一例鼻腔胶质异位症,可误诊为星状花纹硬化性纤维瘤/胶原瘤。

IF 1.1 Q4 PATHOLOGY
Fatma Gundogdu, Deniz Ates Ozdemir, Ibrahim Vargel
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引用次数: 0

摘要

摘要鼻胶质瘤又称鼻胶质异位症,是一种罕见的肿瘤样病变,通常发生在新生儿或婴儿身上,没有遗传倾向:病例报告:一名 4 岁儿童自出生起鼻背就长有赘生物,被诊断为鼻胶质异位症/鼻胶质瘤。病变呈硬化性纤维瘤/胶原瘤样星状形态,内含胶质组织,S100 和 GFAP 阳性:结论:当鼻背活组织检查显示硬化性显微镜检查结果并伴有storiform模式时,在做出富胶原组织谱(胶原瘤或Gardner纤维瘤)的诊断之前,应考虑鼻胶质瘤,并应要求进行免疫组化检查,以证明存在未被识别的光镜下可见的胶质成分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Case of Nasal Glial Heterotopia That Can Be Misdiagnosed as Storiform Patterned Sclerotic Fibroma/Collagenoma.

Objective: Nasal glioma, also known as nasal glial heterotopia, is a rare tumor-like lesion that often affects newborns or infants with no hereditary predisposition.

Case report: A 4-year-old child with a growth on the nasal dorsum since birth was diagnosed with nasal glial heterotopia/nasal glioma. The lesion showed a sclerotic fibroma/collagenoma-like storiform pattern with entrapped glial tissue that was S100 and GFAP positive.

Conclusion: When a biopsy of the nasal dorsum demonstrates sclerotic microscopic findings with a storiform pattern, nasal glioma should be considered before making a diagnosis in the collagen-rich tissue spectrum (collagenoma or Gardner's fibroma), and an immunohistochemical panel should be requested to demonstrate the presence of an unrecognized light microscopically visible glial component.

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来源期刊
CiteScore
1.90
自引率
10.00%
发文量
23
审稿时长
14 weeks
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