SYPHILIS

Syphilis is caused by infection, through abrasions in the skin or
mucous membranes, with the spirochaete Treponema pallidum.
In adults the infection is usually sexually acquired; however,
transmission by kissing, blood transfusion and percutaneous injury
has been reported. Transplacental infection of the fetus can occur
The natural history of untreated syphilis is variable. Infection may remain
latentthroughout, or clinical features may develop at any time. All infected
patientsshould be treated. Penicillin remains the drug of choice for all stages
of infection.

CLASSIFICATION OF SYPHILIS

Stage
1- Acquired

Early Primary
Secondary
Latent

Late
Latent
Benign tertiary
Cardiovascular
Neurosyphilis

2- congenital

Early Clinical and latent

Late
Clinical and latent

ACQUIRED SYPHILIS

Early syphilis

Primary syphilis


The incubation period is usually between 14 and 28 days with a range of 9-90
days.The primary lesion or chancre develops at the site of infection, usually in
the genital area. A dull red macule develops, becomes papular and then erodes
to form an induratedulcer (chancre). The draining inguinal lymph nodes may
become moderately enlarged,mobile, discrete and rubbery. The chancre and
the lymph nodes are both painless andnon-tender, unless there is concurrent
or secondary infection. Without treatment, thechancre will resolve within 2-6
weeks to leave a thin atrophic scar.
Chancres may develop on the vaginal wall and on the cervix. Extragenital chancres
arefound in about 10% of patients, affecting sites such as the finger, lip, tongue,
tonsil, nipple,anus or rectum. Anal chancres often resemble fissures and may be
painful.

Secondary syphilis

This occurs 6-8 weeks after the development of the chancre when treponemes
disseminateto produce a multisystem disease. Constitutional features such as
mild fever, malaise andheadache are common. Over 75% of patients present
with a rash on the trunk and limbsthat may later involve the palms and soles;
this is initially macular but evolves to maculo-papular or papular forms, which
are generalised, symmetrical and non-irritable. Scales may form on the papules
later. Without treatment, the rash may last for up to 12 weeks. Condylomata
lata (papules coalescing to plaques) may develop in warm, moist sites such
as the vulva or perianal area. Generalised non-tender lymphadenopathy is present
inover 50% of patients. Mucosal lesions, known as mucous patches, may affect
the genitalia,mouth, pharynx or larynx and are essentially modified papules, which
become eroded.Rarely, confluence produces characteristic 'snail track ulcers' in the
mouth.

Other features such as meningitis, cranial nerve palsies, anterior or posterior uveitis,
hepatitis, gastritis, glomerulonephritis or periostitis are sometimes seen.
The differential diagnosis of secondary syphilis can be extensive, but in the context
of a -suspected STI, primary HIV infection is the most important alternative condition
to consider

Latent syphilis

This phase is characterised by the presence of positive syphilis serology or the diagnostic cerebrospinal fluid (CSF) abnormalities of neurosyphilis in an untreated patient with no
evidence of clinical disease. It is divided into early latency (within 2 years of infection), when syphilis may be transmitted sexually, and late latency, when the patient is no longer sexually infectious. Transmission of syphilis from a pregnant woman to her fetus, and rarely by blood transfusion, is possible for several years following infection.

Late syphilis

Late latent syphilis

This may persist for many years or for life. Without treatment over 60% of patients might
be expected to suffer little or no ill health. Coincidental prescription of antibiotics for other
illnesses such as respiratory tract or skin infections may treat latent syphilis serendipitously.

Benign tertiary syphilis

This may develop between 3 and 10 years after infection but is now rarely seen in the UK.
Skin, mucous membranes, bone, muscle or viscera can be involved. The characteristic feature
is a chronic granulomatous lesion called a gumma, which may be single or multiple. Healing
with scar formation may impair the function of the structure affected. Skin lesions may take
the form of nodules or ulcers whilst subcutaneous lesions may ulcerate with a gummy
discharge. Healing occurs slowly with the formation of characteristic tissue paper scars.
Mucosal lesions may occur in the mouth, pharynx, larynx or nasal septum, appearing as punched-out ulcers. Of particular importance is gummatous involvement of the tongue,
healing of which may lead to leucoplakia with the attendant risk of malignant change.
Gummas of the tibia, skull, clavicle and sternum have been described, as has involvement
of the brain, spinal cord, liver, testis and, rarely, other organs. Resolution of active disease
should follow treatment, though some tissue damage may be permanent. Paroxysmal cold haemoglobinuria .
  • birth of a baby with latent infection who either remains well or develops congenital syphilis/stigmata later in life .

  • Investigations in adult cases

    SEROLOGICAL TESTS FOR SYPHILIS

    Non-treponemal (non-specific) tests
    • Venereal Diseases Research Laboratory (VDRL) test
    • Rapid plasma reagin (RPR) test
    Treponemal (specific) antibody tests

    • Treponemal antigen-based enzyme immunoassay (EIA) for IgG and IgM
    • T. pallidum haemagglutination assay (TPHA)
    • T. pallidum particle agglutination assay (TPPA)
    • Fluorescent treponemal antibody-absorbed (FTA-ABS) Test

    Investigations in suspected congenital syphilis

    Passively transferred maternal antibodies from an adequately treated mother may
    give rise to positive serological tests in her baby. In this situation, non-treponemal tests
    should become negative within 3-6 months of birth. A positive EIA test for antitreponemal
    IgM suggests early congenital syphilis. A diagnosis of congenital syphilis mandates
    investigation of the mother, her partner and any siblings.

    Management

    Penicillin is the drug of choice. Specific regimens depend on the stage of infection. Longer
    courses are required in late syphilis and in HIV co-infection. Doxycycline is indicated for
    patients allergic to penicillin, except in pregnancy (see below). Azithromycin has also been advocated, but recent outbreaks in UK cities have been associated with strains of
    T. pallidum such as Street 14 that are resistant to macrolides. All patients must be
    followed up to ensure cure, and partner notification is of particular importance.
    Resolution of clinical signs in early syphilis with declining titres for non-treponemal tests,
    usually to undetectable levels within 6 months for primary syphilis and 12-18 months for secondary syphilis, are indicators of successful treatment. Specific treponemal antibody
    tests may remain positive for life. In patients who have had syphilis for many years there
    may be little serological response following treatment.

    Pregnancy

    Penicillin is the treatment of choice in pregnancy. Erythromycin stearate can be given if
    there is penicillin hypersensitivity, but crosses the placenta poorly; the newborn baby
    must therefore be treated with a course of penicillin and consideration given to retreating
    the mother. Some specialists recommend penicillin desensitisation for pregnant mothers
    so that penicillin can be given during temporary tolerance. The author has successfully
    prescribed ceftriaxone 250 mg i.m. for 10 days in this situation. Babies should be treated in hospital with the help of a pediatrician.
    .

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