Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1999 Apr;12(2):187-209.
doi: 10.1128/CMR.12.2.187.

Syphilis: review with emphasis on clinical, epidemiologic, and some biologic features

Affiliations
Review

Syphilis: review with emphasis on clinical, epidemiologic, and some biologic features

A E Singh et al. Clin Microbiol Rev. 1999 Apr.

Abstract

Syphilis is a chronic disease with a waxing and waning course, the manifestations of which have been described for centuries. It occurs worldwide, and the incidence varies significantly with geographic location. Transmission is mainly by sexual contact. The causative organism, Treponema pallidum, was first described in 1905, but because of the inability to culture the organism and the limitations of direct microscopy, serologic testing is the mainstay of laboratory diagnosis. The disease has been arbitrarily divided into several stages. The primary stage is defined by a chancre at the site of inoculation. The secondary stage is characterized by a polymorphic rash, lymphadenopathy, and other systemic manifestations. A variable asymptomatic latent period follows, which for epidemiologic purposes is divided into early (<1 year) and late (>1 year) stages. The early stages (primary, secondary, and early latent) are potentially infectious. The tertiary stage is the most destructive and is marked by cardiovascular and neurologic sequelae and gummatous involvement of any organ system. Congenital infection may result in protean early or late manifestations. Unlike many other bacteria causing infectious diseases, the organism remains sensitive to penicillin, and this remains the mainstay of therapy.

PubMed Disclaimer

References

    1. Abell E, Marks R, Jones E W. Secondary syphilis: a clinico-pathological review. Br J Dermatol. 1975;93:53–61. - PubMed
    1. Alder J, Jarvis K, Mitten M, Shipkowitz N L, Gupta P, Clement J. Clarithromycin therapy of experimental Treponema pallidum infections in hamsters. Antimicrob Agents Chemother. 1993;37:864–867. - PMC - PubMed
    1. Alexander L J, Schoch A G. Prevention of syphilis. Arch Dermatol Syphilol. 1949;59:1–10. - PubMed
    1. Ali Z. Resurgence of congenital syphilis in Trinidad. J Trop Pediatr. 1990;36:104–108. - PubMed
    1. Anderson J, Mindel A, Tovey S J, Williams P. Primary and secondary syphilis, 20 years’ experience. 3. Diagnosis, treatment, and follow up. Genitourin Med. 1989;65:239–243. - PMC - PubMed