CUTANEOUS LUPUS MIMICKING SECONDARY SYPHILIS IN A PATIENT WITH POSITIVE ANTICARDIOLIPIN ANTIBODY - A CASE REPORT

CUTANEOUS LUPUS MIMICKING SECONDARY SYPHILIS IN A PATIENT WITH POSITIVE ANTICARDIOLIPIN ANTIBODY - A CASE REPORT

SILVA, CAUÊ JOSÉ PEDROSO PINHEIRO DA; DEITOS, JULIA; KUZMA, ANDRESSA CAROLINE; VILA, LUISA MANFREDIN; BALBINOT, JACKSON DANRLEI; PIENTKA, LUCAS THIESEN; ADAME, ANA PAULA; NOGUEIRA, MARCIO AUGUSTO

Pôster:

Systemic lupus erythematosus (SLE) is a chronic autoimmune disease, which etiology is not yet well understood. SLE manifests itself in various systems, such as the skin, joints, central nervous system and kidneys. Syphilis is a disease caused by Treponema pallidum infection, and it is mostly transmitted via direct contact with a syphilitic sore on the skin or mucous membranes. Both diseases, albeit different in their etiopathogenesis, can affect many systems and have similar clinical manifestations. The dermatologic findings of secondary syphilis are variable, and may mimic cutaneous lupus, which can be differentiated by biopsy of the lesion. The symptoms of malar rash and photosensitivity occur in 30-40% of SLE patients, while dermatological manifestations occur in 88-100% of cases of secondary syphilis. Non-treponemal tests to diagnosis syphilis have a high number of false-positive results, specially in patients with SLE, antiphospholipid syndrome or other diseases of the connective tissue.

Case report

A 27-year-old man presented with a 10-day history of asthenia, hyporexia, somnolence, headaches, dizziness and target-shape erythematous lesions with central paleness on the face, trunk and back, without local pain or other accompanying symptoms. Laboratory investigations revealed a VDRL titer of 1:32, and a negative FTA-Abs. Biopsy of one of the lesions was negative for syphilitic roseola. After discarding the diagnosis of secondary syphilis, the investigation for SLE was initiated. Further laboratory tests showed a positive ANA result (1:640, fine-speckled), and a reagent IgM/IgG anticardiolipin antibody, besides positive results for other autoantibodies in SLE: anti-Sm and anti-dsDNA (1:640). Based on these findings, treatment for SLE was initiated.

Conclusion

Both syphilis and SLE are referred to as “great imitators”, and physicians may consider them differential diagnosis for almost any clinical malady. Due to the similar manifestations of those disorders, biopsy of the lesions and laboratory tests are required to arrive at a definitive diagnosis. Our patient had a positive anticardiolipin antibody and dermatologic findings similar to secondary syphilis, which posed a confounding factor in the diagnosis of SLE.

Systemic lupus erythematosus (SLE) is a chronic autoimmune disease, which etiology is not yet well understood. SLE manifests itself in various systems, such as the skin, joints, central nervous system and kidneys. Syphilis is a disease caused by Treponema pallidum infection, and it is mostly transmitted via direct contact with a syphilitic sore on the skin or mucous membranes. Both diseases, albeit different in their etiopathogenesis, can affect many systems and have similar clinical manifestations. The dermatologic findings of secondary syphilis are variable, and may mimic cutaneous lupus, which can be differentiated by biopsy of the lesion. The symptoms of malar rash and photosensitivity occur in 30-40% of SLE patients, while dermatological manifestations occur in 88-100% of cases of secondary syphilis. Non-treponemal tests to diagnosis syphilis have a high number of false-positive results, specially in patients with SLE, antiphospholipid syndrome or other diseases of the connective tissue.

Case report

A 27-year-old man presented with a 10-day history of asthenia, hyporexia, somnolence, headaches, dizziness and target-shape erythematous lesions with central paleness on the face, trunk and back, without local pain or other accompanying symptoms. Laboratory investigations revealed a VDRL titer of 1:32, and a negative FTA-Abs. Biopsy of one of the lesions was negative for syphilitic roseola. After discarding the diagnosis of secondary syphilis, the investigation for SLE was initiated. Further laboratory tests showed a positive ANA result (1:640, fine-speckled), and a reagent IgM/IgG anticardiolipin antibody, besides positive results for other autoantibodies in SLE: anti-Sm and anti-dsDNA (1:640). Based on these findings, treatment for SLE was initiated.

Conclusion

Both syphilis and SLE are referred to as “great imitators”, and physicians may consider them differential diagnosis for almost any clinical malady. Due to the similar manifestations of those disorders, biopsy of the lesions and laboratory tests are required to arrive at a definitive diagnosis. Our patient had a positive anticardiolipin antibody and dermatologic findings similar to secondary syphilis, which posed a confounding factor in the diagnosis of SLE.

Palavras-chave:

DOI: 10.5151/sbr2019-069

Referências bibliográficas

• [1]

Como citar:

SILVA, CAUÊ JOSÉ PEDROSO PINHEIRO DA; DEITOS, JULIA; KUZMA, ANDRESSA CAROLINE; VILA, LUISA MANFREDIN; BALBINOT, JACKSON DANRLEI; PIENTKA, LUCAS THIESEN; ADAME, ANA PAULA; NOGUEIRA, MARCIO AUGUSTO; "CUTANEOUS LUPUS MIMICKING SECONDARY SYPHILIS IN A PATIENT WITH POSITIVE ANTICARDIOLIPIN ANTIBODY - A CASE REPORT", p-69-69. In: Anais do 36º Congresso Brasileiro de Reumatologia. [ISBN 978-85-212-1892-0]. São Paulo: Blucher, 2019.
ISSN 23577282, DOI 10.5151/sbr2019-069