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神经滤泡性错构瘤表现为一种罕见的附件肿瘤,与基底细胞癌相关。

Neurofolicullar hamartoma presenting as a rare adnexal neoplasm in association with basal cell carcinoma.

作者信息

Montazer Fatemeh, Sanei Motlagh Alireza

机构信息

Department of Pathology, Gastrointestinal Cancer Research Center, Imam Hospital, Mazandaran University of Medical Sciences, Sari, Iran.

Department of Pathology, Iran University of Medical Sciences, Tehran, Iran.

出版信息

Caspian J Intern Med. 2019 Winter;10(1):107-110. doi: 10.22088/cjim.10.1.107.

Abstract

BACKGROUND

Neurofollicular hamartoma (NFH) is characterized histopathologically by fascicles of spindle cells that laterally delimited by hyperplastic folliculosebaceous units. It usually appears on face, near the nose or nasolabial fold. It does not manifest true neural differentiation and recently the term spindle cell predominant trichodiscoma (SCPT) has been used instead.

CASE PRESENTATION

We present a case of a 40-year-old male with co-incidence of NFH and basal cell carcinoma (BCC) that the mesenchymal components of NFH were similar to SCPT but these components highly expressed S-100 protein. We also discuss about the histological aspect of the neoplasia in this report and consider the findings of other reports in association with classification of NFH by means of cellular markers and morphological resemblance to other skin hamartomas.

CONCLUSION

Neurofollicular hamartoma is a rare benign tumor that thought to represent the cellular end of a morphological spectrum with trichodiscoma. The morphological features and expression of S100 protein in neural element helped us to achieve the diagnosis of neurofollicular hamartoma. However, variable reports of S-100 protein expression in NFH are available and further studies are needed to determine the classification of this tumor.

摘要

背景

神经毛囊错构瘤(NFH)在组织病理学上的特征是梭形细胞束,其由增生的毛囊皮脂腺单位横向界定。它通常出现在面部,靠近鼻子或鼻唇沟。它不表现出真正的神经分化,最近使用了梭形细胞为主的毛发上皮瘤(SCPT)这一术语。

病例报告

我们报告一例40岁男性同时患有NFH和基底细胞癌(BCC)的病例,其中NFH的间充质成分与SCPT相似,但这些成分高表达S-100蛋白。我们还在本报告中讨论了该肿瘤的组织学方面,并通过细胞标志物以及与其他皮肤错构瘤的形态学相似性来考虑其他报告的结果,以关联NFH的分类。

结论

神经毛囊错构瘤是一种罕见的良性肿瘤,被认为代表了毛发上皮瘤形态学谱系的细胞末端。神经成分中S100蛋白的形态学特征和表达有助于我们诊断神经毛囊错构瘤。然而,关于NFH中S-100蛋白表达的报告存在差异,需要进一步研究以确定该肿瘤的分类。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3819/6386336/2fe6f8a87281/cjim-10-107-g001.jpg

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