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Cross Section of the Brain-Gray matter |
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Cortex—neuron, support cells Deep parts of the brain—basal ganglia, thalamus, hypothalamus |
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Beneath the cortex—myelinated axons |
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Frontal lobe—motor functions, behavior, emotions, higher intellectual functions Parietal lobe—sensory functions Temporal lobe—hearing, smelling Occipital lobe—visual center Thalamus—integration of sensory stimuli Hypothalamus—connects and regulates many body functions |
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Midbrain—visual and auditory reflex centers Medulla oblongata—cardiac, vasomotor, respiratory centers Pons |
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Major regulator of motor activities Integration of sensory impulses from the spinal cord and vestibular organ and motor impulses from the cerebral cortex |
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Normal Cells of the Nervous System |
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Neuron Perikaryon Dendrites Axon Support cells (glia) |
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Overview of Major Diseases |
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Developmental and genetic diseases Diseases caused by trauma Circulatory disorders Infectious diseases Autoimmune diseases Metabolic and nutritional diseases Neurodegenerative diseases of unknown etiology Brain tumors |
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The nervous system consists of highly specialized functional units. The CNS is protected from mechanical injury by the bones of the skull and vertebrae. The CNS is separated from the remainder of the body by meninges and by a blood–brain barrier. The brain and the spinal cord are surrounded by CSF. |
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Neurons are nondividing, postmitotic, permanent cells. Glial cells are facultative, mitotic (labile) cells that are capable of dividing. The CNS may be affected not only by diseases that involve other organs but also by diseases that are unique to the CNS. The symptoms of CNS diseases result from dysfunction of or loss of function of neurons. |
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Herniation of the cingulate gyrus Herniation of cerebral uncus Herniation of cerebral tonsil Herniation through an opening of a broken skull |
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Genetic diseases (e.g., Tay-Sach disease) Chromosomal abnormalities (e.g., Down’s syndrome) Intrauterine infections (e.g., TORCH syndrome) Anencephaly and dysraphic disorders (e.g., meningocele, myelomeningocele, spina bifida) |
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Epidural Subdural Subarachnoid Intracerebral |
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Between the skull and the dura Rupture of middle meningeal artery Coma Invariably lethal if unrecognized |
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Located between the dura and the arachnoid Most often caused by blunt trauma Source of bleeding—ruptured bridging veins Nonspecific symptoms (e.g., headache) caused by increased intracranial pressure |
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Located between the arachnoid and the pia layer of the meninges Caused by: Traumatic contusion of the brain Rupture of congenital (berry) aneurysms High mortality |
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Intracerebral Hemorrhages |
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Definition
Common complication of head trauma Rupture of intracerebral vessels Gunshot wounds Nontraumatic forms (e.g., stroke) Common in hematologic diseases (e.g., leukemia) |
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Third most common cause of death Most common crippling disease Most important clinical manifestation—stroke Disease of old age (atherosclerosis) Arterial hypertension Thromboembolism |
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Global ischemia Cerebral infarct Intracerebral hemorrhage |
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Lacunar infarcts Watershed infarcts Laminar necrosis |
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Caused by thrombotic occlusion and thromboemboli Encephalomalacia Pale infarct or hemorrhagic infarct Surrounding brain tissue that is edematous Fluid-filled cavity (“pseudocyst”) Clinical presentation as stroke (e.g., contralateral hemiplegia, sensory loss, global aphasia, drowsiness, stupor, coma) |
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Caused by arterial hypertension Basal ganglia Well-circumscribed hematoma Clinical features possibly resembling those of cerebral infarction |
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Brain injury Brain concussion Brain contusion Laceration Neck and spinal cord injuries Hyperextension injury Hyperflexion injury |
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Bacterial infections Hematogenous route or from septic emboli Caused most often by: Neisseria meningitidis Streptococcus pneumoniae Escherichia coli Haemophilus influenzae Treponema pallidum |
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Infections of the CNS-Viral |
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Definition
Hematogenous route Measles virus, rubella, adenovirus, herpesvirus, cytomegalovirus, rabies virus |
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Infections of the CNS-Protozoal |
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Definition
Hematogenous route Toxoplasma gondii |
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Infections of the CNS-Fungal |
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Definition
Hematogenous route Candida albicans, Aspergillus flavus, Cryptococcus neoformans |
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Encephalitis Myelitis Cerebral abscess Meningitis Neurosyphilis AIDS-related CNS lesions |
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Demyelinating disease Women affected twice as often as men Genetic factors Oligoclonal T-cell populations in the brain IgG in CSF composed of oligoclonal bands |
