Содержание

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Memory loss Dementia Cognitive impairment or memory loss Onset: insidious Duration:

Memory loss

Dementia

Cognitive impairment or memory loss
Onset: insidious
Duration: irreversible
Chronic
Permanent

Amnesia

Memory loss

Delirium

Cognitive impairment or

memory loss
Onset: rapid
Duration: reversible
Waxes and wanes over time
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Alzheimer’s disease

Alzheimer’s disease

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Alzheimer’s disease

Alzheimer’s disease

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Alzheimer’s disease

Alzheimer’s disease

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Alzheimer’s disease Sporadic and Familial (PSEN-1 or PSEN-2 mutation and trisomy

Alzheimer’s disease

Sporadic and Familial (PSEN-1 or PSEN-2 mutation and trisomy 21)
Symptoms:

short-term memory loss-> loss of motor skills and language-> long-term memory loss-> more disoriented-> bedridden->death

Diagnosis: clinical, brain biopsy,
CT (cortical atrophy)
Treatment: no cure, supportive care, family education.
Cholinesterase inhibitors: Tacrine, Donepezil, Rivastigmine, Galantamine

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Pick’s disease

Pick’s disease

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Pick’s disease Frontotemporal degeneration Behavior and personality change goes first (remain

Pick’s disease Frontotemporal degeneration

Behavior and personality change goes first (remain memory)
Then dementia,

aphasia, parkinsonian aspects
Diagnosis: Clinical, CT-frontotemporal degeneration
Treatment: supportive
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Lewy-body dementia

Lewy-body dementia

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Lewy-Body dementia Early symptoms: difficulty focusing, poor memory, visual hallucination, disorganized

Lewy-Body dementia

Early symptoms: difficulty focusing, poor memory, visual hallucination, disorganized speech

and depression
Later symptoms: resting tremor, stiff and slow movements, reduced facial expression
Sleep disorders
Diagnosis: clinical, biopsy
Treatment: cognitive sym. – donepezil, motor sym. - levodopa
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Vascular dementia

Vascular dementia

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Vascular dementia Multi-infarct dementia Symptoms: Very depend on which region of

Vascular dementia Multi-infarct dementia

Symptoms:
Very depend on which region of the brain

is damage
Stepwise decline
Diagnosis: Clinical, neuropsychological test, CT or MRI
Treatment: reducing rick of repeated strokes
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CJD

CJD

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CJD Caused by prions From sporadic mutation, abnormal gene, uncooked meat

CJD

Caused by prions
From sporadic mutation, abnormal gene, uncooked meat
30-40s ages
Symptoms: sleep

disorders, visual deterioration, loss of coordination, cognitive impairment, personality change
Diagnosis: clinical
Treatment: supportive
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Normal Pressure Hydrocephalus

Normal Pressure Hydrocephalus

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Normal Pressure Hydrocephalus Due to increased ICP Symptoms: urinary incontinence, ataxia,

Normal Pressure Hydrocephalus

Due to increased ICP
Symptoms: urinary incontinence, ataxia, dementia
Diagnosis: CT

– hydrocephalus
LP – get improvement of condition
Treatment: VP shunt
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Huntington’s disease

Huntington’s disease

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Huntington’s disease Inherited disorder Uncontrolled movement – chorea, unsteadiness, clumsiness, loss

Huntington’s disease

Inherited disorder
Uncontrolled movement – chorea, unsteadiness, clumsiness, loss of balance,

slurred speech, trouble swallowing and eating
Diagnosis: clinical (chorea + abnormal behavior + dementia + family)
Treatment: supportive
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Intracranial tumors

Intracranial tumors

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Brain cancer Primary 30%(singular) and secondary 70%(multiple lesions) Symptoms: focal neurologic

Brain cancer

Primary 30%(singular) and secondary 70%(multiple lesions)
Symptoms: focal neurologic deficit, seizure,

headache worse in the morning
Diagnosis: MRI with contrast, CT, biopsy
Treatment: resection, radiation or/and chemo, steroids, seizure profilaxis
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Glioblastoma Multiforme Adults Highly malignant tumor Product of parenchyma and tends

Glioblastoma Multiforme

Adults
Highly malignant tumor
Product of parenchyma and tends to cross

the corpus callosum
Ring-enhancing lesion or Bat’s wing deformation
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Oligodendroglioma Adult forms from oligodendrocytes can occur in the brain or

Oligodendroglioma

Adult
forms from oligodendrocytes
can occur in the brain or spinal cord
Histology:

chicken wire capillary pattern, ”fried egg” cell, calcified tumor
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Meningioma Adult Benign, superficially located Product of Dura Histology: psammoma bodies,

Meningioma

Adult
Benign, superficially located
Product of Dura
Histology: psammoma bodies, spindle cells
Treatment: resection and

curative
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Hemangioblastoma Adult Blood vessel origin EPO producing Histology- thin walled capillaries

Hemangioblastoma

Adult
Blood vessel origin
EPO producing
Histology- thin walled capillaries

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Pituitary gland

Pituitary gland

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Pituitary Adenoma Prolactinoma Premenopausal females: Hypogonadism, oligomenorrhea or amenorrhea, galactorrhea Males:

Pituitary Adenoma

Prolactinoma

Premenopausal females: Hypogonadism, oligomenorrhea or amenorrhea, galactorrhea
Males:
Decrease libido, impotence,

infertility
Dx: prolactin, MRI
Tx: Cabergoline

Acromegaly

Kids: gigantism
Adults: acromegaly hands, feet, face and visceral organs, diabetes and diastolic heart failure
Dx: IGF1 glucose suppression test
Tx: surgery, Octreotide, Debulking or radiotherapy

Cushing disease

Mood face, buffalo hump, truncal obesity
Dx: ACTH
Tx: surgery, radiation therapy, Metyrapone

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Acromegaly

Acromegaly

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Non- functional pituitary adenoma Usually macroadenomas Compression symptoms: headache &visual impairment

Non- functional pituitary adenoma

Usually macroadenomas
Compression symptoms: headache &visual impairment
Bitemporal hemianopia
Double vision
Diagnosis:

MRI, visual field testing
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Schwannoma Adult Occur at the cerebellopontine angle Damage of CN7 & CN8 Histology: S-100+

Schwannoma

Adult
Occur at the cerebellopontine angle
Damage of CN7 & CN8
Histology: S-100+

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Childhood tumors Infratentorial tumors Pilocytic Astrocytoma From Astrocytes Rosenthal Fibers Medulloblastoma

Childhood tumors

Infratentorial tumors

Pilocytic Astrocytoma
From Astrocytes
Rosenthal Fibers
Medulloblastoma
From embryonic stem cells and primitive

neuroendocrine cells
Homer-Wright rosettes
Ependymoma
From neuroglial cells
Perivascular pseudorosettes

Supratentorial tumors

Craniopharyngioma
From remnants of Rathke’s pouch
Above the sella turcica compress the pituitary gland
Pinealoma
From pinocytes or germ cells
Parinaud syndrome
Paralysis of upward gaze
Pupillary light-near dissociation
Convergent-retraction nystagmus