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XXIII - The Nervous System Flashcards

1
Q

This pattern of neuronal cell injury leads to shrunken individual cell bodies and nuclei. They are prominently stained by eosin, leading to the term “red neurons.” SEE SLIDE 23.1.

A

Acute hypoxic/ischemic injury(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 860

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2
Q

These are round, faintly basophilic, PAS-positive, concentrically lamellated aggregates of polyglucosans that range between 5 and 50 micrometers, and are located wherever there are astrocytic end processes, especially in the subpial and perivascular zones, seen more frequently with advancing age. SEE SLIDE 23.2.

A

Corpora amylacea (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 861

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3
Q

Cells which produce myelin in the CNS.

A

Oligodendrocytes (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 861

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4
Q

Cells which line the ventricles, and are located in the region of the obliterated central canal of the spinal cord.

A

Ependymal cells (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 861

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5
Q

These are responsible for the secretion of CSF. It has a specialized epithelial covering with a fibrovascular stroma that may contain meningothelial cells.

A

Choroid plexus (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 861

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6
Q

These are bone marrow-derived cells that function as the phagocytes of the CNS.

A

Microglia (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 861

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7
Q

It is the accumulation of excess fluid within the brain parenchyma. The brain is softer than normal and often appears to “overfill” the cranial vault. In generalized edema the gyri are flattened, the intervening sulci are narrowed, and the ventricular cavities are compressed.

A

Cerebral Edema (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 861

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8
Q

This occurs when the integrity of the normal blood-brain barrier is disrupted. With increased vascular permeability, fluid shifts from the vascular compartment into the intercellular spaces of the brain.

A

Vasogenic edema (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 861

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9
Q

This is due to an increase in intracellular fluid secondary to neuronal, glial, or endothelial cell membrane injury, as might be encountered in an individual with a generalized hypoxic/ischemic insult or with exposure to some toxins.

A

Cytotoxic edema(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 861

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10
Q

Refers to the accumulation of CSF leading to dilation of the ventricular system which resulted from an obstacle or disruption of flow seen most commonly at the foramen of Monroe or aqueduct of Sylvius.

A

Noncommunicating hydrocephalus (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 862

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11
Q

Refers to the accumulation of CSF leading to dilation of the ventricular system due to reduced resorption of CSF. All of the ventricular system is enlarged.

A

Communicating hydrocephalus (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 862

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12
Q

This refers to dilation of the ventricular system with a compensatory increase in CSF volume secondary to a loss of brain parenchyma, as may occur after infarcts or with a degenerative disease.

A

Hydrocephalus ex vacuo (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 862

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13
Q

This ccurs when unilateral or asymmetric expansion of a cerebral hemisphere displaces the cingulate gyrus under the edge of falx. This may be associated with compression of branches of the anterior cerebral artery.

A

Subfalcine (cingulate) herniation(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 862

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14
Q

This occurs when the medial aspect of the temporal lobe is compressed against the free margin of the tentorium. As the temporal lobe is displaced, the third cranial nerve is compromised, resulting in pupillary dilation and impairment of ocular movements on the side of the lesion (“blown pupil”).

A

Transtentorial (uncinate) herniation (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 862

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15
Q

This refers to displacement of the cerebellar tonsils through the foramen magnum. This pattern of herniation is life-threatening, because it causes brain stem compression and compromises vital respiratory and cardiac centers in the medulla.

A

Tonsillar herniation (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 862

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16
Q

These linear or flame-shaped lesions usually occur in the midline and paramedian regions, which are hemorrhagic lesions that accompany transtentorial herniation. Presence of these lesion implies poor prognosis.

A

Duret hemorrhages(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 862

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17
Q

In the setting of this condition, the brain is swollen, with wide gyri and narrowed sulci. The cut surface shows poor demarcation between gray and white matter. Results from generalized reduction of cerebral perfusion, usually below systolic pressures of less than 50mmHg.

A

Global Cerebral Ischemia (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 863

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18
Q

These are wedge-shaped areas of infarction that occur in those regions of the brain and spinal cord that lie at the most distal fields of arterial perfusion. Usually seen after hypotensive episodes.

A

Border zone (“watershed”) infarcts. Most at risk: border zone between anterior and middle cerebral artery. (TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1264

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19
Q

Pattern of necrosis seen in nonhemorrhagic infarcts of the brain.

A

Liquefaction necrosis(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 863

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20
Q

The most frequent cause of subarachnoid hemorrhage. It is a thin-walled outpouching of an artery. At the neck of the aneurysm, the muscular wall and intimal elastic lamina stop short and are absent from the aneurysm sac itself; the sac is made up of thickened hyalinized intima. The adventitia covering the sac is continuous with that of the parent artery

A

Saccular (berry) aneurysm(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 866

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21
Q

Patients with this type of intracranial hemorrhage complains of having “the worst headache I’ve ever had”/ thunderclap headache.

A

Subarachnoid Hemorrhage (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 866

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22
Q

Most common location for berry/saccular aneurysms.

A

Anterior communicating artery in the Circle of WIllis (40%)(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 867

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23
Q

This is a disease in which amyloidogenic peptides are deposit in the walls of medium- and small-caliber meningeal and cortical vessels, which results in the weakening of the vessel wall and increases the risk of hemorrhage.

A

Cerebral amyloid angiopathy (CAA) (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 863

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24
Q

Hemorrhages associated with cerebral amyloid angiopathy (CAA) due to involvement of the cerebral hemispheres?

A

Lobar hemorrhages(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 863

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25
Q

A type of vascular malformation which are characterized by of ectatic venous channels.

A

Venous angiomas (varices) (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 868

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26
Q

Most common location for berry aneurysms.

A

Anterior communicating artery in the Circle of WIllis (40%)(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 867

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27
Q

The involved vessels in this condition resemble a tangled network of wormlike vascular channels. Microscopically, they are enlarged blood vessels separated by gliotic tissue, often with evidence of prior hemorrhage.

