Brion S, Psimaras A, Chevalier J F, Plas J, Massé G, Jatteau O
Encephale. 1980;6(3):259-86.
An anatomoclinical case of Pick's Dementia secondarily complicated with Amyotrophic Lateral Sclerosis (A.L.S.) has been compared with twelve similar cases from the litterature. These comparisons drive to three hypotheses:--coincidence of two distinct diseases;--extension to motor cortex of the Pick's atrophy;--atypical onset of ALS outside of motor cortex, secondarily reaching the motor area. Against the last hypothesis, one could argue that, in "Pick's disease + ALS", there is no superficial spongiosis such as seen generally in ALS + Dementia in frontal or temporal cortex, or in ALS simplex in motor cortex. Also, there are marked focal lesions, i.e. in uncus hippocampi, similar to that of Pick's disease. However, if the second hypothesis seem to be the best one, there are actually no definite evidence for it.