Author/Authors :
Latifi, Golshan Cornea Department - Farabi Eye Hospital - Tehran University of Medical Sciences, Tehran, Iran , Katoozpour, Ramon Cornea Department - Farabi Eye Hospital - Tehran University of Medical Sciences, Tehran, Iran , Ghaffari, Reza Cornea Department - Farabi Eye Hospital - Tehran University of Medical Sciences, Tehran, Iran , Abdi, Parisa Cornea Department - Farabi Eye Hospital - Tehran University of Medical Sciences, Tehran, Iran , Kasiri, Maryam Cornea Department - Farabi Eye Hospital - Tehran University of Medical Sciences, Tehran, Iran , Berijani, Sahar Cornea Department - Farabi Eye Hospital - Tehran University of Medical Sciences, Tehran, Iran
Abstract :
Purpose: To evaluate the microstructural corneal changes during acute endothelial graft rejection and following treatment using in vivo
confocal microscopy (IVCM).
Methods: Patients with a clinical diagnosis of severe acute endothelial graft rejection following penetrating keratoplasty were included in this
study. IVCM was performed on the 1st day the patient presented with rejection signs and at the time of clinical resolution.
Results: Twenty‑three patients were included in this study. Inflammatory cells appeared as dendritic cells (DCs) and less frequently, as non‑DCs
in basal epithelial and subbasal areas. Activated keratocytes (AKs) (type 1: large cells with visible cytoplasmic processes; type 2: elongated and
spindle‑shaped keratocytes) were visible in acute phase. Following resolution, type 1 AKs considerably reduced, but type 2 cells were more
often persisted. Multiple types of keratic precipitates (KPs) were also visible in acute phase which resolved following resolution of rejection.
Conclusions: Acute graft rejection was associated with an increase in the number of DCs, activation of keratocytes, and aggregation of
various types of KPs. Inflammatory process subsided in almost all cases, but the IVCM changes did not return to normal early after clinical
resolution of rejection.
Keywords :
Activated keratocytes , Graft rejection , In vivo confocal microscopy , Keratic precipitate