A

Arteriovenous malformations (AVM)(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 868

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28
Q

A type of vascular malformation which are characterized by microscopic foci of dilated, thin-walled vascular channels separated by relatively normal brain parenchyma and occurring most frequently in the pons.

A

Capillary telangiectasias(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 868

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29
Q

Minute aneurysms in vessels that are less than 300 micrometers in diameter, associated with chronic hypertension.

A

Charcot-Bouchard microaneurysms (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 868

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30
Q

This leads to accumulation of arterial blood between the dura and the skull. The expanding hematoma has a smooth inner contour that compresses the brain surface. Clinically, patients may experience a lucid interval between the moment of trauma and development of neurologic symptoms.

A

Epidural Hematoma. SEE SLIDE 23.3. (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 870

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31
Q

This is an inflammatory disorder that involves multiple small to medium-sized parenchymal and subarachnoid vessels and is characterized by chronic inflammation, multinucleated giant cells and destruction of the vessel wall. Affected individuals manifest a diffuse encephalopathic clinical picture, often with cognitive dysfunction; improvement occurs with steroid and immunosuppressive treatment.

A

Primary angiitis of the CNS (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 868

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32
Q

This describes reversible altered consciousness from head injury in the absence of contusion. The characteristic transient neurologic dysfunction includes loss of consciousness, temporary respiratory arrest, and loss of reflexes.

A

Concussion(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 869

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33
Q

Injury which may occur from collision of the brain with the skull opposite the site of impact.

A

Contrecoup injury(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 868

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34
Q

These are wedge shaped lesions of the brain parenchyma which occur secondary to trauma. The broad base of the wedge spans the surface and centered on the point of impact.

A

Contusions(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 868

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35
Q

Blood vessel involved in epidural hematoma.

A

Middle meningeal artery(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 870

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36
Q

Blood vessels involved in subdural hemorrhage.

A

Bridging veins(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 870

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37
Q

This is an extension of CNS tissue through a defect in the vertebral column, most commonly in the lumbosacral region. both The meninges and spinal cord parenchyma are included in the cystlike structure visible just above the buttocks.

A

Myelomeningocele. SEE SLIDE 23.4. (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 872

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38
Q

Herniation of the meninges through a defect in the vertebral column.

A

Meningocoele. SEE SLIDE 23.4. (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 872

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39
Q

This is a malformation of the anterior end of the neural tube, with absence of the brain and top of skull.

A

Anencephaly. SEE SLIDE 23.5. (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 872

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40
Q

This is a diverticulum of malformed CNS tissue extending through a defect in the cranium. It most often involves the occipital region or the posterior fossa.

A

Encephalocele. SEE SLIDE 23.5. (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 872

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41
Q

Characterized by an increased number of irregularly formed gyri that result in an irregular bumpy or cobblestone-like surface.

A

Polymicrogyria(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 872

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42
Q

Characterized by a disruption of the normal midline patterning. In severe forms the brain is not divided into hemispheres or lobes and may be associated with facial midline defects like cyclopia.

A

Holoprosencephaly (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 872

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43
Q

Consists of a small posterior fossa and a misshapen midline cerebellum with downward extension of vermis through the foramen magnum; hydrocephalus and a lumbar myelomeningocele are typically also present.

A

Arnold-Chiari malformation Type II(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 872

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44
Q

Consists of low-lying cerebellar tonsils which extend through the foramen magnum at the base of the skull. This can lead to obstruction of CSF flow and compression of the medulla, resulting in symptoms of headache or cranial nerve deficits.

A

Arnold-Chiari malformation type I(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 872

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45
Q

Cerebral malformation characterized by an enlarged posterior fossa. The cerebellar vermis is absent, and replaced by a large, midline cyst that is lined by ependyma and is contiguous with leptomeninges on its outer surface. SEE SLIDE 23.6.

A

Dandy-Walker malformation (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 872

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46
Q

Spinal cord abnormality characterized by a discontinuous or confluent expansion of the ependyma-lined central canal of the cord.

A

Hydromyelia(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 873

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47
Q

CSF findings in bacterial meningitis.

A

Increased pressureabundant neurophilsprotein - elevatedglucose - reduced(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 874

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48
Q

This is an inflammatory process of the leptomeninges and CSF within the subarachnoid space.

A

Meningitis (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 874

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49
Q

In acute cases of this condition, an exudate is evident within the leptomeninges over the surface of the brain. On microscopic examination, neutrophils fill the entire subarachnoid space in severely affected areas or may be found predominantly around the leptomeningeal blood vessels.

A

Acute meningitis(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 874

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50
Q

A form of neurosyphilis, resulting from damage to the sensory nerves in the dorsal roots producing impaired joint position sense and resultant ataxia, loss of pain sensation, leading to skin and “Charcot joints” (deformed bones). There is loss of both axons and myelin in the dorsal roots, with pallor and atrophy in the dorsal columns of the spinal cord.

A

Tabes dorsalis (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 875

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51
Q

Presents with generalized symptoms of headache, malaise, mental confusion, and vomiting. The subarachnoid space contains a gelatinous or fibrinous exudate, most often at the base of the brain, obliterating the cisterns and encasing cranial nerves. There may be discrete white granules scattered over the leptomeninges. Obliterative endarteritis may be seen.

A

Tuberculous meningitis (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 874

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52
Q

CSF findings in tuberculous meningitis.

A

Moderate pleiocytosis - predominantly monocytesprotein - elevatedglucose - moderately reduced/normal(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 874

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53
Q

Caused by invasion of the brain by Treponema pallidum and manifests as insidious but progressive loss of mental and physical functions with mood alterations (including delusions of grandeur), terminating in severe dementia.

A

Paretic neurosyphilis (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 874

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54
Q

This virus tends to localize in the paraventricular subependymal regions of the brain, which results in a severe hemorrhagic necrotizing ventriculoencephalitis and choroid plexitis.

A

Cytomegalovirus (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 877

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55
Q

These are discrete lesions with central liquefactive necrosis and a surrounding fibrous capsule. On microscopic examination, there is exuberant neovascularization around the necrosis that is responsible for the marked edema and formation of granulation tissue. Outside the fibrous capsule is a zone of reactive gliosis.

