Shit list 2 - Neuro Flashcards
Pilocytic Astrocytoma
Kids MCC.
Benign.
Posterior fossa i.e. cerebellum, but can be supratentorial.
GFAP +.
Rosenthal fibres (eosinophilic, corkscrew), spindle cells.
Cystic and solid.
Medulloblastoma
Kids, 2nd MCC.
Highly malignant.
Type of PNET.
Compress 4th ventricle –> hydrocephalus and drop mets.
Always cerebellum, MC = vermis.
Homer-Wright rosettes.
Solid, small blue cells, high mitotic index.
Ependymoma
Kids.
4th ventricle ependymal cells, so can cause hydrcephalus.
[adults MC is spine].
Perivascular pseudo-rosettes.
Rod-shaped blepharoplasts (basal ciliary bodies) near nucleus
Craniopharyngeoma
Kids.
Benign.
Supra-tentorial.
Confused with pituitary adenoma as both cause bitemporal hemianopsia.
From rathke’s pouch derivatives, so can calcify.
Pleiomorphic xanthoastrocytoma
Kids/teens.
Sudden onset seizures.
Leptomeningeal, reticulin deposits, chronic inflammatory cells.
CYP 450 Inducers
Chronic alcoholism. St. John's Wort. Phenytoin. Phenobarbital. Carbamazapine. Nevirapine (NNRTI). Rifampin. Greisofulvin. Benzopyrines.
CYP450 Inhibitors
Acute alcohol abuse. Ritonavir (protease). Amiodarone (III). Cimetidine. Ketoconazole. Isoniazid (INH). Grapefruit juice. Quinidine (Ia). Macrolides (not A, esp E) Omeprazole Ciprofloxacin
Common CYP 450 substrates
Warfarin.
Anti-epileptics.
Theophylline.
OCP.
Lithium: use, AE, toxicities
Use: bipolar and SIADH
AE: tremor, nephrogenic DI, hypothyroidism, Ebstein anomalie
Toxicity: via thiazides
Atypical Antipsychotics: names, use, general AE. specific AE
Names: Quetiapine, olanzapine, risperidone, aripooprazole, ziprasidone, clozapine
Use: schizophrenia, bipolar, OCD, anxiety disorders, depression, mania, tourette’s
AE: QT prolongation
Spec AE:
- O/C = weight gain
- C = agranulocytosis (weekly WBC) and seizures (and weight gain)
- R = prolactin
DOC trigeminal neuralgia
Carbamazapine
Myotonic dystrophy: inheritance, s/s
AD.
CTG repeat.
Type I fibre destruction.
S/S: myotonia (can’t release door knobs), muscle wasting, frontal baldness, arrhythmia, testicular atrophy, cataracts
Glioblastoma Multiforme
Adult.
MC malignant (1yr).
Can cross corpus callous to other hemisphere.
GFAP +.
Pseudopallisading, pleiomorphic, central necrosis and hemorrhage
Meningioma
Adult. Benign. Convexities and parasaggital; extra-axial and may have tail. From arachnoid cells. Seizures of focal neurological signs. Whorrled spindle-cells, psammoma bodies.
Hemangioblastoma
Adult. Cerebellar. VHL when also have retinal. Thin-walled capillaries. Can make EPO.
Schwannoma
Adult. @ cerebello-pontine angle MC. S-100+. common on VIII - tinnitus, vertigo, sensory hearing loss - CONSTANT (ddx = mennieres = episodic). Bilateral VII = NF-2
Oligodendroglioma
Adult. Frontal lobe white matter. Chicken wire capillaries. Fried eggs Often calcify
uveitis: causes
Systemic inflammatory diseases: B-27, sarcoidosis, RA, juvenile idiopathic arthritis
Retinal detachment
Separation of photo-R layer from RPE –> photoreceptors degenerate –> vision loss.
Secondary to retinal breaks, diabetic traction, inflammatory effusions.
splaying and paucity of retinal vessels.
Flashed and floaters, then curtain drawn down on vision. Emergency
Central retinal artery occlusion
Acute. Painless monocular vision loss. Cloudy/pale retina. Attenuated vessels. *Cherry red fovea* MCC is ICA embolism --> opthalamic a. --> retinal a.
Retinitis pigmentosa
Inherited retinal degeneration.
Starts with night blindness.
Bony spicule shaped deposits.
Retinitis
Retinal edema and necrosis.
Via infection - HSV, VZV, CMV.
Also associated with immunosuppression.
pupillary light reflex
4 neurons. CN II (n1) --> pretectal nucleus (midbrain) --> bilateral n2 -->EW nucleus --> n3 --> ciliary ganglion --> short ciliary (n4) --> pupillary spincter muscles
N4 cell body degeneration = Adie’s pupil (mono argyll-robertsons)