5/24 Mixed Flashcards
Wilson’s Disease
Can cause cystic degeneration of the putamen as well as damage to other basal ganglia structures.
The putamen is located medial to the insula and lateral to the globus pallidus on coronal sections.
Pseudogout
Rhomboid-shaped calcium pyrophosphate crystals
Positively birefringent under polarized light
Knee joint is involved in >50 % of cases
Hereditary Angioedema
Low serum levels of C1 esterase inhibitor
AD, episodes of painless, non-pitting, well-circumscribed edema (face, neck,lips, tongue), respiratory obstruction, abdominal pain, vomiting, diarrhea
activated kallikrein and bradykinin levels are increases
Bradykinin, C3a, and C5a mediate angioedema by increasing vasodilation and vascular permeability
SE of ACEi = angioedema (bradykinin accumulation)–ACEi are CONTRAINDICATED in patients with hereditary angioedema
Teratogenic Medications: Phenytoin
Neural tube defects, orofacial clefts, microcephaly, nail or digit hyperplasia
Teratogenic Medications: Lithium
Ebstein anomaly, nephrogenic diabetes insipidus, hypothyroidism
Teratogenic Medications: Valproate
Neural tube defects
Teratogenic Medications: Isotertinoin
Microcephaly, thymic hypoplasia, small ears, hydrocephalus
Teratogenic Medications: Methotrexate
Limb and craniofacial abnormalities, neural tube defects, abortion
Teratogenic Medications: ACE inhibitors
Renal dysgenesis, oligohydramnios
Teratogenic Medications: Warfarin
Nasal hypoplasia, stippled epiphysis
MOA of penicillins and cephalosporins
Irreversibly bind to penicillin-binding proteins such as TRANSPEPTIDASES
Long term treatment of Parkinson disease with levodopa
Complicated by periodic and sometimes unpredictable fluctuations in motor function
This “on-off” phenomenon is thought to be a consequence of progressive nigrostriatal neurodegeneration leading to a decreased therapeutic window for levodopa
SE Dihydropyridine Ca Channel Blockers (Amlodipine)
Headache, Flushing, Dizziness, Peripheral Edema
Pituitary Apoplexy
Acute hemorrhage into the pituitary gland
Associated with preexisting pituitary adema
Presents acutely with severe headache, cranial nerve involvement (bitemporal hemianopsia, opthalmoplegia), and signs of meningeal irritation
Pts often have chronic symptoms associated with the underlying pituitary tumor
Cardiovascular collapse can occur due to adrencortical deficiency
Acute pancreatitis
80% due to gallstones and chronic alcoholism
Less common causes account for the other 20%
Inherited or acquired hypertriglyceridemia (>1000) can cause acute pancreatitis
Cryptorchidism
The seminiferous tubules become atrophic and hyalinized as a result of temperature induced damage, resulting in significantly depressed sperm count as well as decreased inhibin levels
Hormonal function of leydig cells is usually not impaired , thus secondary sexual characterisitcs and sexual performance are normal
Should be corrected early in life to prevent damage to ST and decrease risk of testicular cancer
Enveloped viruses
Acquire their lipid bilayer envelope by budding through the plasma membrane of the host cell
Exceptions include the herpesviruses, which bud through the acquire their envelope from the host cell nuclear membrane
Wernicke Encephalopathy
Pyruvate dehydrogenase and a-ketoglutarate dehydrogenase require thiamine as a cofactor
Administration of glucose to thiamine-deficient patients (alcoholics) can result in Wernicke encephalopathy (acute confusion, opthalmoplegia, ataxia) due to increased thiamine demand
Multiple sclerosis incontinence
Often develop a spastic bladder a few weeks after developing an acute lesion of the spinal cord
These patients present clinically with increased urinary frequency and urge incontinence
Urodynamic studies show the presence of bladder hypertonia
Cleavage of proinsulin
Occurs in the islet cell secretory granules
Yields insulin and C-peptide
Both are stored in the granule until they are secreted in equimolar amounts
Phenotype mixing
Refers to coinfection of a host cell by 2 viral strains, resulting in progeny virions that contain nucleocapsid proteins from one strain and the unchanged parental genome of the other strain
Because there is no change in the underlying viral genomes (no genetic exchange), the next generation of virions revert to their original, unmixed phenotypes