A

Brain Abscesses (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 876

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56
Q

The pathognomonic finding of this disease is a spongiform transformation of the cerebral cortex and deep gray matter structures (caudate, putamen); consists of a multifocal process that results in the uneven formation of small, empty, microscopic vacuoles of varying sizes within the neuropil and sometimes in the perikaryon of neurons. SEE SLIDE 23.7.

A

Creutzfeldt-Jakob Disease (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 880

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57
Q

Viral encephalitis which involves inferior and medial regions of the temporal lobes and the orbital gyri of the frontal lobes. Perivascular inflammatory infiltrates are usually present, and Cowdry type A intranuclear viral inclusion bodies can be found in both neurons and glia. SEE SLIDE 23.8.

A

Herpes Encephalitis(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 876

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58
Q

Reactivation of varicella in adults manifests as a painful, vesicular skin eruption in the distribution of one or a few dermatomes.

A

Shingles / Herpes Zoster(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 876

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59
Q

This lesion caused by JC virus, consist of patches of irregular, ill-defined destruction of the white matter that enlarge. Each lesion is an area of demyelination, in the center of which are scattered lipid-laden macrophages and a reduced number of axons.

A

Progressive Multifocal Leukoencephalopathy (PML) (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 877

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60
Q

These are predominantly benign tumors of adults, usually attached to the dura, and arising from the meningothelial cell of the arachnoid. Histologic patterns include syncitial, fibroblastic, psammomatous (SEE SLIDE 23.9), secretory and microcystic.

A

Meningiomas(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 885

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61
Q

Five most common primary sites of carcinoma which may metastasize to the brain.

A

LungBreastSkin (melanoma)KidneyGIT(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 885

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62
Q

These are infiltrative tumors that form gelatinous, gray masses, and may show cysts, focal hemorrhage, and calcification. On microscopic examination, the tumor is composed of sheets of regular cells with spherical nuclei containing finely granular chromatin (similar to normal oligodendrocytes) surrounded by a clear halo of cytoplasm. SEE SLIDE 23.10

A

Oligodendrogliomas(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 883

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63
Q

A nonimmune process characterized by loss of myelin involving the center of the pons, most often after rapid correction of hyponatremia.

A

Central pontine myelinolysis (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 889

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64
Q

These are inherited dysmyelinating diseases in which the clinical symptoms derive from either abnormal myelin synthesis or turnover.

A

Leukodystrophies (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 889

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65
Q

Profound memory disturbances as a result of thiamine deficiency.

A

Korsakoff syndrome(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 890

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66
Q

An autoimmune demyelinating disorder characterized by distinct episodes of neurologic deficits, separated in time, attributable to white matter lesions that are separated in space. Affected areas show multiple, well-circumscribed, slightly depressed, glassy, gray-tan, irregularly shaped lesions, termed “plaques”.

A

Multiple Sclerosis (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 887

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67
Q

This condition occurs in the setting of thiamine deficiency and chronic alcoholism. Characterized by foci of hemorrhage and necrosis, particularly in the mammillary bodies but also adjacent to the ventricle, especially the third and fourth ventricles.

A

Wernicke encephalopathy(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 890

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68
Q

Characterized by “flapping” tremor, depressed levels of consciousness, which may lead to coma. Result of decreased hepatic function.

A

Hepatic encephalopathy (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 891

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69
Q

It is the most common cause of dementia in the elderly, characterized by presence of plaques and neurofibrillary tangles, composed of tau proteins. SEE SLIDE 23.11.

A

Alzheimer’s disease(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 893

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70
Q

Mutation in Friedreich ataxia.

A

GAA trinucleotide repeat (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 895

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71
Q

This is a clinical syndrome characterized by masked facies, stooped posture, slowness of voluntary movement, festinating gait rigidity, and a “pill-rolling” tremor. There are single or multiple, intracytoplasmic, eosinophilic, round to elongated inclusions that often have a dense core surrounded by a pale halo or “Lewy bodies”. SEE SLIDE 23.12.

A

Parkinson disease (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 894

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72
Q

It is an inherited autosomal dominant disease characterized clinically by progressive movement disorders and dementia, with degeneration of the striatum (caudate and putamen).

A

Huntington Disease (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 894

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73
Q

Mutation in Huntington disease.

A

CAG trinucleotide repeats(TOPNOTCH)Robbins Basic Pathology, 8th ed., p 895

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74
Q

It is an autosomal recessive progressive illness, generally beginning in the first decade of life with gait ataxia, followed by hand clumsiness and dysarthria.

A

Friedreich ataxia (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 895

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75
Q

This is the most common form of neurodegeneration affecting the motor system. It is characterized by muscle atrophy and hypereflexia due to loss of both upper and lower motor neurons.

A

Amyotrophic Lateral Sclerosis (Motor Neuron Disease; Lou Gehrig’s Disease) (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 895

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76
Q

This is one of the most common life-threatening diseases of the peripheral nervous system. It may develop spontaneously or after a systemic infection (usually viral) or other stress. Usually presents with rapidly progressive, ascending motor weakness that may lead to death from failure of respiratory muscles.

A

Guillain-Barre Syndrome (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 899

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77
Q

These are benign tumors arising from Schwann cells, which are well-circumscribed encapsulated, firm, gray masses but may also have areas of cystic and xanthomatous change.

A

Schwannomas (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 899

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78
Q

Present in the dermis and subcutaneous fat, these well-delineated but unencapsulated masses are composed of spindle cells. The stroma of these tumors is highly collagenized and contains little myxoid material.

A

Cutaneous neurofibroma. SEE SLIDE 23.13. (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 899

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79
Q

These tumors may arise anywhere along a nerve, may be multiple, and is not easily separated from the nerve.

A

Plexiform neurofibroma. SEE SLIDE 23.13. (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 899

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80
Q

This autosomal dominant disorder is characterized by neurofibromas (plexiform and solitary), gliomas of the optic nerve, pigmented nodules of the iris (Lisch nodules), and cutaneous hyperpigmented macules (cafe au lait spots).

