Treponema pallidum pallidum: Difference between revisions
From IDWiki
Treponema pallidum pallidum
No edit summary |
(→: added CSF, and also capitalized titles) |
||
Line 1: | Line 1: | ||
==Background== |
==Background== |
||
* |
*Causes '''syphilis''' |
||
===Microbiology=== |
===Microbiology=== |
||
Line 27: | Line 27: | ||
**Late (≥ 2 years) |
**Late (≥ 2 years) |
||
===Primary |
===Primary Syphilis=== |
||
*Incubation period is about 3 weeks |
*Incubation period is about 3 weeks |
||
Line 40: | Line 40: | ||
*Serology often negative in early syphilis |
*Serology often negative in early syphilis |
||
===Secondary |
===Secondary Syphilis=== |
||
*Incubation period 3 weeks to 3 months |
*Incubation period 3 weeks to 3 months |
||
Line 54: | Line 54: | ||
*Less common: condyloma lata, aseptic meningitis, iritis, mucosal white patches, glomerulonephritis, paroxysmal nocturnal hemoglobinuria, hepatitis |
*Less common: condyloma lata, aseptic meningitis, iritis, mucosal white patches, glomerulonephritis, paroxysmal nocturnal hemoglobinuria, hepatitis |
||
===Latent |
===Latent Syphilis=== |
||
*High rate of relapse of secondary syphilis within the first 1-2 years following infection (but especially within the first year) |
*High rate of relapse of secondary syphilis within the first 1-2 years following infection (but especially within the first year) |
||
===Tertiary |
===Tertiary Syphilis=== |
||
*Eventually occurs in about 30% of untreated cases |
*Eventually occurs in about 30% of untreated cases |
||
Line 84: | Line 84: | ||
*Later, coarse tremors, Argyll-Robinson pupil, paresis |
*Later, coarse tremors, Argyll-Robinson pupil, paresis |
||
=====Tabes |
=====Tabes Dorsalis===== |
||
*Occurs in 2-9% of cases of untreated syphilis |
*Occurs in 2-9% of cases of untreated syphilis |
||
Line 99: | Line 99: | ||
*Others |
*Others |
||
====Cardiovascular |
====Cardiovascular Syphilis==== |
||
*Occurs in 10% of people with untreated syphilis |
*Occurs in 10% of people with untreated syphilis |
||
Line 107: | Line 107: | ||
*Diagnosed by RPR +/- CMIA |
*Diagnosed by RPR +/- CMIA |
||
====Gummatous |
====Gummatous Syphilis==== |
||
*Gummas are necrotizing granulomatous lesions |
*Gummas are necrotizing granulomatous lesions |
||
Line 115: | Line 115: | ||
*CNS lesions look like toxo, so beware in HIV patients |
*CNS lesions look like toxo, so beware in HIV patients |
||
===Other |
===Other Presentations=== |
||
*Isolated auditory syphilis |
*Isolated auditory syphilis |
||
Line 125: | Line 125: | ||
*In Ontario, we do a treponemal test to screen (CMIA), then repeat it with a more specific treponemal test (TPPA) alongside RPR |
*In Ontario, we do a treponemal test to screen (CMIA), then repeat it with a more specific treponemal test (TPPA) alongside RPR |
||
===Direct |
===Direct Visualization=== |
||
*Darkfield microscopy |
*Darkfield microscopy |
||
Line 134: | Line 134: | ||
**Best to use in primary syphilis |
**Best to use in primary syphilis |
||
===Non- |
===Non-Treponemal Tests (VDRL/RPR)=== |
||
*Veneral Diseases Research Laboratory (VDRL) has been replaced by the [[rapid plasma reagin]] (RPR) test |
*Veneral Diseases Research Laboratory (VDRL) has been replaced by the [[rapid plasma reagin]] (RPR) test |
||
Line 144: | Line 144: | ||
*Tests will eventually become nonreactive |
*Tests will eventually become nonreactive |
||
===Treponemal |
===Treponemal Tests=== |
||
*More specific and sensitive, but more expensive |
*More specific and sensitive, but more expensive |
||
Line 156: | Line 156: | ||
**'''''T. pallidum'' enzyme immunassay (TP-EIA)''' |
**'''''T. pallidum'' enzyme immunassay (TP-EIA)''' |
||
===Interpretation of |
===Interpretation of Serology=== |
||
{| class="wikitable sortable" |
{| class="wikitable sortable" |
||
!CMIA screen |
!CMIA screen |
||
Line 199: | Line 199: | ||
|} |
|} |
||
