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13 Cards in this Set

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Syphilis
Treponema pallidum
- Spirochetes
- Treponemes - 6-15u
- Corkscrew shaped, motile
- Outer mb similar to gram negative bacteria
- Very fragile cells
-CANNOT grow in vitro
Other pathogenic treponemes cause significant morbidity worldwide.
- Primarily skin and mucous mb infections, not sexually transmitted
T. pallidum
Transmitted by direct contact only
- Enters the body via skin and mucous mb through abrasions during sexual contact
- Transmitted transplacentally to fetus during pregnancy
Disease professes in stages
- Travels via the lymphatic system to regional lymph nodes then throughout the body via the blood stream
- Invasion of the CNA can occur during any stage of infection
May become chronic without treatment
3 stages of disease if untreated: Primary stage
PRIMARY
- Incubation period 10-90 days
- Development of characteristic primary lesions "hard chancre" ---- At site of infection, painless, resolves spontaneously in 4-6 wks
- Regional lymphadenopathy
- Serologic tests may no be positive during early primary syphilis
Secondary stage
- 2-8 wks after appearance of chancre, may persist for weeks or months
- May overlap with primary stage
- Mucocutaneous lesions most common
- Manifestations: Flulike symptoms, rash (75-100%), lymphadenopathy, mucous patches, alopecia
- May or may not have CNS involvement
- Serologic tests usually have highest titer during this stage
Latent syphilis and neurosyphilis
Latent syphilis
- Host suppresses infection - no lesions
- Positive serology
Neurosyphilis
- Organisms invade the CNS
- May occur at any stage of infection
- Can be asymptomatic
- Manifestations: acute syphilitic meningitis, ocular involvement
Tertiary stage and congenital syphilis
- AProx 30% of untreated patients progress to this stage 3-50 years after infection
- Rarely seen today because of availability of Antibiotis
- Gumas: destructive granulomatous leions
- Possible cardiac symptoms
- Possible CNS involement
- Usually fatal
Congenital syphilis
- Transplacental transmission, can occur during any trimester
- Risk of transmission higher in primary and secondary stages of disease
- May result in developmental disorders, deafness, and bone deformities
Dx
- Clinical history, physical exam, and laboratory dx
- Identification of microorganisms in lesions by
DARKFIELD microscopy
DIRECT fluorescent Ab - T. pallidum (DFA -TP)
- Serological testing for treponemal (Ag- specific) and non-treponemal Abs
NON-TREPONEMAL: VDRL ,RPR
TREPONEMAL: FTA - Abs and microhemagglutination T.pallidium (MHA-TP)
Direct observation: Darkfield microsopy
- T.pallidum morphology and mobility
Advantage: Definitive immediate dx
Disadvantage: REQUIRES specialized equipment and experienced microscopist, POSSIBLE confusion with other pathogenic and non-pathogenic spirochetes, NOT recommended for oral lesions, POSSIBILITY of false negative
Direct observation: DFA -TP
Ids organism in direct lesion smear by immunoflourescence
Advantages: COMMERCIALLY available reagents, COMPARES favorably with dark field microscopy
Disadvantages: LONGER turn around time
Non- Treponemal Tests
- Can be qualitative and quantitative
- Positive non-treponemal tests should be followed up with confirmation using treponemal specific tests
- Principle: measure Ab against cariolipin-lecitin-cholesterol Ag
- Not specific for T. pal
- Titers usually correlate with disease activity and results are reported quantitatively
- RPR and VDRL - flocculation tests
- RPR - most widely used on unheated serum: charcoal added allows for macroscopic reading
- VDRL - can be used on CSF for Dx of neurosyphilis: read microscopically
Non-Treponemal test (Adv vs. Disadv)
Adv:
- Rapid and inexpensive
- Easy to perform and can be done in clinic or office
- Quantitative
- Used to follow response to therapy
- Can be used to evaluate possible reinfection
Disadv:
- May be insensitive in certain stages
- False positive rxn do occur
- Przone effect may cause false negative (rare)
Treponemal methods
- Measure Ab directed against T. pal Ag
- Tests are qualitative
- Usually reactive for life
- Used to confirm "pos" on non- treponemal tests
FTA - ABS : killed suspension of organisms fixed to slide
MHA- TP : microhemagglutination --- Agglutination by specific Abs in pts serum with sheep RBCs sensitized to T. pal Ag
Sensitivity of serological assays
- Detection by serology related to both stage of disease and test method
- 90% of pts positive after 3 weeks
- Secondary stage pts are serologically positive
- Late syphilis- treponemal tests- positive
NON- treponemal tests are non-reactive