难以捉摸的四肢:一种乳外帕杰特病病例
Shalini Radhakrishnan1, Saraswathy Sreeram2, Kashinath Nayak3
1Department of Pathology, Kasturba Medical College, Mangalore, Manipal Academy of Higher Education, Manipal, Karnataka, India.
BMJ case reports
|January 8, 2024
概括
乳外帕杰特病是一种罕见的皮肤疾病,在老年男性中可以呈现为持续的,的围病变. 组织病理学检查对于初步治疗失败时的准确诊断至关重要.
科学领域:
- 皮肤病学 皮肤病学
- 在瘤学瘤学.
背景情况:
- 乳外帕杰特病 (EMPD) 是一种罕见的模仿帕杰特病的病症,通常会影响阴阴部和部.
- 它通常呈现为非特异性,发和红血性病变,可能导致诊断延迟.
研究的目的:
- 突出考虑EMPD在老年患者中具有不响应的围病变的重要性.
- 在模糊的皮肤病例中强调组织病理学检查的诊断作用.
主要方法:
- 一个老年男性的病例介绍,他有3个月的性,红血性,周病变的病史.
- 病变的活检用于组织病理学检查以确认诊断.
主要成果:
- 患者的病变通过组织病理学被诊断为乳腺外帕杰特病.
- 病变没有响应最初的抗真菌治疗,强调需要进一步调查.
结论:
- 对EMPD的认识对于出现非特异性,耐治疗的围病变的老年人来说至关重要.
- 组织病理学检查对于明确诊断像EMPD这种模两可的病例至关重要.
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