罗赛-多夫曼病的鼻体表现;一个病例报告
Saad Elzayat1, Ahmed Morshedy1, Hussein A El-Shirbeny1
1Otorhinolaryngology Department, Faculty of Medicine, Kafrelsheikh University, Kafrelsheikh, Egypt.
概括
一个罕见的Rosai-Dorfman疾病 (RDD) 病例呈现为鼻质,导致鼻阻塞. 通过独特的组织病理学发现证实了诊断,包括通过切除活检,通过emperipolesis.
科学领域:
- 耳鼻喉科 耳鼻喉科 耳鼻喉科
- 病理学 病理学 病理学
- 在瘤学瘤学.
背景情况:
- 罗莎-多夫曼病 (RDD) 是一种罕见的良性增殖性疾病.
- 鼻腔阻塞可能是鼻质群体的呈现症状.
- 典型的RDD病例通常涉及宫淋巴腺病变.
研究的目的:
- 报告一个独特的呈现的罗赛-多夫曼病 (RDD) 在鼻.
- 突出RDD的诊断挑战和组织病理学特征.
- 强调活检对确定诊断的重要性.
主要方法:
- 临床检查包括鼻镜和耳部评估.
- 放射学评估. 放射学评估.
- 在全身麻醉下进行切除活检,并插入T管用于中耳输液.
- 组织病理学检查和免疫组织化学.
主要成果:
- 一名52岁的女性呈现了逐渐进展的鼻腔阻塞.
- 鼻镜检查显示出一个大,肉的,非脉动性鼻质.
- 观察到左中耳溢出;然而,没有出现宫淋巴腺病.
- 组织病理学证实了罗莎伊-多夫曼病,其特征是emperipolesis.
结论:
- 罗莎-多尔夫曼病可以不典型地呈现为鼻质,没有淋巴腺病.
- 帝国症是诊断RDD的关键组织病理特征.
- 多学科的诊断方法对于像RDD这样的罕见疾病至关重要.
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