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A 30 year old gentleman from Papua New Guinea with a history of intravenous drug use and previous imprisonment presented with a 2-week history of a non-pruritic scrotal rash. He denied any associated genitourinary, dermatological or systemic symptoms. He was an otherwise well gentleman with no significant medical history and took no regular medications. Sexual history revealed an episode of unprotected anal sex with a casual male partner 5 months prior to his presentation and four male partners in the preceding 12 months.
Examination demonstrated multiple grey papules of approximately 1 mm diameter symmetrically distributed on the scrotum. Further thorough examination was conducted to exclude secondary syphilis; regular, round brown papules were identified on the trunk, back, palms of the hands and soles of the feet, which had not been noticed by the patient (figure 1). Oral examination demonstrated grey lesions overlying the soft and hard palate suspicious for mucous patches (figure 2). There was no associated lymphadenopathy or other concerning pathology noted.
The findings were suspicious of secondary syphilis, so oral and genital lesions were sampled for nucleic acid amplification testing (NAAT) of Treponema pallidum DNA. A screen for sexually transmitted infections including HIV and syphilis was conducted. Empirical treatment with intramuscular benzathine penicillin (1.8 g) was given and the patient was advised to abstain from sex for 1 week. Both NAAT and serological assays subsequently confirmed the diagnosis of secondary syphilis with a venereal disease reference laboratory titre of 1:64. At follow-up, 1 week later, the patient’s symptoms had improved with treatment and partners from the preceding 6 months had been notified.
Syphilis, known as the ‘great imitator’, is caused by T. pallidum and is on the rise.1 Primary infection causes a, traditionally, painless, syphilitic chancre which heals within weeks and may go undetected by the patient. Haematogenous dissemination of T. pallidum occurring up to 6 months after initial infection results in secondary syphilis, which may prompt patients to seek medical attention. Dermatological manifestations of secondary syphilis can be non-specific and may present to practitioners working outside of sexual health. Condylomata lata are non-tender, moist, papules in the genital region which may be confused with genital warts. A maculopapular rash, present in up to 90% of patients, may be subtle and easily confused with pityriasis rosea, infectious mononucleosis, HIV seroconversion or drug reaction.2 3 One distinguishing feature of the rash in secondary syphilis is the involvement of the palms of the hands and soles of the feet as shown in figure 1. Mucous patches of the oral cavity are a hallmark feature of secondary syphilis and can be subtle (figure 2), being overlooked unless specifically examined for. Left untreated, secondary syphilis may lead to the complications of tertiary syphilis;1 therefore, a high index of suspicion coupled with a thorough dermatological assessment, including assessment of the palms, soles and oral cavity of patients presenting with genital lesions, is required to make the correct diagnosis.
The primary chancres of syphilis may go undetected by patients, delaying presentation until symptoms of secondary syphilis develop.
Dermatological manifestations of secondary syphilis can be non-specific and may present to practitioners working outside of sexual health.
Hallmark features of secondary syphilis include a maculopapular rash, typically affecting the palms and soles, mucous patches of the oral cavity and condylomata lata on the genital skin; examination of these areas is therefore key to clinching the diagnosis.
Contributors YH planned, designed and conducted the research contributing to this paper. She is entirely responsible for the write up and revisions.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Patient consent for publication Obtained.
Provenance and peer review Not commissioned; externally peer reviewed.
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