Micro/Path Pt 2 Flashcards
Which of the following occurs most ommonly in elferly women and is associated with postmenopausal state and estrogen deficiency?
osteogenesis imperfect
osteoporosis
myasthenia gravis
osteoarthritis
osteoporosis
FYI:
osteoarthritis is progressive erosion of articular cartilage
osteogenesis imperfetca - brittle bone, AD, poor teeth
myasthenia gravis - autoimmune, auroAB to ACh receptors at neuromuscular jct
All are features of Albers-Schonberg dz except:
anemia multiple bone fractures decreased bone density blindness deafness
decreased bone density
this is osteopetrosis
anemia is result of decreased marrow space
blindness, deafness and cranial nn involvement due to narrowing of neural foramina
multiple fractures
osteomalacia - vit D deficienct in adults
head of femur osteochondrosis
Perthes' Osgood-Schatter Kohler Scheuermann Freiberg
Perthes’ dz
tibial tuberosity osteochondrosis
Perthes' Osgood-Schatter Kohler Scheuermann Freiberg
Osgood-Schlatter
tarsal navicular bone tuberosity osteochondrosis
Perthes' Osgood-Schatter Kohler Scheuermann Freiberg
Kohler
intervertebral jts osteochondrosis
Perthes' Osgood-Schatter Kohler Scheuermann Freiberg
Scheuermann
metatarsal head osteochondrosis
Perthes' Osgood-Schatter Kohler Scheuermann Freiberg
Freiberg
Osteitis deformans present as a mized radiopaque and radiolucent lesion BECAUSE the mized stage of the dz features primnent osteolysis and osteogenesis
both true and related
osteitis deformans = Paget’s
Rickets occurs only in children; its typical adult counterpart is called:
osteitis fibrosa cystica osteitis deformans osteopetrosis osteomalacia osteomyelitis
osteomalacia
Order histologic stages of fracture healing:
A. Replacement of callus by lamellar bone
B Remodeling of bone to normal contour
C. Fracture
D. Replacement of granulation tissue by callus
E. Formation of granulation tissue around fractured bone cells
C E D A B
fat embolism often sequel of fractured bones
Most common viral cause of pericarditis:
mumps influenza herpes HIV coxsackie B and echo
coxsackie B and echo
Most common cause of right-sided heart failure:
left-sided heart failure
hypertension
ischemic heart disease
aortic and mitral valvular disease
left-sided heart failure
Causes of left heart failure:
ischemic (esp MI)
hypertension
aortic and mitral valve disease
myocardial disease
Which type of angina is characterized by prolonged or recurrent chest pain at rest?
stable angina
unstable angina
prinzmetal’s angina
variant angina
unstable
classic symptom of coronary artery disease
stable: repeated, doesn’t change in character, intensity, frequency or duration for several weeks. Predictable. Relieved by rest or vasodilators (like nitroglycerin).
unstable: variable, irregular, prolonged and recurrent at rest.
Prinzmetal’s: vasospasm, intermittent chest pain at rest.
Which is the first cardiac marker to increase after myocardial infarction?
creatine kinase
troponin
myoglobin
lactate dehydrogenase
myoglobin
MI most commonly caused by CAD.
Approximately 50% of cases of subacute (bacterial) endocarditis are caused by:
serratia
pseudomonas
staph aureus
strep viridans
strep viridans
infectious endocarditis is inflammation of heart valves
staph is most common in IV drug users
acute endocarditis - 50% is Staph
subacute - 50% is Strep viridans
fever in both
mitral valve most frequently involved
acute vs subacute endocarditis
acute is staph, subacute is strep viridans
most commonly encountered neck space infection is:
angioedema
Vincent’s angina
Ludwig’s angina
hereditary angioedema
Ludwig’s angina - extension from mandibular lower teeth into floor of mouth
Tetanospasmin is a neurotoxin that inactivates proteins that regulate the release of which of the following neurotransmitters?
