F,2d. | undefined hereditary syndrome, multiplied anomalies, sibling Acornea - keratopathy … missing Bowman membrane, disorganized stromal architecture
M,2m. | undefined hereditary syndrome, multiplied anomalies, sibling Bcornea - keratopathy … missing Bowman membrane, disorganized stromal architecture
M,48y. | cornea - Fabry disesase
F,72y. | melanoblastoma oculi
F,72y. | melanoblastoma oculi
F,72y. | melanoblastoma oculi
F,72y. | melanoblastoma oculi
F,69y. | cystadenoma (Warthin tumor) … caruncula - (modified mitochondria in an autolysed sample)
F,69y. | cystadenoma (Warthin tumor) … caruncula - (modified mitochondria in an autolysed sample)
M,17y. | Langerhans cell - eosinophilic granuloma (histiocytosis X) - orbita
F,12y. | liposarcoma v.s.- orbita
F,12y. | liposarcoma v.s.- orbita
M,15y. | neurinoma - orbita
M,15y. | neurinoma - orbita
M,15y. | neurinoma - orbita
M,15y. | neurinoma - orbita
M,68y. | auditory meatus … otitis externa mycotica
M,68y. | auditory meatus … otitis externa mycotica
M,68y. | auditory meatus … otitis externa mycotica - (toluidine-blue- stained semithin section)