=== Lumbar Puncture for CSF === |
|||
==Treatment== |
|||
⚫ | |||
* Should be done routinely when: |
|||
** Neurological (including optic and auditory) signs or symptoms |
|||
** Failure of serologic response |
|||
** Tertiary syphilis |
|||
** Congenital syphilis |
|||
** In patients with HIV: |
|||
*** CD4 ≤350 |
|||
*** RPR ≥1:32 |
|||
* The sample should be sent for cell count and differential, protein, and either VDRL (not RPR) or FTA-Abs |
|||
==Management== |
|||
⚫ | |||
*[[Is treated by::Benzathine penicillin G]] 2.4 million units IM once, divided between two buttocks |
*[[Is treated by::Benzathine penicillin G]] 2.4 million units IM once, divided between two buttocks |
||
Line 206: | Line 218: | ||
*Alternative (penicillin allergy and pregnancy): penicillin desensitization or [[Is treated by::azithromycin]] |
*Alternative (penicillin allergy and pregnancy): penicillin desensitization or [[Is treated by::azithromycin]] |
||
===Late |
===Late Latent and Tertiary (excluding neurosyphilis)=== |
||
*[[Is treated by::Benzathine penicillin G]] 2.4 million units IM q1week for 3 weeks |
*[[Is treated by::Benzathine penicillin G]] 2.4 million units IM q1week for 3 weeks |
||
Line 212: | Line 224: | ||
*Monitor response with RPR titres, which should drop 4-fold within 6 months |
*Monitor response with RPR titres, which should drop 4-fold within 6 months |
||
===Tertiary |
===Tertiary Neurosyphilis=== |
||
*[[Is treated by::Penicillin G]] 4 million units IV q4h for 10 to 14 days |
*[[Is treated by::Penicillin G]] 4 million units IV q4h for 10 to 14 days |
||
*Often followed by at least one dose of IM benzathine penicillin, sometimes weekly for 2-3 weeks |
*Often followed by at least one dose of IM benzathine penicillin, sometimes weekly for 2-3 weeks |
||
===Congenital |
===Congenital Syphilis=== |
||
*If <1 month of age: [[Is treated by::crystalline penicillin G]] 50 kU/kg IV q12h for the first week of life and q8h thereafter, for a total of 10 days |
*If <1 month of age: [[Is treated by::crystalline penicillin G]] 50 kU/kg IV q12h for the first week of life and q8h thereafter, for a total of 10 days |
Revision as of 15:01, 15 August 2020
Background
- Causes syphilis
Microbiology
- Small, slow-growing spirochete
- Not seen on standard microscopy; requires darkfield microscopy
Clinical Presentation
Stages
- Primary syphilis (incubation period 3 weeks [range 3 to 90 days])
- Secondary syphilis (incubation period 2 weeks to 3 months [range 2 weeks to 6 months])
- Latent
- Early latent (<1 year)
- Late latent (≥1 year)
- Tertiary syphilis (incubation period years to decades)
- Cardiovascular (incubation period 10 to 30 years)
- Gummatous (incubation period 15 years [range 1 to 46 years])
- Neurosyphilis (incubation period 2 to 20 years)
- Meningovascular
- Parenchymatous
- Tabes dorsalis
- Congenital
- Early (< 2 years)
- Late (≥ 2 years)
Primary Syphilis
- Incubation period is about 3 weeks
- Chancre
- Ulcerative lesion
- Clean borders
- Indurated
- Not painful unless secondarily infected
- Lasts 2 to 6 weeks
- May present with regional lymphadenopathy
- Diagnosis with darkfield microscopy, fluorescent antibody smear, or (most commonly) serology
- Serology often negative in early syphilis
Secondary Syphilis
- Incubation period 3 weeks to 3 months
- Often no history of chancre
- Diffuse maculopapular rash that involves palms and soles
- Typically begins on trunk
- Start as pinkish-reddish macular lesions that evolve into brownish-reddish papules that may have scaling
- May progress to pustular lesions (pustular syphilids)
- May be itchy
- Can be isolated to palms and soles
- Generalized lymphadenopathy
- Fever, chills, arthralgias
- Less common: condyloma lata, aseptic meningitis, iritis, mucosal white patches, glomerulonephritis, paroxysmal nocturnal hemoglobinuria, hepatitis
Latent Syphilis
