皮肤纤毛囊肿:2 个病例报告和文献综述。

IF 1.1 4区 医学 Q4 DERMATOLOGY
American Journal of Dermatopathology Pub Date : 2024-11-01 Epub Date: 2024-06-28 DOI:10.1097/DAD.0000000000002777
Anıl Can Yalçın, Nazlıcan Yalçın, Halil İbrahim Çakmak, Recep Bedir
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引用次数: 0

摘要

摘要:皮肤纤毛囊肿是一种罕见的良性病变,最常见于年轻女性患者的下肢。关于这些囊肿的起源仍存在争议,最常见的理论是穆勒氏异位症和肾上腺化生。为了进一步扩大资料库,我们新增了 2 例皮肤纤毛囊肿病例,并收集了全部 67 例文献资料。我们想强调的是,免疫组化和人口统计学信息在区分这种囊肿的两种可能起源方面可能起着关键作用,即雌激素受体、孕酮受体和癌胚抗原免疫组化。雌激素受体和孕酮受体核阳性可证明囊肿来源于穆勒氏腺,但如果雌激素受体和孕酮受体核阴性,而癌胚抗原阳性,则最有可能是肾上腺化生。我们主张使用 "皮肤穆勒氏囊肿 "和 "纤毛皮肤蜕膜囊肿 "来代替 "皮肤纤毛囊肿",以准确说明它们的不同起源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cutaneous Ciliated Cysts: 2 Case Reports and Review of Literature.

Abstract: Cutaneous ciliated cysts are rare benign lesions most commonly seen in the lower extremities of young female patients. There is still ongoing debate about the origin of these cysts, with the most common theories being Mullerian heterotopia and eccrine gland metaplasia. To further increase the data pool, we present 2 new cutaneous ciliated cyst cases and gathered data about all 67 cases of literature. We want to highlight that immunohistochemistry and demographic information may play a key role in distinguishing between the 2 possible origins of this cyst, namely estrogen receptor, progesterone receptor, and carcinoembryonic antigen immunohistochemistry. Estrogen receptor and progesterone receptor nuclear positivity is proof of Mullerian origin, but when they are negative with a positive carcinoembryonic antigen, the most likely origin is eccrine gland metaplasia. We advocate using the terms "Cutaneous Mullerian Cyst" and "Ciliated Cutaneous Eccrine Cyst" instead of "Cutaneous Ciliated Cyst" to accurately indicate their distinct origins.

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来源期刊
CiteScore
1.80
自引率
9.10%
发文量
453
审稿时长
3 months
期刊介绍: The American Journal of Dermatopathology offers outstanding coverage of the latest diagnostic approaches and laboratory techniques, as well as insights into contemporary social, legal, and ethical concerns. Each issue features review articles on clinical, technical, and basic science advances and illuminating, detailed case reports. With the The American Journal of Dermatopathology you''ll be able to: -Incorporate step-by-step coverage of new or difficult-to-diagnose conditions from their earliest histopathologic signs to confirmatory immunohistochemical and molecular studies. -Apply the latest basic science findings and clinical approaches to your work right away. -Tap into the skills and expertise of your peers and colleagues the world over peer-reviewed original articles, "Extraordinary cases reports", coverage of practical guidelines, and graphic presentations. -Expand your horizons through the Journal''s idea-generating forum for debating controversial issues and learning from preeminent researchers and clinicians
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