glycine and 5-HT NE and epi GABA and 5-HT 5-HT and epinephrine glycine and GABA
glycine and GABA
unregulated excitatory synaptic activity, spastic paralysis, no inhibition
botulotoxin prevents release of ACh –> flaccid paralysis
Eosinophilia is often associated with
acute infx
viral infx
tuberculosis
parasitic infx
parasitic infx
also allergies
n/ph: acute bacterial infx
lymphocytes: TB, viral
monocytes: TB, malaria, ricketsia
lymphocytosis associated with
viral and TB
monocytosis assoc with
TB, malaria, ricketsia
n/ph associated with
acute bacterial infx
Link between Reye’s Syndrome and use of:
ibuprofen aspirin acetaminophen amoxicillin diphenhydramine
aspirin
Symptoms of TB include all except:
bad cough for 3 wks or longer pain in chest coughing up blood or sputum weakness or fatigue weight gain no appetite chills fever sweating at night
wt gain
primary TB: Gohn focus
secondary: activation of Ghon; favors upper lobe; tubercle formation (caseous granulomas, cavitary lesions)
secondary may be spread via lymph –> military or disseminated TB
Rebound tenderness in lower right quadrant of abdomen is characteristic of:
cholelithiasis
ulcerative colitis
hepatocellular carcinoma
acute appendicitis
acute appendicitis
Chlamydial cervicitis, the most common sexually transmitted infection, is caused byL
C. diff
c. perfringens
c. trachomatis
c. suis
c. muridarium
trachomatis
gonorrhea is caused by neisseria
Characteristic lesion of secondary syphilis is known as:
chancre
gumma
condyloma lata
condyloma acuminatum
condyloma lata
syphilis caused by treponema pallidum
primary: chancre
secondary (highly infectious): maculopapular rash and condyloma lata (flat gray) on skin and mucosal surfaces
tertiary: gumma (focal nodular mass)
condyloma acuminaum is caysed by HPV
Encephalitis is most common caused by:
bacterial infx
viral infx
fungal infx
parasitic infx
viral
An infection is pandemic if:
it has a worldwide distribution
it is constantly present at minimal levels within a population
it occurs more frequently than normal within a population
it is highly communicable
worldwide
epidemic: more frequently than normal
endemic: minimal levels
highly communicable = contagious
Acute lymphoblastic leukemia equally affects young children and adults.
This acute leukemia is most responsive to tx.
1 false, 2 true.
acute lymphoblastic - most common in children, ost responsive to tx.
acute myeloid leukemia is most malignant; 90% of adult acute leukemias.
chronic lymphocytic - least malignant, slow.
ALL vs AML vs CLL vs CML leukemias
ALL - children, responsive to tx
AML - adults, 90% of leukemias, most malignant
CLL - slow
CML - Philadelphia chromosome
Principal organ(s) involved in acute leukemia is/are the:
bone marrow
brain
lungs
kidneys
bone marrow
Philadelphia chromosome and low levels of leukocyte alkaline phosphatase are common characteristics of:
AML
ALL
CML
CLL
CML
No definitive causes have been identified for leukemia.
Possible risk factors include genetic predisposition, environmental exposure to chemicals and radiation, and viruses.
both true
viruses: HTLV, EBV
All about immunoglobulins are true except:
secreted by activated plasma cells also known as antibodies have enzymatic activity activate complement are glycoproteins
have enzymatic activity
this is false
Injection of med to someone with allergy to it leads to:
low levels of histamine
hyperglobulinemia
systemic anaphylaxis
localized anaphylaxis
systemic anaphylaxis
most common cause - allergy to penicillin
Cellular immunity is immunity mediated by: B-lymphocytes T-lymphocytes both B and T-lymphocytes neither B not T-lymphocytes
T
Of the anaphylatoxins, C3a is more stable and potent than C5a.
Only mast cells have receptors specific for C5a and C3a.
both false
C5a is more stable and potent
phagocytes, endothelial cells and mast cells have receptors for both
anaphylatoxins increase blood flow and vascular permeability
only IgG and IgM fix complement
anaphylaxis by complement components is less common than that caused by Type I (IgE-mediated) hypersensitivity
Exaggerated IgE response to environmental allergen (= atopy) manifests in all except:
dermatitis
rhinitis
jaundice
asthma
jaundice
atopic = localized Type I
atopic dermatitis = eczema
in asthma, leukotrienes
rhinitis: histamine
Which is most frequently used diagnostic technique for detection of antigens in tissue secretions or cell suspensions?
