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CASE REPORT |
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Year : 2020 | Volume
: 65
| Issue : 4 | Page : 307-309 |
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Arthropod bite-like eruption as rare presentation of secondary syphilis in an HIV-infected patient |
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Chih-Yu Chen1, Yu-Hsuan Lu2, Yu-Chun Lin3, Chih-Tsung Hung1, Wei- Ming Wang1, Chien-Ping Chiang1
1 Department of Dermatology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan 2 Department of Chinese Medicine, Taipei City Hospital, Taipei, Taiwan 3 Department of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan
Date of Web Publication | 11-Jun-2020 |
Correspondence Address: Chien-Ping Chiang Department of Dermatology, Tri-Service General Hospital, National Defense Medical Center, Taipei Taiwan
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/ijd.IJD_522_18
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Abstract | | |
Secondary syphilis represents a diagnostic challenge due to its varied clinical manifestations. Co-infection with human immunodeficiency virus (HIV) adds to the diversity of the clinical presentation of syphilis. We herein report a case of secondary syphilis as an arthropod bite-like eruption in a previously undiagnosed HIV-coinfected patient. A 24-year-old homosexual male presented with multiple corticosteroid-resistant insect bite-like nodules on his trunk and bilateral arms. Skin biopsy disclosed plasma cell infiltration and positive Treponema pallidum staining. His symptoms got dramatic remission after benzathine penicillin G therapy. The presented case extends the clinical spectrum of secondary syphilis in HIV patient.
Keywords: Arthropod bite, HIV, secondary syphilis
How to cite this article: Chen CY, Lu YH, Lin YC, Hung CT, Wang W, Chiang CP. Arthropod bite-like eruption as rare presentation of secondary syphilis in an HIV-infected patient. Indian J Dermatol 2020;65:307-9 |
How to cite this URL: Chen CY, Lu YH, Lin YC, Hung CT, Wang W, Chiang CP. Arthropod bite-like eruption as rare presentation of secondary syphilis in an HIV-infected patient. Indian J Dermatol [serial online] 2020 [cited 2023 Jun 9];65:307-9. Available from: https://www.e-ijd.org/text.asp?2020/65/4/307/286403 |
Introduction | |  |
Syphilis is a sexually transmitted disease with a triphasic natural history that significantly increases susceptibility to human immunodeficiency virus (HIV) infection.[1] Known as “the great imitator,” the clinical presentation of secondary syphilis is variable, and its morphology may be atypical in patients co-infected with HIV.[2],[3] To the best of our knowledge, this is the first report of an arthropod bite-like eruption due to secondary syphilis in an HIV-infected patient.
Case History | |  |
A 24-year-old male presented with a 3-week history of numerous pruritic dull red papules and nodules on his trunk and bilateral arms [Figure 1]. No oral or genital ulcers were noted. The initial diagnosis was arthropod bite reaction. However, the eruptions were unresponsive to topical corticosteroids; therefore, a skin biopsy was conducted. | Figure 1: Multiple pruritic dull red nodules on the truck and bilateral arms. Inset shows remission of lesions after a single dose of benzathine penicillin G treatment
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Pathology revealed acanthosis with perivascular lymphoplasmacytic infiltration from superficial to deep dermis associated with interface involvement of the skin tissue [Figure 2]a and [Figure 2]b, as well as positive staining for CD138 [Figure 2]c. Immunohistochemical studies revealed the presence of Treponema pallidum in the lower mid-part of the epidermis [Figure 2]d. The patient returned to our outpatient department and admitted homosexual behavior. Laboratory results revealed rapid plasma reagin, 1:4; T. pallidum particle agglutination, 1:1280; and anti-HIV antibodies, 153.40. The final diagnosis was secondary syphilis and HIV co-infection. He received a single dose of benzathine penicillin G (2400,000 U), with almost remission of lesions [Figure 1], lower left inset]. The patient was referred to an infectious disease specialist for HIV infection control and did not experience similar symptoms during the 1-year follow-up period. | Figure 2: (a) Superficial and deep dermal infiltrate with interface involvement (H and E, ×100). (b) Perivascular lymphoplasmacytic infiltration (H and E, ×200). (c) Positive staining for CD138 highlighted the plasma cell infiltration (×200). (d) Immunohistochemical detection of Treponema pallidum (×200)
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Discussion | |  |
Syphilis is a sexually transmitted infection caused by the gram-negative bacterium, T. pallidum. It has a three-stage progression and a latent phase. Secondary syphilis occurs in approximately 25% of untreated patients, usually several weeks to a few months after the primary stage. According to the report of Centers for Disease Control and Prevention, in 2015–2016, the national rate of primary and secondary syphilis cases in the United States was 8.7 cases per 100,000 population. Secondary syphilis typically manifests with systemic symptoms such as malaise, fatigue, fever, and headache, as well as various forms of rash, which is classically a maculopapular coppery red rash diffusely involving the trunk and extremities, including the palms and soles.[4] As all of these secondary disease features are not highly suggestive of syphilis and may not be preceded by a detectable primary lesion, diagnosis of this stage of T. pallidum infection may be delayed for a long period and can easily be mistaken for another infectious or noninfectious systemic disease.[5] Chancre or typical palmoplantar rashes were not initially noted in the present case. However, numerous insect bite-like nodules were seen. According to the reported literature, this was an extremely rare presentation of secondary syphilis. Serologic testing remains the mainstay for diagnosis of syphilis because T. pallidum cannot be cultured. Nontreponemal and treponemal tests are unable to detect antibodies until the infection has progressed 1–3 weeks after the development of the chancre.[6] Direct testing methods, such as dark-field microscopic examination, direct fluorescent antibody-T. pallidum, and polymerase chain reaction, should be considered when the diagnosis of syphilis cannot be confirmed. Furthermore, skin biopsy is usually necessary to establish a diagnosis. There are some classic pathological findings in secondary syphilis, for example, the epidermis is often involved and exhibits psoriasiform hyperplasia, the dermis shows a superficial and deep chronic infiltrate, and plasma cells are present in 75% of all cases.[7] Specific Wharthin–Starry staining (silver staining) using rabbit polyclonal antibodies can be used to identify Treponema in the tissue. A single dose of benzathine penicillin G is used to treat patients with uncomplicated syphilis. HIV-infected patients, diagnosed with syphilis, do not have unique regimens but should be treated in accordance with the same recommendations as for HIV-uninfected patients. The recommended regimen for the treatment of primary and secondary syphilis in adults is benzathine penicillin G (2.4 million units IM) in a single dose, which provides at least 14 days of circulating penicillin.[6] Our case demonstrated a good response to a single dose of benzathine penicillin G and no cutaneous symptoms were noted during the 1-year follow-up period. The present case report extends the clinical spectrum of secondary syphilis in HIV patients and emphasizes the need for clinicians to have a heightened awareness of the varied and unusual clinical phenotypes of secondary syphilis in HIV-infected patients.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent form. In the form, the patient has given his consent for his images and other clinical information to be reported in the journal. The patient understands that his name and initial will not be published and due efforts will be made to conceal his identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
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5. | Cerchione C, Maraolo AE, Marano L, Pugliese N, Nappi D, Tosone G, et al. Secondary syphilis mimicking malignancy: A case report and review of literature. J Infect Chemother 2017;23:576-8. |
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7. | Engelkens HJ, ten Kate FJ, Vuzevski VD, van der Sluis JJ, Stolz E. Primary and secondary syphilis: A histopathological study. Int J STD AIDS 1991;2:280-4. |
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