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The different diagnoses of diseases and disorders within the nervous system are made using neuropathology in coordination with clinical signs/symptoms and imaging. The imaging techniques discussed in Chapter 9 , coalesced with biopsies, the use of selective antibodies to identify cellular markers, and particular stains to highlight cellular structures, are all used to make a diagnosis. This chapter will present some common neuropathological diseases/disorders.
Stains used to help identify the different cells of the central nervous system (CNS) include hematoxylin and eosin (H&E), Nissl stain, Luxol-fast blue stain, and silver stains. H&E stains are the most commonly used, with the cytoplasm of cells being more acidic (eosinophilic) and staining red, whereas the nuclei and nucleoli are more basic (hematoxylinophilic) and are stained blue. Nissl bodies, which are the rough endoplasmic reticulum of neurons, are basophilic, and the use of a Nissl stain (cresyl violet) results in a dark purple highlight of the rough endoplasmic reticulum. Axons and dendrites cannot be distinguished unless there are swelling-related changes. Astrocytes lack an eosinophilic cytoplasm and have nuclei that appear large and quite clear. When astrocytes react to tissue damage, they appear eosinophilic because their cytoplasm becomes more abundant as a result of an increase in fibrous components, which also accumulate in the nerve processes. Oligodendroglia are smaller than astrocytes, with basophilic densely staining nuclei and a barely visible cytoplasm. The nuclei of microglia present with basophilic club-shaped terminations and are thus easily distinguished. Luxol-fast blue stains the myelin sheath (lipids) blue and is often used to help diagnose demyelinating diseases.
Silver stains (i.e., Bodian staining) use silver, copper, and gold to stain neuronal cell bodies and nerve processes dark brown. Parts of the cells that take up the “silver” stain (called argentaffin parts) can include areas of localized axonal swelling, dendritic lesions, and Alzheimer neurofibrillary degeneration (neurofibrillary tangles [NFTs]). Other silver staining procedures enable clear visualization of amyloid components of senile plaques; immunostained images of β-amyloid proteins show similar results.
Tumors of the brain include astrocytomas, oligodendrogliomas, and ependymomas, medulloblastomas as well as several others. Originally these primary brain tumors were thought to originate from glial cells, hence the name (gliomas); recent evidence suggest that they may not only come from glial cells but also from neural stem cells and are characterized based on the expression of particular cell markers. Primary brain tumors are classified not only using stains, selective antibodies, and/or their location (i.e., intra-axial = within the brain parenchyma, or extra-axial = outside of the brain parenchyma) but also based on how well defined the borders of the tumor are (i.e., well circumscribed vs. diffuse). In addition, there are tests, such as KI67 staining for identifying mitotic activity, performed in order to detect how rapidly the cancer is dividing, and the majority of tumors are given a “grade” (grades I-IV from slow to fast) for growth aggressiveness.
Astrocytomas are thought to develop from astrocytes and may arise anywhere in the brain or spinal cord (intra-axial), yet they most often occur in the cerebrum. Astrocytomas are the most common primary CNS tumors and can be further divided based on their ability to either remain localized or diffusely infiltrate.
Infiltrating astrocytomas are the most common adult primary CNS (intra-axial) tumor; they are often found in the cerebrum but can also appear in the cerebellum, brainstem, and spinal cord. These types of tumors can range from diffuse astrocytoma (grade II), to anaplastic astrocytoma (grade III), to glioblastoma (grade IV), depending on markers and their speed of proliferation (tumor aggression).
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