A

Type 1 Neurofibromatosis (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 901

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81
Q

This is an autosomal dominant disorder in which patients develop a range of tumors, most commonly bilateral vestibular (acoustic) schwannomas and multiple meningiomas.

A

Type 2 Neurofibromatosis (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 901

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82
Q

An autosomal dominant syndrome characterized by the development of hamartomas and benign neoplasms involving the brain and other tissues. The lesions are firm areas of the cortex that, in contrast to the softer adjacent cortex, have been likened to potatoes, hence the appellation “tubers.” SEE SLIDE 23.14.

A

Tuberous Sclerosis (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 901

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83
Q

An autosomal dominant inherited disease in characterized by development of hemangioblastomas within the cerebellar hemispheres, retina, and less commonly the brain stem and spinal cord. A cerebellar capillary hemangioblastoma, is the principal neurologic manifestation of the disease.

A

von Hippel-Lindau Disease (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 901

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84
Q

What is the dominant histopathologic finding in Immune mediated neuropathies like Guillain- Barre Syndrome?

A

Inflammation of peripheral nerve, manifested as perivenular and endoneurial infiltration by lymphocytes, macrophages, and a few plasma cells. SEE SLIDE 23.15. (TOPNOTCH)

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85
Q

What is the most common type of peripheral neuropathy seen in adult-onset DM?

A

Symmetric neuropathy that involves distal sensory and motor nerves (TOPNOTCH)

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86
Q

In patients with peripheral neuropathy, what is the predominant histologic findings?

A

Axonal neuropathy (TOPNOTCH)

87
Q

Morphology: Perifascicular Atrophy

A

Dermatomyositis. SEE SLIDE 23.16. (TOPNOTCH)

88
Q

Morphology: presence of rimmed vacuoles within myocytes and are highlighted by basophilic granules at their periphery. In addition, the vacuolated fibers may also contain amyloid deposits that stain with Congo Red.

A

Inclusion body myositis (TOPNOTCH)

89
Q

Morphology: Panfascicular atrophy

A

Spinal Muscular Atrophy (Infantile Motor Neuron Disease. SEE SLIDE 23.17. (TOPNOTCH)

90
Q

What are the 5 histopathologic abnormalities common to Duchenne Muscular Dystrophy and Becker Muscular Dystrophy?

A
  1. Variation in fiber diameter 2. Increased numbers of internalized nuclei 3. Degeneration, necrosis, and phagocytosis of muscle fibers 4. Regeneration of muscle fibers 5. Proliferation of endomysial connective tissue. SEE SLIDE 23.18 (TOPNOTCH)
91
Q

Morphology: In later stages of this disease, all muscles eventually become almost totally replaced by fat and connective tissue

A

Duchenne Muscle Dystrophy (TOPNOTCH)

92
Q

What is the histologic pathology that is usually seen in Duchene muscle dystrophy and is rare in Becker Muscle Dystrophy?

A

Enlarged, rounded, hyaline fibers that have lost their normal cross striation, believed to be hypercontracted fibers (TOPNOTCH)

93
Q

Morphology: Ring fiber ( subsarcolemmal band of cytoplasm that appears distinct from the center of the fiber) and Sarcoplasmic mass

A

Myotonic Dystrophy. SEE SLIDE 23.19 (TOPNOTCH)

94
Q

Morphology: Disuse changes with Type 2 fiber atrophy, post synaptic membrane is simplified, with loss of AChRs from the region of the synapse. Immune complexes as well as the MAC of the complement cascade can be found along the post synaptic membrane as well

A

Myasthenia Gravis (TOPNOTCH)

95
Q

Electron Microscopy: tubular and filamentous inclusions are seen in the cytoplasm and the nucleus, and they are composed of B-amyloid or hyperphosphorylated tau.

A

Inclusion body myositis (TOPNOTCH)

96
Q

Grotton lesions (scaling erythematous eruption or dusky red patches over the knuckles, elbows, and knees) are seen in what disease entity? SEE SLIDE 23.20.

A

Dermatomyositis (TOPNOTCH)

97
Q

Morphology: the most consistent pathologic findings in skeletal muscle are aggregates of abnormal mitochondria that stain with modified Gomori Trichrome and fiber appears irregular on cross section “ragged red fibers” and on electron microscope, they contain “parking lot inclusions” SEE SLIDE 23.21.

A

Mitochondrial Myopathies (Oxidative phosphorylation Disease) (TOPNOTCH)

98
Q

This is general reaction of the motor unit which is a result of primary destruction of the axon, with secondary disintegration of its myelin sheath.

A

Axonal degeneration (TOPNOTCH)

99
Q

This general reaction of the motor unit occurs when there is dysfunction of the Schwann cell or damage to the myelin sheath; there is no primary abnormality of the axon

A

Segmental demyelination (TOPNOTCH)

100
Q

Morphology: Endoneurial arterioles show thickening, hyalinization, and intense PAS positivity in their walls and extensive reduplicaton of the basement membrane. SEE SLIDE 23.22

A

Peripheral Neuropathy in DM Type 2 (TOPNOTCH)

101
Q

Of all the dystrophies, this type is the only one that shows pathologic changes in the intrafusal fibers of muscle spindles, with fiber splitting, necrosis and regeneration.

A

Myotonic Dystrophy (TOPNOTCH)

102
Q

Morphology: the principal morphologic characteristic is accumulation of lipid within myocytes. The myofibrils are separated by vacuoles that stain with oil red O or Sudan black

A

Lipid Myopathies (TOPNOTCH)

103
Q

Lambert Eaton Myasthenic Syndrome is a paraneoplastic process which commonly develops in what type of carcinoma?

