1 / 31

Diseases of Nervous System

Diseases of Nervous System. Fatima Obeidat , MD. I. Patterns Of Injury In the Nervous System. A. Features of Neuronal Injury. 1. Red neurons : Within 12 hours of an irreversible ischemic injury, acute neuronal injury becomes evident on H&E stain and characterized by:

teresa
Télécharger la présentation

Diseases of Nervous System

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Diseases of Nervous System Fatima Obeidat, MD

  2. I. Patterns Of Injury In the Nervous System

  3. A. Features of Neuronal Injury 1. Red neurons: Within 12 hours of an irreversible ischemic injury, acute neuronal injury becomes evident on H&E stain and characterized by: a. Shrinkage of the cell body, pyknosis of the nucleus and Loss of Nissl substance b. Angulated nucleus and disappearance of nucleolus c. Intense eosinophilia of the cytoplasm

  4. RED NEURONS

  5. 2. Specific intranuclear inclusions a. Neurofibrillary tangles in Alzheimer disease b.. Lewy bodies in Parkinson disease c. Inclusions in viral infections: Example: Nigri bodies in Rabies

  6. Nigri bodies

  7. B. Astrocytes in Injury and repair 1.Astrocytes are the principal cells for repair and scar formation in the brain Gliosis: -The astrocytes undergo hypertrophy and hyperplasia in response to injury I. In early gliosis, astrocytes are called gemistocytes and Characterized by: A. Enlarged nucleus with prominent nucleolus B. Stout ramifying processes extend from the cell

  8. C. The scanty cytoplasm becomes abundant and pink II. In long standing gliosis ,there will be extensive formation of astrocyticglial filaments called gliotic scar III. Chaslin’sgliosis in subpial layer in epilepsy • Note: - Unlike else in the body fibroblasts participate to a limited extent in healing in brain and in the following situations: 1. Brain abscess 2. Penetrating trauma

  9. 2. Rosenthal fibers - Are thick elongated , eosinophilic aggregates found in processes of astrocytes , composed of Large amounts of glialfibrillary acidic protein (GFAP)and Ubiquitin and are prominent in the following: a. Chronic gliosis b. Pilocyticastrocytoma(inside the tumor) c. In the tissue surrounding: 1. Hemangioblastoma 2. Craniopharyngioma

  10. Gemistocytes Rosenthal fibers

  11. 3. Spinal syrinx d. Alexander’s disease: Activating mutation in GFAP gene 3. Corpora amylacea: - Are spherical laminated bodies composed of polyglucosan - Most abundant close to pia, around blood vessels and adjacent to ependymal lining - Their accumulation is associated with aging and in response to neuronal loss - Stain positive with PAS

  12. Corpora amylacea

  13. C. Microglial cells - Are bone marrow derived cells - Function as the resident phagocytes of the CNS - Microglial cells take on the appearance of activated macrophages in areas of 1. Demyelination 2.Organizing infarct 3. Hemorrhage

  14. Notes I. Rod cells : are microglial cells having elongated nuclei in cases of neurosyphilis II. Microglial nodules: are aggregates of microglial cells around brain injury (viral infection) such as in HIV encephalitis II.Neuronophagia: aggregation of microglial cells around and phagocytosing injured neurons such as in poliomyelitis

  15. Microglial Nodules Neuronophagia

  16. D. Ependymal cells - Have limited capacity to regeneration - Once the ependynal surface is broken due to stretching by ventricular dilatation or inflammation, it is probably not repaired - Typical ependymal reactions to injury include a. Atrophy and reactive cell loss b. Formation of ependymaldiscontinuties c. subventriculargliosis (subventricularglial nodules)

  17. - Which appear as tiny clear granules(granular ependymitis) and best seen in the floor of the fourth ventricle.

  18. II.Edema, Hydrocephalus and Herniation

  19. A. Brain Edema -Is the accumulation of excess fluid within the brain parenchyma -There are two main types that may occur together mainly after generalized injury I. Vasogenic edema - Is the most common type - Affects mainly the white matter - Occurs when the integrity of the blood brain barrier

  20. is disrupted , allowing fluid to shift from the vascular compartment into the extracellular spaces of the brain and can be A. Localized in a. Brain tumors either primary or metastatic ( it is more severe in metastatic brain tumors) - In brain tumors, the blood vessels may be abnormal with fenestrations in the capillary wall b. Cerebral abscess

  21. Vasogenic edema surrounding glioblastoma

  22. B.. Generalized In late stages of ischemic encephalopathy due to damage of endothelial cells by ischemia II. Cytotoxic edema: - An increase in intracellular fluid secondary to neuronal or glial membrane injury - The extracellular space is reduced - The blood brain barrier is intact - Caused by ischemia to the brain

  23. - it occurs because energy failure disables the Na/K pump system allowing large amounts of sodium accompanied by water to enter the cells - Mainly affects the gray matter

  24. III. Interstitial Edema: - It occurs in Patients with acute obstructive high pressure hydrocephalus - Due to damage to the ependymal lining by stretching - Which leads to an increase in the water content in the periventricular white matter - It is most pronounced around the frontal and occipital horns of the lateral ventricles

  25. B. Hydrocephalus :- - Means accumulation of excessive CSF within the ventricular system as a result of a disturbance in its secretion, circulation or absorption a. Most commonly due to impaired flow or resorption of CSF b. Overproduction of CSF, seen in choroid plexus papilloma is only rarely causes hydrocephalus.

  26. Types of hydrocephalus I.Non-communicating hydrocephalus (obstructive): - It occurs when a lesion impedes the free passage of the CSF from the ventricles to the subarachnoid space, causing dilatation of the portion of the CSF pathway that lies proximal to the obstructions; Causes a. Obstructive hydrocephalus affecting the lateral ventricles only may be caused by colloid cyst of the third ventricle

  27. Or intraventricular hemorrhage or suprasellar tumors invaginating the anterior part of the third ventricle b. Obstruction of the posterior end of the third ventricle and aqueduct may be due to aqueductalstenosis or tumors of the pineal region c. Lesions obstructing the fourth ventricle such as ependymoma d. Lesions of the cerebellum such as medulloblastioma may produce sufficient distorsion of the the fourth ventricle

  28. e. Obstruction of the outlet of the fourth ventricle at level of formaina of Lushcka and Magendiemay result from acute inflammatory exudate related to meningitis, sarcoidosis II. Communicating hydrocephalus,: - Refers to the abnormality in which there is free passage of CSF from within the ventricular system into the subarachnoid space -Causes a. Defects in the subarachnoid space such as fibrosis in leptomeningeal infection and hemorrhage from saccular aneurysms

  29. B. Defects in absorption of CSF at the arachnoid granulations such as 1. congenital deficiency of arachnoids' granulation 2. Increased cerebral venous pressure C. Overproduction of CSF by choroid plexus papilloma D. Idiopathic

  30. QUIZ • MENTION NAMES OF THE LAYERS OF THE NEOCORTEX

More Related