Germany
Carl Marfurt
Department of Anatomy, Cell Biology & Physiology, Indiana University School of Medicine-Northwest, Gary, Indianapolis, IN 46204, USA
In vivo large-area confocal laser scanning microscopy (CLSM) of the human eye using EyeGuidance technology allows a large-scale morphometric assessment of the corneal subbasal nerve plexus (SNP). Here, the SNP of a patient suffering from diabetes and associated late complications was analyzed. The SNP contained multiple clusters of large hyperintense, stellate-shaped, cellular-like structures. Comparable structures were not observed in control corneas from healthy volunteers. Two hypotheses regarding the origin of these atypical structures are proposed. First, these structures might be keratocyte-derived myofibroblasts that entered the epithelium from the underlying stroma through breaks in Bowman’s layer. Second, these structures could be proliferating Schwann cells that entered the epithelium in association with subbasal nerves. The nature and pathophysiological significance of these atypical cellular structures, and whether they are a direct consequence of the patient’s diabetic neuropathy/or a non-specific secondary effect of associated inflammatory processes, are unknown.