Undiagnosed Behçet's Disease Presenting as Fournier's Gangrene in a Young Male.

Case Reports in Urology Pub Date : 2021-09-21 eCollection Date: 2021-01-01 DOI:10.1155/2021/6626909
Jasmine C Winyard, Anton Wong, Hala Rashed, John K Mellon
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引用次数: 1

Abstract

Behçet's disease is rare, especially in the paediatric population. In this case, a healthy 16-year-old made presented with discrete scrotal ulcers and systemic illness. He was found to have Fournier's gangrene and with subsequent investigation was diagnosed with Behçet's disease as an underlying cause. A PubMed search reveals no similar case reports. His only risk factors for Fournier's gangrene was his raised body mass index. His only risk factor for Behçet's disease was his ethnic origin. An understanding of risk factors and epidemiology can raise suspicion of these rare pathologies.

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未确诊的behaperet病表现为富尼耶坏疽的年轻男性。
behaperet病是罕见的,特别是在儿科人群中。在这个病例中,一个健康的16岁男孩表现为离散性阴囊溃疡和全身性疾病。他被发现患有富尼耶坏疽,随后的调查被诊断为behaperet病,这是潜在的病因。PubMed搜索显示没有类似的病例报告。他患福尼耶坏疽的唯一危险因素是他的体重指数升高。他患behaperet病的唯一危险因素是他的种族血统。对危险因素和流行病学的了解可以提高对这些罕见疾病的怀疑。
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来源期刊
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0.00%
发文量
28
审稿时长
13 weeks
期刊最新文献
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