A

Small cell carcinoma of the lungs (TOPNOTCH)

104
Q

The most important histopathological indicator of CNS injury, regardless of etiology

A

Gliosis(TOPNOTCH)

105
Q

Lafora bodies

A

Myoclonic Epilepsy(TOPNOTCH)

106
Q

A syndrome of sudden, deep intracerebral hemorrhage that follows even minor head trauma by an interval of 1-2 weeks

A

Spat-apoplexie (Delayed post traumatic hemorrhage) (TOPNOTCH)

107
Q

Subdural hematomas most often become manifest approximately how many hours after the injury?

A

48 hours(TOPNOTCH)

108
Q

The most widely accepted explanation for diffuse axonal injury

A

mechanical forces damage the integrity of the axon at the node of Ranvier, with subsequent alterations in axoplasmic flow(TOPNOTCH)

109
Q

Morphology: wide asymmetric distribution of axonal swellings that appear within hours of the injury and are best demonstrated with silver impregnation techniques or with immunoperoxidase stains for AB protein

A

Diffuse axonal injury(TOPNOTCH)

110
Q

How long does it take for the clot to lyse in subdural hematomas?

A

1 week(TOPNOTCH)

111
Q

How long does it take for fibroblasts to grow from the dural surfaces into the hematoma after subdural hematoma/

A

2 weeks(TOPNOTCH)

112
Q

How long does it take for the development hyalinized connectice tissue in SDH

A

1-3 months(TOPNOTCH)

113
Q

In the setting of global ischemia, early histological changes are seen after how many hours after the insult?

A

12-24 hours(TOPNOTCH)

114
Q

In the setting of global ischemia, subacute changes are seen after how many hours after the insult?

A

24 hours to 2 weeks(TOPNOTCH)

115
Q

In the setting of global cerebral ischemia, repair is seen after approximately how many weeks?

A

2 weeks(TOPNOTCH)

116
Q

In the setting of global ischemia, this is characterized by eventual removal of all necrotic tissue, loss of normally organized CNS structure, and gliosis

A

Repair(TOPNOTCH)

117
Q

In the setting of global ischemia, this is characterized by necrosis of tissue, influx of macrophages, vascular proliferation and reactive gliosis

A

Subacute changes(TOPNOTCH)

118
Q

In the setting of global ischemiaThis is characterized by acute neuronal cell damage

A

Early change(TOPNOTCH)

119
Q

Morphology: Mononuclear cell perivacular cuffs and neuronophagia of the anterior horn motor neurons of the spinal cord. SEE SLIDE 23.23.

A

Poliomyelitis(TOPNOTCH)

120
Q

In the immunosuprressed individual, the most common pattern of involvement in viral meningitis is:

A

Subacute encephalitis(TOPNOTCH)

121
Q

Although any type of cell within the CNS can be infected with CMV, the virus tends to localize at what particular area in the brain?

A

Paraventricular subependymal regions(TOPNOTCH)

122
Q

What is the principal neurologic manifestation of Von Hippel Lindau Disease?

A

Cerebellar capillary hemangioblastoma(TOPNOTCH)

123
Q

Antoni A and Antoni B patterns of growth are seen in what tumors of the CNS? SEE SLIDE 23.24.

A

Schwannoma. In Antoni A areas, cells align to produce nuclear palisading, with alternating bands of nuclear and anuclear areas called VEROCAY BODIES. (TOPNOTCH) Robbins Basic Pathology, 9th ed, p 807.

124
Q

Morphology: Histologic appearance similar to anaplastic astrocytoma with the additional feature of necrosis and vascular or endothelial cell proliferation. SEE SLIDE 23.25

A

Glioblastoma multiforme(TOPNOTCH)

125
Q

Pseudopalisading. SEE SLIDE 23.25

A

Glioblastoma multiforme(TOPNOTCH)

126
Q

Glomeruloid body

A

Glioblastoma multiforme(TOPNOTCH)

127
Q

Lesion of what area of the brain appear to be the best correlate of the memory disturbance and confabulation seen in Korsakoff syndrome?

A

Medial dorsal nucleus of the thalamus(TOPNOTCH)

128
Q

The spinal cord shows loss of axons and gliosis in the posterior columns, the distal portions of the corticospinal tracts, and the spinocerebellar tracts.

A

Friedreich Ataxia(TOPNOTCH)

129
Q

The abnormalities are predominantly in the cerebellum,with loss of Purkinje and granule cells; there is also degeneration of the dorsal columns, spinocerebellar tracts and anterior horn cells and a peripheral neuropathy

A

Ataxia Telangiectasia(TOPNOTCH)

130
Q

Gross morphology: pallor of the substantia nigra and locus ceruleus

A

Parkinson Disease(TOPNOTCH)

131
Q

Gross morphology: the brain shows pronounced, frequently asymmetric, atrophy of the frontal and temporal lobes with conspicuous sparing of the posterior two thirds of the superior temporal gyrus

A

Pick Disease(TOPNOTCH)

132
Q

What are the 3 major microscopic abnormalities of Alzheimer disease?

A

Neuritic/Senile PlaquesNeurofibrillary tanglesAmyloid angiopathy. SEE SLIDE 23.11. (TOPNOTCH)

133
Q

What is the principal clinical manifestation of Alzheimer disease?

A

Dementia(TOPNOTCH)

134
Q

What is the most common cause of dementia in the elderly?

A

Alzheimer Disease(TOPNOTCH)

135
Q

Gross morphology: Variable degree of cortical atrophy with widening of the cerebral sulci that is most pronounced in the frontal, temporal, and parietal lobes with compensatory ventricular enlargement (hydrocephalus ex vacuo)

A

Alzheimer Disease(TOPNOTCH)

136
Q

Neurotic plaques are focal, spherical collection of dilated, tortuous, silver staining neuritic processes often around a central amyloid core, which may be surrounded by clear halo, and can be stained with Congo red. SEE SLIDE 23.11. What is the most predominant component of this plaque core?

A

AB peptide(TOPNOTCH)

137
Q

Neurofibrillary tangles are bundles of filaments in the cytoplasm of the neurons that displace or encircle the nucleus. SEE SLIDE 23.11. What is the major component of this structure?