- High rate of relapse of secondary syphilis within the first 1-2 years following infection (but especially within the first year)
Tertiary Syphilis
- Eventually occurs in about 30% of untreated cases
Neurosyphilis
- Of the 25-60% of people who have CNS invasion, 95% are asymptomatic during the early stage and 80% of those spontaneously clear it
- Incubation period is 7-15 years
- Three major presentations: meningovascular syphilis, parenchymous syphilis, and tabse dorsalis
Meningovascular
- Possibly the most common neurosyphilis
- Subdivided into cerebromeningeal (diffuse or focal) and cerebrovascular
- Stroke-like symptoms, especially MCA or basilar territory
- Can present as a sudden change, as syphilitic apoplexy
- Can present following a prodrome of weeks to months of non-specific headaches, vertigo, irritability, insomnia, and personality changes
Parenchymatous
- Previously known as "generalized paresis of the insane"
- Occurs in 2-5% of cases of untreated syphilis
- Commonly found on psychiatric wards
- Causes psychosis and dementia
- Later, coarse tremors, Argyll-Robinson pupil, paresis
Tabes Dorsalis
- Occurs in 2-9% of cases of untreated syphilis
- Isolated posterior cord degeneration leading to a loss of proprioception in the lower extremities
- Stomp the ground when walking to use intact pain/pressure sensation
- Loss of sensation in the Hitzig zones (tip of nose, band including nipple area, medial forearms, and lateral leg)
- Can present with Charcot foot and, rarely, recurrent abdominal pain
- Diagnosed by serum CMIA, but RPR may be negative
Others
- Isolated ocular neurosyphilis
- Meningitis: can present at any time during the course of disease
- Others
Cardiovascular Syphilis
- Occurs in 10% of people with untreated syphilis
- Incubation period is 20-25 years
- Aortic root involvement leading to aortitis and dilatation
- May result in aneurysm, aortic insufficiency, or angina secondary to stenosis at the aortic root
- Diagnosed by RPR +/- CMIA
Gummatous Syphilis
- Gummas are necrotizing granulomatous lesions
- Occurs in 15% of people with untreated syphilis
- Incubation period 6-8 years
- Gummas may appear anywhere, in any organ, but most commonly on the skin, on mucosa, and in bones
- CNS lesions look like toxo, so beware in HIV patients
Other Presentations
- Isolated auditory syphilis
- Isolated optic syphilis
Diagnosis
- Often done as non-treponemal test to screen, followed by treponemal test to confirm
- In Ontario, we do a treponemal test to screen (CMIA), then repeat it with a more specific treponemal test (TPPA) alongside RPR
Direct Visualization
- Darkfield microscopy
- Chancre cleaned and smear obtained
- Smear must be visualized immediately
- Sensitivity decreases with duration
- Smear for fluorescent monoclonal antibody
- Best to use in primary syphilis
Non-Treponemal Tests (VDRL/RPR)
- Veneral Diseases Research Laboratory (VDRL) has been replaced by the rapid plasma reagin (RPR) test
- Quantitative tests for a non-specific anti-cardiolipin antibody that is produced in syphilitic (and other) infections
- False positives:
- Acute biologic false positive: malaria, brucellosis, and mononucleosis; maybe pregnancy
- Chronic biologic false positive: lupus and other autoimmune disorders, HIV, intravenous drug use, and leprosy
- Only 50% sensitive in primary, 100% sensitive in secondary
- Tests will eventually become nonreactive
Treponemal Tests
- More specific and sensitive, but more expensive
- False positives: lupus and other autoimmune disorders, Lyme disease, and other treponemal infections
- Remain positive for life
- Four main tests:
- Fluorescent treponemal antibody absorption (FTA-Abs): Essentially the gold standard
- Chemoluminescnence microparticle immunoassay (CMIA or CLIA): the screening test used in Ontario. Often used as a screening test as it is an easily-automated immunoassay and is more sensitive and specific than RPR.
