SUMMARY: Dr. Russell Blaylock presents newly revealed Imaging and Pathologic data confirming his hypothesis that an Acute to Chronic inflammatory cascade, which he calls "Immuno-excitotoxicity" is the underlying cause of this disease process and other CNS degenerative diseases. It is initiated by vaccines, toxins, metabolic deficiencies, which can start this cascade with repeated insults to the cells as in boxing which has a similar immunoexcitotoxic basis leading to Parkinson,s disease. These repeated cellar traumatic episodes lead to a hyperactive state of the microglia in the CNS, the defense cells of the CNS, which then lead to a hyperactive excitatory series of chemical reactions that ultimately destroy the CNS cells and neurons. This hyperactive state of the microglia is called Microglial Priming, which Dr. Blaylock demonstrates in recently revealed work showing microglial activation on imaging studies. In addition to that discovery, a histopathological study, that was ignored from 20 years ago in people from young to 40 years of age with Autistic Spectrum Disorders, reveals the destruction of the neurons, axons, and other cells in the CNS. The authors also show that many inflammatory molecules were elevated as in immuno-excitotoxicity as described by Dr. Blaylock. These findings confirm his hypothesis that Immuno-excitotxicity is the pathological process behind the development of Autistic Spectrum Disorders. This disease has been described as having no known cause or treatment. This disease process is part of new molecular diseases of the 21st century. Should a neurosurgeon know about this new science? You decide. We did by publishing this work. These molecular diseases primarily involve the CNS.