Severe Rectal Syphilis in the Setting of Profound HIV Immunosuppression: A Case Report Highlighting ERG/CD38 Immunophenotyping and a Review of the Literature.

IF 3.4 Q2 INFECTIOUS DISEASES
Diana Marcela Carmona Valencia, Juan Diego López, Shirley Vanessa Correa Forero, Diana Marcela Bonilla Bonilla, Jorge Karim Assis, Yamil Liscano
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引用次数: 0

Abstract

Background and Aim: Syphilis, caused by Treponema pallidum, classically presents with genital or anal chancres; rectal involvement is rare and frequently misdiagnosed as inflammatory bowel disease or malignancy. We describe an unusually severe case of syphilitic proctitis in the setting of advanced HIV-related immunosuppression (CD4 39 cells/µL), in which targeted immunophenotyping (ERG and CD38) was a valuable adjunctive tool in the differential diagnosis. Case Presentation: A 46-year-old man with a recent history of erosive gastritis and esophageal candidiasis presented after six months of unintentional 20 kg weight loss, profound fatigue, intermittent fevers, profuse diarrhea, and two episodes of hematemesis. Workup revealed a new diagnosis of HIV infection (CD4: 39 cells/µL; viral load: 87,837 copies/mL). Contrast-enhanced CT demonstrated uniform, concentric rectal wall thickening ("target sign"). Colonoscopic biopsy showed exuberant granulation tissue and dense plasma cell infiltrates. Immunohistochemistry revealed a dense infiltrate of CD38-positive plasma cells and ERG-positive endothelial proliferation. These findings, in the context of positive serology, were highly supportive of a spirochetal etiology and helped differentiate it from potential mimics. Serology was positive for latent late syphilis (VDRL 1:64). The patient received three weekly doses of intramuscular benzathine penicillin; lumbar puncture excluded neurosyphilis. Discussion: This is among the first reported cases of syphilitic proctitis in a patient with CD4 < 50 cells/µL, where advanced immunophenotyping differentiated syphilitic inflammation from neoplastic or inflammatory mimics. Profound immunosuppression accelerates disease progression and yields atypical clinical features. Conclusion: In HIV-infected patients with chronic rectal symptoms, especially those with CD4 < 50 cells/µL, syphilitic proctitis must be considered. Integration of radiologic assessment, histopathology with ERG/CD38 staining, and serologic testing permits prompt diagnosis. Early benzathine penicillin therapy and rigorous clinical and serologic follow-up are essential to prevent complications, including neurosyphilis.

HIV免疫抑制环境下的严重直肠梅毒:1例强调ERG/CD38免疫表型的病例报告和文献综述
背景与目的:梅毒由梅毒螺旋体引起,典型表现为生殖器或肛门病变;直肠受累是罕见的,经常误诊为炎症性肠病或恶性肿瘤。我们描述了一个异常严重的梅毒直肠炎病例,在hiv相关免疫抑制(CD4 39细胞/µL)的背景下,靶向免疫分型(ERG和CD38)是鉴别诊断中有价值的辅助工具。病例介绍:一名46岁男性,近期有糜烂性胃炎和食道念珠菌病病史,6个月后出现体重减轻20公斤、极度疲劳、间歇性发热、大量腹泻和两次吐血。复查发现新诊断HIV感染(CD4: 39个细胞/µL;病毒载量:87,837拷贝/mL)。增强CT显示直肠壁均匀、同心增厚(“靶征”)。结肠镜活检显示大量肉芽组织和致密浆细胞浸润。免疫组化示cd38阳性浆细胞密集浸润,内皮细胞erg阳性增生。在阳性血清学背景下,这些发现高度支持螺旋体病因学,并有助于将其与潜在的模仿物区分开来。血清潜伏性晚期梅毒阳性(VDRL 1:64)。患者每周接受三次肌注苄星青霉素;腰椎穿刺排除神经梅毒。讨论:这是首例报道的CD4 < 50细胞/µL的梅毒直肠炎患者,其中晚期免疫表型将梅毒炎症与肿瘤或炎症模拟区分开来。深度免疫抑制加速疾病进展并产生非典型临床特征。结论:在出现直肠慢性症状的hiv感染者中,特别是CD4 < 50 cells/µL者,必须考虑梅毒性直肠炎。结合放射学评估、ERG/CD38染色的组织病理学和血清学检测,可以及时诊断。早期苄星青霉素治疗和严格的临床和血清学随访对于预防并发症(包括神经梅毒)至关重要。
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来源期刊
Infectious Disease Reports
Infectious Disease Reports INFECTIOUS DISEASES-
CiteScore
5.10
自引率
0.00%
发文量
82
审稿时长
11 weeks
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