UWorld Incorrects Flashcards
(389 cards)
What is the antidote for severe Serotonin Syndrome?
Cyproheptadine: 1st gen Antihistamine with nonselective serotonin antagonist (5-HT1 and 5-HT2)
How can you inhibit a shorter growth spurt in a child who is female who has Idiopathic precocious puberty?
Inhibit estrogen effects on long bone epiphyseal plate.
Describe Strep Agalactiae (GBS)
5 points
- Catalase negative
- beta hemolytic
- PYR negative (Pyrrolidony Arylamidase)
- CAMP positive (Christie, Atkins and Much- Petersen test)
- Causes neonatal sepsis, meningitis, UTI
Describe the E Coli virulence factor: P. Fimbriae
- allows adhesions to urothelium
- Presents as UTI
Gram negative bacilli, cannot ferment lactose, is not oxidase-positive, and can produce H2S:
Proteus and Salmenella
Gram negative bacilli, slow lactose fermenter:
Citrobacter and Serratia
Describe Strep Viridans
- Catalase negative
- Alpha- hemolytic (partial green hemolysis)
- Optochin-resistant
- Bile insoluble
- Found in dental carries
- Responsible for subacute endocarditis
Describe Strep Pneumoniae
- catalase negative
- optochin- sensitive
- bile soluble
- alpha hemolytic (partial green hemolysis)
- causes meningitis, otitis media, Pneumonia, Sinusitis
Describe Strep Pyogenes (GAS)
- catalase negative
- beta hemolytic
- PYR positive (Pyrrolidonyl Arylamidase)
- Bacitracin Sensitive
- Causes Scarlet fever, Rheumatic fever, and PSGN
Describe Enterococcus
- Catalase negative
- Gamma hemolytic
- Growth in Bile and 6.5% NaCl
- causes UTI, Cholecystitis, and subacute endocarditis
Describe Strep Gallolyticus
5 points
- catalase negative
- gamma hemolytic
- growth in bile, not in NaCl
- PYR-Negative
- responsible for Bacteremia associated with colorectal cancer
Describe the features of MHC II:
Structure: Alpha and Beta polypeptide chains
Location: APC’s (B-cells, macrophages, dendritic cells, langherans cells)
Type of Ag: Bacterial from lysosomes.
Antigen Presentation: Activates TH cells, when stimulated results in the humoral and cell-mediated immune response.
Describe the erythematous childhood rash: German Measles (Rubella)
- Caused by Rubella Virus ( Enveloped, ssRNA positive sense, Togaviridae family, Rubivirus genus)
- Clinical presentation: Maculopapular rash starting on head, progressing to trunk and extremities, also occipital and post-auricular lymphadenopathy.
- Complication: Congenital Rubella Syndrome
Dermatology Pathology:
Describe the Erythamatous rash in childhood: Roseola Infantum
- Caused by HHV 6 (Enveloped dsDNA, Icosahedral shape, Herpesviridae family)
- High fever for 3-5 days with rash after fever subsides. Macules and papule initially at truck that spreads to extremeties.
- Complications are self limited.
Describe Actinomyces Israelli
- gram positive bacterium that grows in filaments.
- causes a cervicofacial infection that slowly evolves into multiple abscesses and draining sinus tracts with yellow “sulfur” granules.
- Histopath: chronic inflammatory granulation tissue surrounding dense fibrosis.
Describe Statin Myopathy:
Myocyte Necrosis caused by increase concentration of Statin drugs, mostly due to Cyp450 inhibition. Severe cases rhabdomyolysis and AKI (elevated BUN and creatinine), dark urine.
Cyp450 inhibitors: Cyp3A4
- Non-dihydropyridine CCBs: Verapamil, diltiazem.
- Macrolides: Erythromycin, Clarithromycin.
- Protease Inhibitors: Ritonavir, Soquinavir)
- OATP inhibitors: Cyclosporine
- Corticosteroids, Fibrates, Colchicine, Ketoconazole
Statin of choice to prevent this is Pravastatin.
Describe Lichen Planus
Clinical findings:
- 5 ‘p’s’: pruritic, purple/pink, polygonal, papule, plaques
- Lacy, white network (Wickman Striae)
- Locations: Skin (e.g. wrist, ankles), oral mucosa/white papule and plaques and erythema, (mucosal cetrophy ulcers), Geritalia
*Path. findings: Hyperkeratosis, Lymphocytic interface dermatitis, Eosinophilic colloid (civatte) bodies, thickened stratum granulosum, sawtooth ridges Rete
*Hx: Chronic symptoms. Form. of Lesions at sites of trauma (Köbner phenom.) Resolve 2 yr. Mucosal recur./persist.
Describe the pathway of CSF
- Lateral Ventricles
- Interventricular foramina of Monro
- 3rd Ventricle
- Cerebral aqueduct of Sylvius
- 4th Ventricle
- Lateral foramina of Lusaka or midline of Magendie
- Subarachnoid space
Describe Syringomyelia:
- Formation of a cavity (syrinx) in the cervical region of the spinal cord.
- The syrinx damages the ventral white commissure, leading to BL loss of pain and temperature of the affected levels (typical arms and hands), distal sensation is preserved.
- Destruction of ventral horns results in flaccid paralysis and atrophy of the intrinsic muscles of the hand.
Describe Aplastic Anemia:
-Pathogenesis: Multipotent hematopoietic stem cells destroyed by cytotoxic T cells or direct cytotoxic injury –> bone marrow aplasia/hypoplasia –> lack of circulating peripheral blood cells.
*Common triggers: Autoimmune, drugs: cytotoxic chemotherapy, immunosuppresants, idiosyncratic reactions. Ionizing radiation and toxins. Viral infections (eg. viral hepatitis, HIV)
*Manifestations: anemia, thrombocytopenia, leukopenia.
Describe pure red cell aplasia:
Rare form of bone failure characterized by severe anemia with reticulocytopenia and morphologically normal platelets and leukocytes. Most common with Thymoma, Lymphocytic leukemia, and parvovirus B19 infection.
Describe IgA Vasculitis (Henoch-Schönlein purpura):
*Pathogenesis: Deposition of IgA immune complex in small vessels
- activates compliment.
- Neutrophillic inflame and vascular damage.
- often follows a URI
*Clinical Manifestations:
- Palpable purpura/petichiae on the lower extremities and
buttocks.
- Arthritis/arthralgia, abdominal pain, GI bleed intersusception,
renal disease (hematuria w/ w/o protein)
*Dx: Usually clinical
- Skin Bx: Leukoclastic vasculitis, IgA deposition in vessel walls
List the anomalies associated with Trisomy 21:
- Neuro: Intellectual disability, Early onset Alzheimer Disease
- Cardiac: Complete AV Septal Defect, VSD, ASD
- GI: Duodenal Atresia, Hirschsprung Disease
- Endo: Hypothyroidism, T1DM, Obesity, Short Stature
- Oncologic: Acute Leukemia (ALL)
- Orthopedic: Atlantoaxial instability
Describe Hereditary Angioedema:
- Recurrent episodes of cutaneous or mucosal swelling due to C1
inhibitor deficiency. - C4 levels are low due to inhibited cleavage of C4 by excess activated
C1 - Elevated bradykinin causes vasodilation and increase vascular
permeability resulting in edema.