introduction

  • >100 people diagnosed/yr in NZ

  • most infectious in earlier stages

  • incidence increased dramatically over last decade

  • caused by spiral shaped spirochete treponema pallidum

  • highly infectious 1ary and 2ary stages

    • able to pass through intact mucous membranes and compromised skin

    • transmissible via kissing and vaginal, oral and anal sex

    • consistent condom use reduces but doens’t elimate risk of syphilis infection

    • rate of transmisison = 30% in primary / secondary

symptoms

Primary

  • time between infection and initial symptoms average 21d (10-90)

  • appearance of single chancre (although multiple lesions may occur)

    • firm, painless and can vary in size up to \~3cm

    • appears at site of disease transmission

      • therefore may not be noticed
    • non tender lymphadenopathy may develop near site of chancre

  • usually resolves wihin 4-8 weeks and doesn’t required localised treatment

  • antibiotic treatment to prevent syphilis infection from progression

  • atypical presentation:

    • multiple or painful ulcers

Secondary

  • develops 3w - 3m after appearance of primary syphilis

    • if left untreated
  • characterised by skin rashes and mucous membrane lesions

    • typcial rash

    • widespread

    • symmetrical eruption

      • slighly scaly

      • reddish brown plaques

      • occur palms and soles

    • rashes non specific

    • may resemble pityriasis rosea for example

    • may be faint so not noticed

  • Comdylomata lata may aloso be present

    • moist

    • grey, pink or white

    • raised wart-like lesions/plaques

    • highly infectious areas of concentrated spirochete particulates

    • occur penis,vulva,rectum,mouth,throat,larynx,innerthighs,armpits, under breasts

  • Other symptoms;

    • flu-like

    • lymphadenopathy

    • triedness

    • heaache

    • sore throat

    • fever

    • weight loss

  • rashes and lesions usually resolve within 2-6w

  • antibiotic treatmetn reduces duration of symptoms and prevents progression

Tertiary

  • following aymptomatic latent period

    • may last > decade
  • infectivity waning

  • 1/3 of untreated will devleop 3ary syphilis

  • infection identifiable on serological testing

  • 3-10yr after first contracted

    • can appear up to 40 yrs later
  • Neurological

    • Neurosyphilis

      • numbness in arms, legs, face

      • paralysis

      • gradual blindness

      • changes in mental state

      • dementia

  • Cardiovascualr

    • chornic inflmamation of aorta

      • aneurysm formation

      • aortic valve incometence

      • CHF

    • Granulomatous lesions (gummas)

      • painless rubbery nodules seen skin, mouth,throat

      • may ulcerate

      • form as lesions in long bones

      • bone pain @ night

Congential syphilis

  • infection passed vertically from mother to infant

  • risk \~ 75-95%

    • in mother with 1ary syphilis
  • risk of mother passing infection remains up to 7 years psot infection ifuntreated

  • doens’t need to be symptomatic to pass on

  • serology testing for syphilis included in first antentaal screen

  • should be repeated @ 28w and prior to delivery with high risk of syphilis infection

    • recent immigrants from high risk countries

Testing

  • two types of serology

    • non-specific (non-treponemal)

      • RPR, VDRL

        • high false positive

        • esp in women who are pregnant, cancer, autoimmune, co-morbid viral infections, older people and in people who use illicit drugs

    • specific (treponemal)

      • low false positive

      • enzyme immunoassay first

        • if posiive then

        • TTPA

          • treponemal pallidum particle agglutination
    • disease activity determined using RPR

  • “syphillis serology”

Intepretation:

| EIA | TPPA | RPR | Intepretation |

| === | ===| ===|===|

| NR | Not tested | not tested | no evidence of syphilis, too early, retest 1/12 |

| R | NR | NR | Possible early primary, latent or false pos; retest 1/12 |

| R | NR | R | Probable early primary, false + possible but unlikely; retest 2w |

| R | R | NR | evidence of past infection/possible latent infection |

| R | R | R | current syphilis |

| R = reactive, NR = Non reactive |\|\|\|

Management

  • all patients with suspected syphilis referred to, or discussed with, specialist sexual health service

  • Benzathine benzylpenicillin = first line treatment

  • macrolides/cephalosporin alternative

  • Effective treatment usually results in decline in RPR titres

  • return to pre0infective levels may take years

  • Jarisch-Herxheimer reaction

    • worsening of rash and fever, headahce, malaise, myalgia after administration of abx

    • not important unless:

      • neurological/opthalmic involvment

      • occurs in pregnancy

      • common secondary syphilis

      • release of endotoxins from dying spirochaetes