immunofluoresecence agglutination radioimmunoassay precipitation enzyme-linked immunosorbent assay
immunofluorescence
ELISA - for pt specimens, both antibodies or antigens
Which of the following major pathways of complement activation is triggered by the presence of infection, but does not involve antibody?
classical pathway
alternative pathway
lectin pathway
all of the above
alternative
lectin only specific mannose-containing PGs of bacteria
all pathways converge to C3
classical pathway of complement
Ag + AB –> C1, C4, C2 –> C3 + C5
alternative pathway of complement
infx but no AB
lectin pathway of complement
mannose in peptidoglycan
type I hypersensitivity
atopic, IgE, degranulation of mast
type II hypersensitivity
IgG-mediated cytotoxicity (–> complement or T killer)
drug allergies
type III hypersensitivity
IgG –> complement
serum sickness
type IV hypersensitivity
T-helpers (mostly Th1) sensitized, recruit destroyers
In passive immunity, antibodies are preformed in another host.
Passive immunity lasts as long as active immunity.
1 true, 2 wrong
active is slow onset but long term
Small molecule, not antigenic by itself, that can react with antibodies is called:
epitope
hapten
plasmid
immunogen
hapten
too small to eb immunogenic
epitope - specific portion of antigen to which antibody binds
Whicg of the following types of immunity os conferred by transferring lymphoid cells from actively immunized donor to a naïve or immunocompromised host?
acquired immunity humoral immunity passive immunity active immunity adoptive immunity
adoptive immunity
Complement system is a group of plasma proteins that attack pathogens.
These proteins are primatily synthesized by kidney.
First true, second wrong
mainly made by liver; C1 is made in GI epithelium
C-reactive protein - binds to bacterial in classical pathway
membrane attack complex comes after C5
Each of the following are associated with an anaphylactic hypersensitivity reaction except:
histamine heparin plt-activating factors serotonin dopamine
dopamine
IgM, IgA, and IgG are main antibodies present in blood, lymph and intercellular fluid in connective tissues.
IgA is also made in lymphoid tissues underlying mucosa and then selectively transported across mucosal epithelium to bind extracellular pathogens and their toxins on mucosal surfaces.
both true
Type II hypersensitivity rxns result from binding of antigen to antigen-specific IgE bound to its Fc receptor, principally on mast cells.
Type III hypersensitivity rxns are caused by small soluble immune complexes formed by soluble protein antigens binding to IgG made against them.
1 false, 2 true
THREE items associated with humoral immunity
provides immunity against extracellular pathogens
provides immunity against intracellular pathogens
mediated by T cells
mediated by antibodies produced by B cells
antibodies neutralize and eliminate pathogens and toxins
extracellulae
B cells
antibodies neutralize and eliminate
in contrast, cell-mediated is T against intracellular
Th activate m/ph and T-killers
All about MHC are true except:
plays a role in acute rejection of transplanted tissue
assist T-cells in recognition of intracellular pathogens
glycoprotein secreted by activated plasma cells
able to interact with T-cell receptor
coded by group of highly polymorphic genes
glycoprotein secreted by activated plasma cells
this is wrong
not secreted at all
MHCI - all cells - recognized by CD8+ - from cytosolic proteins
MHCII - only professionals (APC, m/ph, B) - CD4+ - from endocytosed proteins
Although many substances and preparations are know to be adjuvants, the only adjuvants approved for use in human vaccines are:
Freund’s complete adjuvant and Alum
Freund’s incomplete adjuvant and MF59
Immune stimulatory complexes and Alum
Alum and MF59
Alum and MF59
adjuvants allow smaller and rarer doses
Bacterial toxin that has been weakened until it is no longer toxic but is strong enough to induce formation of antibodies and immunity to the specific dz caused by the toxin is called:
antitoxin
antivenin
antiserum
toxoid
toxoid
antitoxin = antibody to toxin
Human HBIG to prevent Hep B in those not actively immunized with the Hep B vaccine is an example of
naturally acquired passive immunity
naturally acquired active immunity
artificially acquired active immunity
artificially acquired passive immunity
artificial passive
All contain attenuated virus except:
yellow fever measles rabies mumps rubella
rabies - inactivated
Each are live attenuated bacterial vaccines except
mycobacterium bovis
salmonella typhi
Yersinia pestis
coxiella burnetti
Yersinia?