A

Tau proteins(TOPNOTCH)

138
Q

Hirano bodies. SEE SLIDE 23.11

A

Alzheimer’s disease (TOPNOTCH)

139
Q

What is the principal neurologic manifestation of Von Hippel Lindau Disease?

A

Cerebellar capillary hemangioblastoma(TOPNOTCH)

140
Q

Patients with Von Hippel Lindau Disease has the propensity to develop what type of carcinom?

A

Renal Cell Carcinoma(TOPNOTCH)

141
Q

These are firm areas of the cortex that, in contrast to the softer adjacent cortex, have been likened to potatoes and are composed of haphazardly arranged neurons that lack the normal laminar organization of neocortex.

A

Cortical hamartomas or “tubers’ of Tuberous Sclerosis (TOPNOTCH)

142
Q

Malignant Peripheral Nerve Sheath Tumor (MPNST, Malignant Schwannoma) is strongly associated with what type of Familial Tumor Syndrome?

A

Neurofibromatosis Type 1(TOPNOTCH)

143
Q

What are the 5 most common carcinoma that metastasize to the brain?

A

Lung, breast, Melanoma, Kidney, and GIT. (TOPNOTCH)

144
Q

What is the most common CNS neoplasm in immunosuppressed patients, including those with AIDS and immunosuppression after transplantaion?

A

Primary CNS Lymphoma(TOPNOTCH)

145
Q

Morphology: Characterized by amild to moderate increase in the number of glial cell nuclei, somewhat variable nuclear pleomorphism, and an interveing feltwork of fine, GFAP positive astrocytic cell processes that give the background a fibrillary appearance.

A

Well differentiated fibrillary astrocytomas(TOPNOTCH)

146
Q

Morphology: Perivascular pseudorosettes SEE SLIDE 23.26

A

Ependymoma(TOPNOTCH)

147
Q

Morphology: The anterior roots of the spinal cord are thin; the precentral gyrus may be atrophic and demonstrates a reduction the number of anterior horn neurons throughout the length of the spinal cord with associated reactive gliosis. Remaining neurons often contain Bunina bdoies and PAS positive cytoplasmic inclusions.

A

Amyotorphic Lateral Sclerosis(TOPNOTCH)

148
Q

Morphology: composed of bipolar cells with long, thin “hairlike” processes that are GFAP- Positive; Rosenthal fibers, eosinophilic granular bodies, and microcysts are often present. SEE SLIDE 23.27.

A

Pilocytic Astrocytoma (TOPNOTCH)

149
Q

Morphology: Characterized by areas of stromal response with collagen and reticulin deposition and nodules of cells forming “pale islands” that have more neuropil and lack the reticulin deposition

A

Desmoplastic variant of Medulloblastoma(TOPNOTCH)

150
Q

Gross morphology: the brain is small and shows striking atrophy of the caudate nucleus and the putamen. The globus pallidus may be atrophied secondarily, and the lateral and third ventricles are dilated.

A

Huntington Disease(TOPNOTCH)

151
Q

What are the two most common primary tumors of the optic nerve?

A

Glioma and Meningioma (TOPNOTCH)

152
Q

Morphology: characterized histologically by chronic inflammation and replacement of orbital fat by fibrosis

A

Idiopathic orbital inflammation (TOPNOTCH)

153
Q

What is the most common malignancy of the eyelid?

A

Basal cell carcinoma (TOPNOTCH)

154
Q

Morphology: histological hallmark is the thinning of the cornea with breaks in the Bowman’s layer

A

Keratoconus (TOPNOTCH)

155
Q

Morphology: deposition of calcium in Bowmans layer

A

Calcific Band keratopathy (TOPNOTCH)

156
Q

This type of keratopathy develops in patients who are exposed chronically to high levels of ultraviolet light

A

Actinic band keratopathy (TOPNOTCH)

157
Q

Morphology: numerous drop like excrescences - guttata- protrude downward from Descemet’s membrane

A

Fuchs dystrophy (TOPNOTCH)

158
Q

Also known as the End-Stage Eye

A

Phthisis Bulbi (TOPNOTCH)

159
Q

Morphology: diffuse loss of ganglion cells and thinning of the retinal nerve fiber layer, in advanced cases, the optic nerve is both cupped and atrophic

A

Glaucomatous optic nerve damage (TOPNOTCH)

160
Q

Flexner Wintersteiner Rosettes

A

Retinoblastoma (TOPNOTCH)

161
Q

Morphology: A neovascular membrane is positioned between the retinal pigment epithelium and Bruchs membrane

A

Age related macular degeneration (TOPNOTCH)

162
Q

“Waxy pallor” of the optic disk. SEE SLIDE 23.28

A

Retinitis Pigmentosa (TOPNOTCH)

163
Q

In this condition, both rods and cones are lost to apoptosis

A

Retinitis Pigmentosa (TOPNOTCH)

164
Q

Elschnig’ spots

A

Malignant hypertension (TOPNOTCH)

165
Q

What is known to be a reliable histological marker of diabetes mellitus in the eye?

A

Thickening of the BM of the epithelium of the pars plicata of the ciliary body (TOPNOTCH)

166
Q

Cytoid bodies

A

Hypertension (TOPNOTCH)

167
Q

Macular star

A

Malignant hypertension (TOPNOTCH)

168
Q

Morphology: Characterized by diffuse granulomatous inflammation of the urea. Plasma cells are typically absent, but eosiophils may be identified in the infiltrate

A

Sympathetic ophthalmia (TOPNOTCH)

169
Q

What is the most common intraocular malignancy in adults?

A

Metastasis to the uvea, typically to the choroid (TOPNOTCH)

170
Q

What is the most common primary intraocular malignancy in adults?

A

Uveal melanoma (TOPNOTCH)

171
Q

These are the resident monocyte-lineage population of CNS that proliferate and accumulate in response to injury.

A

Microglia (TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1254

172
Q

Subfalcine(cingulate) herniation leads to compression of what blood vessel?

A

Anterior cerebral artery(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1255

173
Q

Transtentoria(uncinate) herniation compress what structures?

