Suppr超能文献

伴有腹股沟淋巴结病的包皮坏死性肉芽肿性肿块:梅毒的一种罕见表现。

Necrotising granulomatous mass of the foreskin with inguinal lymphadenopathy: a rare presentation of syphilis.

作者信息

Pham Cecile, Wang Luke, Lea Vivienne, Rathore Prem

机构信息

Urology, Campbelltown Hospital, Campbelltown, New South Wales, Australia

Urology, Campbelltown Hospital, Campbelltown, New South Wales, Australia.

出版信息

BMJ Case Rep. 2021 Mar 10;14(3):e238539. doi: 10.1136/bcr-2020-238539.

Abstract

We report the case of a 24-year-old man who presented with a 5-week history of painful right inguinal lymphadenopathy, weight loss and non-ulcerative foreskin mass. The patient's symptoms progressed despite initial antibiotic therapy. The foreskin mass was clinically suspicious for squamous cell carcinoma; however, histopathology of both the foreskin mass and inguinal lymph node showed necrotising granulomatous inflammation. Extensive immunohistochemistry testing was inconclusive and could not identify a causative microorganism. Ultimately, serology was positive for and he was treated with intramuscular benzathine penicillin. This is an unusual case, which highlights the importance of extensive investigation for differential diagnoses of penile mass and exemplifies the resurgence of syphilis in developed countries.

摘要

我们报告了一例24岁男性病例,该患者有5周的右侧腹股沟淋巴结疼痛、体重减轻及非溃疡性包皮包皮包皮淋巴结肿大病史。尽管最初进行了抗生素治疗,患者症状仍进展。包皮肿物临床怀疑为鳞状细胞癌;然而,包皮肿物及腹股沟淋巴结的组织病理学检查均显示坏死性肉芽肿性炎症。广泛的免疫组化检测结果不明确,未能鉴定出致病微生物。最终,血清学检测梅毒螺旋体抗体呈阳性,患者接受了苄星青霉素肌内注射治疗。这是一例不寻常的病例,突出了对阴茎肿物进行广泛鉴别诊断调查的重要性,并例证了梅毒在发达国家的再度流行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86fe/7949378/a0bcbaf33350/bcr-2020-238539f01.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验