An Adolescent Female With Concurrent Presentation of Autoimmune Hepatitis and Secondary Syphilis.

JPGN reports Pub Date : 2023-11-27 eCollection Date: 2023-11-01 DOI:10.1097/PG9.0000000000000382
Madison Riddell, Chris Novak, Sarah Dinn, Gary Galante
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Abstract

We describe concurrent diagnoses of autoimmune hepatitis (AIH) and secondary syphilis in a 17-year-old adolescent with jaundice, with possible syphilitic hepatitis (SH) excluded after a thorough investigation. Our patient presented with a several-day history of malaise, progressive jaundice, and vomiting. She disclosed being sexually active and requested testing for sexually transmitted infections. Her subsequent investigations demonstrated acute hepatitis with a positive antinuclear antibody and elevated IgG. She also tested positive for syphilis with a reactive rapid plasma regain and treponema pallidum particle agglutination assay. We considered 2 etiologies for her elevated liver enzymes: syphilitic hepatitis and AIH. AIH was confirmed on liver biopsy, establishing the first reported pediatric case of concurrent AIH and secondary syphilis. Syphilis is hypothesized to be an infectious trigger for AIH.

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同时出现自身免疫性肝炎和继发性梅毒的青春期女性。
我们描述了一名17岁青少年黄疸并发自身免疫性肝炎(AIH)和继发性梅毒的诊断,在彻底调查后排除了可能的梅毒肝炎(SH)。我们的病人有几天的不适史,进行性黄疸和呕吐。她透露自己性活跃,并要求进行性传播感染检测。随后的调查显示她患有急性肝炎,抗核抗体阳性,IgG升高。她还通过反应性快速血浆恢复和梅毒螺旋体颗粒凝集试验检测梅毒呈阳性。我们考虑了她肝酶升高的两种病因:梅毒肝炎和AIH。肝活检证实AIH,建立了第一例报道的儿童AIH并发继发性梅毒病例。梅毒被认为是AIH的传染性诱因。
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