A

CN III and Posterior Cerebral artery(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1255

174
Q

Patient X who had a moderate traumatic injury presented with lethargy. 12 hours later it he progressed rapidly to having dilated pupils and impairment of ocular movements. This is most likely due to:

A

Transtentorial (uncinate) herniation/CN III compression (TOPNOTCH)

175
Q

A malformation characterized by reduction in the number of gyri, agyria in extreme cases

A

Lissencephaly(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1257

176
Q

Infarcts in the supratentorial periventricular white matter in premature infants presenting with chalky yellow plaques consisting of discrete regions of white matter necrosis and calcification

A

Perventricular leukomalacia(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1259

177
Q

Most common site of contusions in the brain

A

Frontal and temporal lobes(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1260

178
Q

Vascular injury presenting with slowly evolving neurologic symptoms, often with a delay from the time of injury(most often within 48 hours of injury) Grossly, it appears as a collection of freshly clotted blood along the brain surface, without extension into the depths of sulci.

A

Subdural hematoma(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1262

179
Q

After a vehicular crash, patient presented with quadriplegia and respiratory distress. Spinal cord injury was suspected. This can be due to damage to what level of vertebra?

A

Above C4(TOPNOTCH)

180
Q

CNS cells most sensitive to ischemia

A

Neurons(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1264

181
Q

Clinicopathologic syndrome arising in the setting of malignant hypertension, characterized by diffuse cerebral dysfunction, including headaches, confusion, voming, and convulsion, and sometimes leading to coma

A

Acute hypertensive encephalopathy(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1268

182
Q

Risk factor most commonly associated with deep brain parenchymal hemorrhages.

A

Hypertension(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1268

183
Q

Most common cause of bacterial meningitis in adolescents and young adults.

A

Neisseria meningitidis(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1272

184
Q

Typical CSF findings in brain abscess

A

Increased WBC, increased protein, normal glucose(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1273

185
Q

Most serious complications of chronic TB meningitis

A

Arachnoid fibrosis(producing hydrocephalus) and Obliterative endarteritis(causing arterial occlusion and infarction)(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1274

186
Q

Morphology: perivascular accumulation or lymphocytes and/or neutrophils, multiple foci of necrosis of gray and white matter, single-cell neuronal necrosis with phagocytosis of debris, microglial nodules

A

Viral Encephalitis(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1275

187
Q

It produces brain abscess, most ofen in the cerebral cortex and deep gray nuclei, central necrosis, petechial hemorrhages surrounded by acute and chronic inflammation, macrophage infiltration, and vascular proliferation; CT and MRI studies may show multiple ring enhancing lesions. SEE SLIDE 23.29.

A

Toxoplasmosis of the CNS(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1280

188
Q

A rapidly progressive encephalitis, cerebral malaria, is the complication with the highest mortality caused by what etiologic agent?

A

Plasmodium falciparum(TOPNOTCH) Robbins Basic Pathology, 9th ed., p. 1280

189
Q

HSV-1 infection has predilection to what part of the brain?

A

Temporal lobe(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1281

190
Q

This group of degenerative disorders is caused by “spreading” of misfolded proteins, allowing a pathogenic protein to acquire many of the characteristics of an infectious agent. Accumulation of PrPSC in neural tissue seems to the cause of pathologic changes in these diseases.

A

Prion diseases(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1281

191
Q

The most common prion disease that manifest clinically as a rapidly progressive dementia.

A

Creutzfeldt-Jakob Disease (TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1283

192
Q

The fundamental abnormality in this disease is the accumulation of A-beta and tau in specific brain regions.

A

Alzheimers Disease(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1288

193
Q

Syndrome caused by deletions in mitochondrial DNA, characterized by ophthalmoplegia, pigmentary degeneratation of the retina, and complete heart block

A

Kearns-Sayre syndrome(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1245

194
Q

Mitochondrial disoder caused by mutations in either mtDNA or the nuclear genome causing subacute necrotizing encephalopathy

A

Leigh syndrome(TOPNOTCH)Robbins Basic Pathology, 9th ed., p. 1245

195
Q

A 12 year old student presents with lethargy, fever, and headaches. These progress to irritability, anxiety, and confusion, with difficulty in swallowing. He refuses any drink being offered. A few days later, he slips into a coma, and dies. On history, he was bitten by a stray dog 4 months ago. At autopsy, where would the characteristic infected neurons with cytoplasmic inclusions most likely be found? (A) frontal and parietal cerebral cortex (B) hippocampus and cerebellum (C) globus pallidus and medulla (D) pineal gland and pituitary

A

hippocampus and cerebellum (TOPNOTCH) Robbins Pathologic Basis of Disease 8th ed

196
Q

A 19 year old male presents with fever and changes in mood and behavior. His neck is supple, and shows no lateralizing signs, or cranial nerve defects. Memory is impaired. A lumbar tap is performed with a slight lymphocytosis and protein elevation. Bacterial cultures were negative. On PCR, herpes simplex virus I was detected. THe histologic changes of necrotizing inflammation and Cowdry Type A bodies would most likely be found in (A) temporal lobes (B) occipital lobes (C) cerebellar vermis (D) parietal lobes

A

temporal lobes (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 876

197
Q

A 78 year old woman in a nursing home is found dead in her bed. She has had a 5 year history of progressive disorientation, memory loss, and alteration of mood and behavior. In her final year, she was mute and could not perform activities of daily living without assistance. Her relatives requested an autopsy, and her brain showed cortical atrophy with widening of the sulci. Histology showed multiple plaques and neurofibrillary tangles. The plaques are collections of neuritic processes with a central core of extracellular (A) amyloid (B) tau protein (C) glycogen (D) sphingomyelin

A

amyloid (Alzheimer disease) (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 893

198
Q

A 45 year old actor begins to experience hand tremors, and eventually develops a shuffling gait, a stooped posture, and diminished facial expressions. His mental faculties are intact. What is the expected histologic change in his brain? (A) loss of pigmented catecholaminergic neurons in his midbrain (B) loss of neurons in the striatum (C) foci of hemorrhage and necrosis in the mamillary bodies (D) multiple Lewy bodies in his cerebral cortex

