 |
Fig 1. There
are multiple eosinophilic spherical structures in the retina involving
all layers. These structures are present in a few ganglion cells,
but most appear to be floating "free" in the retinal
tissue. In fact, most of the structures are in cell processes
of the internal plexiform layer. |
| |
 |
Fig 2. The
spherical structures are brightly PAS positive |
| |
| Comment:
LaFora
bodies are polyglucosan accumulations that have been described
in the central nervous system of humans and animals. LaFora body
retinopathy has been described in humans, cats and dogs. The accumulation
in the retina of animals is usually not associated with clinical
signs and is thought to be a senile change. Lafora disease in
humans is an autosomal recessive disorder which affects carbohydrate
metabolism and results in a progressive, ultimately fatal neurological
condition called familial progressive myoclonus epilepsy. It is
characterized histologically by intraneuronal cytoplasmic polyglucosan
inclusions (Lafora bodies) in the retina and brain. The cat in
this case had no central nervous system signs and has not developed
any since the removal of her eye. An article in press by Dr. Greg
Hall (see references) describes polyglucosan bodies in the brain
of a seizuring cat. |
| Selected
References:
Kamiya
S; Suzuki Y. Polyglucosan bodies in the brain of the cat. J-Comp-Pathol.
101: 263-7, 1989
Hall DG;
WL Steffens; L Lassiter. Lafora Bodies Associated With Neurologic
Signs in a Cat. Vet Pathol. 35, May 1998 |
| Diagnosis:
Lafora Body Retinopathy |