has to be killed, for plague
Persons vaccinated against Hep B who have developed immunity are also immune to:
Hep A
Hep C
Hep D
Hep E
Hep D
THREE items associated with rheumatic fever
pancarditis Group B streptococci koplik spots bullous skin lesions aschoff bodies Sydenham chorea
pancarditis
aschoff bodies
Sydenham chorea
acute rheumatoid fever - group A streps!
manifestations: migratory polyarthritis, pancarditis, subcutaneous nodules, erythema, Sydenham chorea
Aschoff bodies - foci of lymphocytes in heart
All are characteristics of Addison’s excepts:
hypertension
increased pigmentation of skin
hypoglycemia
increased serum K
hypertension
characterized by hypotension
failure of adrenocortical
Osteoarthritis (degenerative joint dz) is the most common type of joint disease.
Heberden nodes, bony swellings in the distal interphalangeal joints, are a characteristic morphological changes
both true
bone polishing
dislodged pieces of cartilage in joint space
osteophytes (bony spurs) at distal (Heberden) or proximal (Bouchard) interphalangeal joints
All can be classified as type of Lagerhans cell histiocytosis except:
Letterer-Siwe
Bruton
Hand-Schuller-Christian
eosinophilic granuloma
Bruton disease
is X-linked agammaglobulinemia
Primary hyperparathyroidism is most often caused by
liver dz
parathyroid adenoma
bronchogenic squamous cell carcinoma
hypoCa of chronic renal dz
parathyroid adenoma
Systemic vasculitis in which dz
polyarteritis nodosa dermatomyositis scleroderma systemic lupus rheumatoid arthritis
polyarteritis nodosa
Skin rash in which dz
polyarteritis nodosa dermatomyositis scleroderma systemic lupus rheumatoid arthritis
dermatomyositis
Widespread connective tissue fibrosis in which dz
polyarteritis nodosa dermatomyositis scleroderma systemic lupus rheumatoid arthritis
scleroderma
butterfly rash
polyarteritis nodosa dermatomyositis scleroderma systemic lupus rheumatoid arthritis
systemic lupus
stiffness of joints which dz
polyarteritis nodosa dermatomyositis scleroderma systemic lupus rheumatoid arthritis
rheumatoid arthritis
Most common demyelinating disorder?
Devic's dz Tabes dorsalis Optic neuritis Multiple sclerosis Guillain-Barre syndrome
multiple sclerosis
female prevalence
In many cases of primary amyloidosis, the pts have some form of:
m/ph dyscrasia
erythrocyte dyscrasia
hemoglobin dyscrasia
plasma cell dyscrasia
plasma cell dyscrasia
primary amyloidosis related to abnormal production of immunoglobulins
Urticaria (hives) is a common disorder of skin characterized by localized mast cell degranulation and resultant dermal microvascular hyperpermeability. This gives rise to pruritic edematous plaques called wheals.
Angioedema is closely related to urticaria and is characterized by deeper edema of both the dermis and subcutaneous fat.
both true
Type 1 diabetes is caused by a reduction in sensitivity of insulin’s target cells.
Type 1 diabetes is more common than type 2 diabetes.
both false
1 is autoimmune, destruction of cells and absolute deficiency of insulin
2 is resistance to insulin and is more common (90-95%)
THREE items associated with rheumatoid arthritis:
joint effusions bouchard's nodes bacterial in nature fungal in nature Still-s dz osteophyte unknown cause
joint effusions
Still’s dz (RA in young ppl)
unknown cause
osteophytes - in osteoarthritis, not rheumatoid!
RA: nonsuppurative proliferative
Which is the prototype of a systemic immune complex dz?
systemic lupus erythematosus acute serum sickness poststreptococcal glomerulonephritis reactive arthritis polyarteritis nodosa
acute serum sickness
______ hypersensitivity rxns are initiated by Ag-activated (sensitized) T lymphocytes, including CD4+ and CD8+.
type I
type II
type III
type IV
type IV
which of the following antibodies are specific for systemic lupus?
anti-Sm
Anti-Jo
anti-Ro
anti-centromere
anti-Sm
particularly ANA and anti-Sm specific for SLE
acrocyanosis (Raynaud’s phenomenon) often associated with SLE