- Treponema pallidum Particulate Agglutination assay (TPPA): a modification of the TPHA. Used as the confirmatory test (alongside RPR) used in Ontario.
- T. pallidum hemagglutination assay (TPHA): very old test.
- T. pallidum enzyme immunassay (TP-EIA)
Interpretation of Serology
CMIA screen | RPR | TPPA | Interpretation |
---|---|---|---|
Non-reactive | — | — | Negative result; or early syphilis (consider repeat in 4 weeks) |
Reactive | Reactive | Reactive | Recent or prior syphilis infection |
Reactive | Non-reactive | Reactive | Recent or prior syphilis infection |
Reactive | Non-reactive | Non-reactive | False positive; or early syphilis, previously treated, or late latent (repeat in 4 weeks) |
Reactive | Non-reactive | Indeterminate | Inconclusive result; false positive, early syphilis, old treated syphilis, or old untreated syphilis (repeat in 4 weeks) |
Reactive | Reactive | Non-reactive | Inconclusive result; false positive, early syphilis, old treated syphilis, or untreated syphilis (repeat in 4 weeks) |
Reactive | Reactive | Indeterminate | Recent or prior syphilis infection |
Lumbar Puncture for CSF
- Should be done routinely when:
- Neurological (including optic and auditory) signs or symptoms
- Failure of serologic response
- Tertiary syphilis
- Congenital syphilis
- In patients with HIV:
- CD4 ≤350
- RPR ≥1:32
- The sample should be sent for cell count and differential, protein, and either VDRL (not RPR) or FTA-Abs
Management
Primary, Secondary, and Early Latent
- Benzathine penicillin G 2.4 million units IM once, divided between two buttocks
- Alternative (penicillin allergy): doxycycline 100mg BID for 2 weeks
- Alternative (penicillin allergy and pregnancy): penicillin desensitization or azithromycin
Late Latent and Tertiary (excluding neurosyphilis)
- Benzathine penicillin G 2.4 million units IM q1week for 3 weeks
- Alternative (penicillin allergy): doxycycline for 30 days
- Monitor response with RPR titres, which should drop 4-fold within 6 months
Tertiary Neurosyphilis
- Penicillin G 4 million units IV q4h for 10 to 14 days
- Often followed by at least one dose of IM benzathine penicillin, sometimes weekly for 2-3 weeks
Congenital Syphilis
- If <1 month of age: crystalline penicillin G 50 kU/kg IV q12h for the first week of life and q8h thereafter, for a total of 10 days
- If ≥1 month of age: crystalline penicillin G 50,000 units/kg IV every 6 hours for 10-14 days
- If there is no neurological involvement, then you can consider benzathine penicillin G 50 kU/kg (max 2.4 MU) IM weekly for 3 weeks