一个非常罕见的位置皮肤纤毛囊肿在一个16个月大的女性:一个病例报告。

Q3 Medicine Acta medica academica Pub Date : 2022-12-01 DOI:10.5644/ama2006-124.390
Michail Anastasakis, Ioanna Gkalonaki, Charalampos Doitsidis, Ioannis Patoulias
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引用次数: 0

摘要

目的:工作的目的是显示皮肤纤毛囊肿(CCC)在一个不寻常的位置在一个16个月大的女孩。病例报告:我们提出的情况下,16个月健康的女孩提出了我们的医院,报告可触及的肿块在左侧肩胛上区域。体格检查显示一个质地柔软、上下波动、可移动、无痛的实体,没有进一步的局部炎症迹象。为了诊断和治疗目的,在全身麻醉下完全切除肿块。根据组织病理学结果,囊性病变被假层状纤毛上皮覆盖,类似于正常输卵管的上皮,被平滑肌层包围。免疫组化研究发现囊肿上皮细胞角蛋白(CKAE1/AE3)表达,尽管雌激素和孕激素受体免疫染色结果为阴性。结论:我们的病例报告涉及一个不寻常的位置,在肩胛上区域的CCC。在对国际文献进行全面回顾后,我们得出结论,这是关于该特定地点的第二个已发表的病例。据我们所知,这位患者是有史以来最年轻的CCC确诊患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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A Remarkably Rare Position of a Cutaneous Ciliated Cyst in a 16 Month-old Female: A Case Report.

Objective: The aim of the work was to show a Cutaneous Ciliated Cyst (CCC) in an unusual location in a 16-month-old girl.

Case report: We present the case of a 16-month otherwise healthy girl presented to our hospital, with a report of a palpable mass in the left suprascapular region. Physical examination revealed a soft-textured, fluctuating, mobile and painless entity, with no further indications of local inflammation. The mass was totally excised, under general anesthesia, for both diagnostic and therapeutic purposes. According to the histopathological findings, the cystic lesion was covered by a pseudostratified ciliary epithelium, resembling the epithelium of a normal fallopian tube, surrounded by a smooth muscle layer. Immunohistochemical studies identified the cyst epithelium as having cytokeratin (CKAE1/AE3) expression, despite the negative immunostaining findings on Estrogen and Progesterone Receptors.

Conclusion: Our case report concerns a CCC in an unusual position, in the suprascapular area. After a thorough review of the international literature, we concluded that this is the second published case regarding this specific location. To our knowledge our patient is the youngest ever diagnosed with CCC.

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来源期刊
Acta medica academica
Acta medica academica Medicine-Medicine (all)
CiteScore
1.90
自引率
0.00%
发文量
21
审稿时长
15 weeks
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