A

loss of pigmented catecholaminergic neurons in his midbrain (pallor of substantia nigra in Parkinsonism) (B - Huntington disease; C - Wernicke encephalopathy; D - Lewy body dementia/disease) (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 893-894

199
Q

A 30 year old saleslady has untreated hypertension. While at work, her colleagues heard her complain of an excruciating headache then lose consciousness a few seconds later. She was pronounced dead at the ER. An autopsy is performed, which showed massive subarachnoid hemorrhage, and a ruptured aneurysm at the right anterior cerebral artery. Her kidneys were markedly enlarged, with multiple 3-4 cm diameter cysts. Which of the following is accurate? (A) the aneurysm is neoplastic (B) the aneurysm was likely present at birth (C) her kidney disease is heritable, in an autosomal dominant fashion (D) her kidney disease more commonly manifests in early childhood

A

her kidney disease is heritable, in an autosomal dominant fashion (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 569-570, 866-867

200
Q

A 26 year old backpacker presents with seizures. On imaging, there are four 1-2 cm cysts in his cerebral cortex. He undergoes surgery, where two were removed. Histopathology showed an ovoid structure with a tegument, underlying smooth muscle, three oval suckers, all surrounded by an intense inflammmatory infiltrate of plasma cells, lymphocytes, and eosinophils. The surrounding brain tissue is gliotic. The patient acquired this infection by ingesting (A) raw pork (B) raw beef (C) ova from cat litter (D) raw freshwater crabs

A

raw pork (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 880

201
Q

A 33 year old woman has been having intermittent headache for 3 years. She develops a seizure. Imaging studies show a 4 cm well circumscribed intracranial mass at the convexity of the right cerebral cortex, compressing the adjacent brain. The tumor is surgically excised, and histopathology showed cells in syncytial whorls, some in fascicles. There are occasional concentric calcifications interspersed. There is no significant mitosis, necrosis, pleomorphism, or brain invasion. Her tumor is (A) a metastasis from a thyroid primary (B) a primary lymphoma (C) a glioma (D) a meningioma

A

a meningioma (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 886

202
Q

A 40 year old lawyer presents with seizures and loss of consciousness. On imaging, there is a contrast-enhancing, intracranial mass straddling the corpus callosum, with a “butterfly” appearance. An open biopsy is performed, which showed a densely cellular tumor of with astrocytic cell processes, foci of necrosis with surrounding pseudo-palisading of tumor cell nuclei, vascular proliferation, and numerous mitoses. His tumor (A) is a glioma (B) is poorly circumscribed (C) confers a dire prognosis (D) all of the above

A

all of the above (TOPNOTCH)Robbins Basic Pathology, 8th ed., p 882

203
Q

Principal cells that are responsible for repair and scar formation in the brain (Gliosis)

A

Astrocytes. When activated, they enlarge and develop multiple stout, ramifying processes (Gemistocytic astrocyte). In long-standing gliosis, they begin to shrink, with cellular processes becoming more tighly interwoven (Fibrillary astrocyte with Rosenthal fibers) (TOPNOTCH)Robbins Basic Pathology, 9th ed., p 812

204
Q

Thick, elongated, brightly eosinophilic protein aggregates seen in astrocytic processes in CHRONIC GLIOSIS and in some LOW-GRADE GLIOMAS. SEE SLIDE 23.27.

A

Rosenthal fibers (TOPNOTCH)Robbins Basic Pathology, 9th ed., p 812

205
Q

Irreversible ischemic injury category (Early, Subacute, or Repair): Red neurons

A

Acute. 12-24 hours. (TOPNOTCH)Robbins Basic Pathology, 9th ed., p 815

206
Q

Irreversible ischemic injury category (Early, Subacute, or Repair): Necrosis, influx of macrophages, reactive gliosis

A

Subacute. 24 hours to 2 weeks. (TOPNOTCH)Robbins Basic Pathology, 9th ed., p 815

207
Q

Irreversible ischemic injury category (Early, Subacute, or Repair): Removal of necrotic tissue, gliosis (pseudolaminar necrosis)

A

Repair. More than 2 weeks. (TOPNOTCH)Robbins Basic Pathology, 9th ed., p 815

208
Q

Protein inclusion seen in Parkinson disease

A

Alpha-Synuclein. An inclusion containing alpha-synuclein is called a LEWY BODY. (TOPNOTCH)Robbins Basic Pathology, 9th ed., p 836

209
Q

Protein inclusion seen in Alzheimer disease

A

Beta amyloid and Tau protein(TOPNOTCH)Robbins Basic Pathology, 9th ed., p 836

210
Q

Alzheimer-related lesions. PLAQUE, TANGLE or TAU PROTEIN: Focal spherical collections of neuritic processes, often around a central amyloid (Beta-amyloid) core. Found in the hippocampus and amygdala usually.

A

Plaque. SEE SLIDE 23.11. (TOPNOTCH)Robbins Basic Pathology, 9th ed., p 838

211
Q

Alzheimer-related lesions. PLAQUE or TANGLE: Bundles of paired helical filaments visible as basophilic fibrillary structures. A major component is an abnormally hyperphosphorylated TAU protein. Not specific for Alzheimer’s.

A

Tangle. SEE SLIDE 23.11. (TOPNOTCH)Robbins Basic Pathology, 9th ed., p 838

212
Q

In Parkinson’s Disease, where are Lewy bodies appear first?

A

Interesingly, it appears first in the medulla, and then the pons, before involvement of the substantia nigra. (M>P>S in alphabetical order) (TOPNOTCH)Robbins Basic Pathology, 9th ed., p 839

213
Q

Often located midline in the cerebellum in children, and lateral in adults. On histology, lesion is extremely cellular with sheets of anaplastic (small blue) cells.

A

Medulloblastoma (TOPNOTCH)Robbins Basic Pathology, 9th ed., p 845

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