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Chronic disease Episodes of exacerbation and remission of neurologic symptoms Sensory abnormalities Loss of sensitization of touch Motor abnormalities Muscle weakness, unsteady gait, incoordination of movements, sphincter abnormalities Unpredictable course |
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Metabolic and Nutritional Diseases of the Nervous System |
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Definition
Inborn errors of metabolism Tay-Sachs disease, Niemann-Pick disease, phenylketonuria Nutritional disease Vitamin B1 deficiency (Wernicke-Korsakoff syndrome) Vitamin B12 deficiency (uncoordinated movements, sensorimotor peripheral neuropathy, signs of spinal cord disease, abnormal gait, psychiatric symptoms) Nicotinic acid deficiency (dermatitis, diarrhea, delirium) Alcoholism |
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Wernicke-Korsakoff syndrome Uncoordinated movements Progressive mental deterioration, loss of memory, inability to concentrate, irritability Subdural hematoma, pontine myelinolysis Delirium tremens |
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Neurodegenerative Diseases |
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Definition
Alzheimer’s disease Parkinson’s disease Huntington’s disease Amyotrophic lateral sclerosis |
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Unknown etiology Genetic factors—Down’s syndrome Atrophy of the cortical parts of the frontal and temporal parts of the brain Disease of older people (>70 years) Dementia—progressive loss of cognitive functions and a functional decline (loss of memory predominates) |
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Gross examination The brain appears atrophic and shows narrowing of the gyri and a widening of the sulci. Histologic changes Most prominent in the cortex Neuritic (senile) plaques Neurofibrillary tangles Granulovacuolar degeneration Deposition of amyloid in the neuritic plaques and the wall of the cerebral vessels |
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Subcortical neurodegenerative disorder Typically affects elderly persons Cause unknown Decreased number of dopaminergic neurons in the substantia nigra Disturbances of movement, primarily tumor, rigidity, bradykinesia, postural instability |
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Tremor or twitching of the muscles Instability while walking Depression and dementia Significant number of patients become depressed, and about 10% develop dementia. Gross examination Substantia nigra appears pale. Histologically Loss of melanin-rich neurons Lewy bodies |
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Autosomal dominant neurodegenerative disease Involuntary, gyrating movements and progressive dementia Atrophy of the cortex and subcortical nuclei, most prominently the caudate and putamen |
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Nonspecific histologic changes include: Atrophy, degeneration, loss of neurons, reactive gliosis First symptoms usually do not appear before midlife. Most affected patients become mentally incapacitated by the age of 50 to 60 years. |
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Amyotrophic Lateral Sclerosis |
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Definition
Neurodegenerative disease Affects older men and women Motor weakness and progressive wasting of muscles in the extremities (small hand muscles) Fasciculations (involuntary twitching) Slurred speech but the intellect is not affected |
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Amyotrophic Lateral Sclerosis |
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Definition
Loss of motor neurons in the spinal cord, midbrain, and cerebral cortex Loss of the lateral cerebrospinal pathways in the spinal cord Incurable, progressive disease that leads to death over a period of a few years |
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Brain tumors have a very high mortality rate. Brain tumors occur at any age. Of tumors, 50% are primary neoplasms They may be benign or malignant. Malignant tumors of the CNS do not metastasize. |
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Solid cerebral tumors in adults Cystic cerebellar tumors in children Composed of relatively well-differentiated astrocytes Progress into lesions that are histologically indistinguishable from glioblastoma multiforme |
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Most common CNS tumor Peak incidence—65 years Lateral hemispheres Gross appearance Parts of the tumor are necrotic and yellow Parts are hemorrhagic red, and parts are white Irregularly shaped Poorly demarcated Butterfly-like appearance |
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Histologically Highly anaplastic astrocytic cells Cell appearance—may retain a fetal appearance or become enlarged, bizarre shaped, or multinucleated with well-developed cytoplasm Numerous mitotic figures Proliferative changes of blood vessels |
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Cerebral hemispheres Middle-aged adults Well circumscribed, partially cystic, and calcified Histologically Well-differentiated oligodendroglia cells Possible progression to glioblastoma multiforme |
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Definition
Children—ventricles Adults—spinal cord Ependymoma of the filum terminale Tumor cells line the papillary structures or form rosettes |
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Tumors of Neural Cell Precursors and Undifferentiated Cells |
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Definition
Medulloblastoma Cerebellum Childhood Uncertain origin Poor prognosis |
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Arise from the meninges Mostly benign Located in the midline, at the base of the brain, and along the spinal cord Epileptic seizures or motor deficits Excellent prognosis |
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Tumors of the Cranial and Spinal Nerves |
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Definition
Neuromas Schwannomas (neurilemomas) Neurofibromas Solitary or multiple—mostly benign Neurofibrosarcomas rare Neurofibromatosis type II—involves cranial nerve, causing hearing loss and vertigo |
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Definition
Of all brain tumors, 50% represent metastases. They may be solitary or multiple. Most common tumors metastasizing to the brain are: Lung cancer Breast cancer Melanoma |
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