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头皮多发性项部纤维瘤:一例报告

Multiple nuchal-type fibromas on the scalp: a case report.

作者信息

Kim Do Hun, Kim Tae Han, Sung Nam Hee, Shin HyoSeung, Lee Ai Young, Lee Seung Ho

机构信息

Department of Dermatology, Dongguk University Ilsan Hospital, Dongguk University College of Medicine, Goyang, Korea.

出版信息

Ann Dermatol. 2015 Apr;27(2):194-6. doi: 10.5021/ad.2015.27.2.194. Epub 2015 Mar 24.

DOI:10.5021/ad.2015.27.2.194
PMID:25834360
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4377410/
Abstract

Nuchal-type fibroma is a rare, benign, fibrous, tumor-like proliferation characterized by dense hypocellular bundles of collagen, with sparsely scattered fibroblasts, interspersed fat tissue, and entrapped nerve fibers. It usually develops in the posterior neck as a solitary, firm, poorly circumscribed, subcutaneous mass. Herein, we report about a 32-year-old man who presented with a 6-year history of multiple nodules on the scalp. Histopathological features were consistent with those of nuchal-type fibroma. The tumors were surgically excised.

摘要

项部纤维瘤是一种罕见的良性纤维性肿瘤样增生,其特征为密集的低细胞性胶原束,伴有散在稀疏的成纤维细胞、散在的脂肪组织和包埋的神经纤维。它通常发生于后颈部,表现为单个、质地坚硬、边界不清的皮下肿块。在此,我们报告一名32岁男性,头皮出现多个结节已有6年病史。组织病理学特征与项部纤维瘤相符。肿瘤已通过手术切除。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceff/4377410/3db3c77e891b/ad-27-194-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceff/4377410/8adc5eaa3e90/ad-27-194-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceff/4377410/3db3c77e891b/ad-27-194-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceff/4377410/8adc5eaa3e90/ad-27-194-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceff/4377410/3db3c77e891b/ad-27-194-g002.jpg

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引用本文的文献

1
Nuchal-type Fibroma: Single-Center Experience and Systematic Literature Review.颈型纤维瘤:单中心经验和系统文献回顾。
In Vivo. 2020 Sep-Oct;34(5):2217-2223. doi: 10.21873/invivo.12032.
2
Nuchal-type fibroma of the shoulder: A case report and review of the literature.肩部项部型纤维瘤:一例病例报告及文献复习
Oncol Lett. 2016 Jun;11(6):4152-4154. doi: 10.3892/ol.2016.4530. Epub 2016 May 5.

本文引用的文献

1
Nuchal-type Fibroma of the Coccyx.尾骨部颈部型纤维瘤
Ann Dermatol. 2008 Mar;20(1):41-4. doi: 10.5021/ad.2008.20.1.41. Epub 2008 Mar 31.
2
Multiple nuchal fibromas in a 2-year-old without Gardner syndrome.一名2岁儿童患多发性颈部纤维瘤,无加德纳综合征。
Pediatr Dermatol. 2011 Nov-Dec;28(6):695-696. doi: 10.1111/j.1525-1470.2011.01415.x. Epub 2011 Sep 25.
3
Extra nuchal-type fibroma associated with elastosis, traumatic neuroma, a rare APC gene missense mutation, and a very rare MUTYH gene polymorphism: a case report and review of the literature*.
伴有弹性组织变性、创伤性神经瘤、罕见的APC基因错义突变及非常罕见的MUTYH基因多态性的额外项部型纤维瘤:1例报告并文献复习*
J Cutan Pathol. 2011 Nov;38(11):911-8. doi: 10.1111/j.1600-0560.2011.01745.x. Epub 2011 Jul 14.
4
Nuchal-type fibroma of the ankle: a case report.踝关节项圈样纤维瘤:一例报告
J Foot Ankle Surg. 2008 Jul-Aug;47(4):332-6. doi: 10.1053/j.jfas.2008.03.004. Epub 2008 May 12.
5
Case of nuchal fibroma.颈部纤维瘤病例。
J Dermatol. 2007 Jul;34(7):498-500. doi: 10.1111/j.1346-8138.2007.00320.x.
6
Nuchal fibroma presenting as two posterior neck masses.表现为颈部后方两个肿块的项部纤维瘤。
J Dermatol. 2007 Apr;34(4):262-3. doi: 10.1111/j.1346-8138.2007.00265.x.
7
A Japanese case of nuchal-type fibroma.一例日本的项部纤维瘤病例。
J Dermatol. 2005 Nov;32(11):931-2. doi: 10.1111/j.1346-8138.2005.tb00876.x.
8
Gardner-associated fibromas (GAF) in young patients: a distinct fibrous lesion that identifies unsuspected Gardner syndrome and risk for fibromatosis.年轻患者的加德纳相关纤维瘤(GAF):一种独特的纤维性病变,提示未被怀疑的加德纳综合征及纤维瘤病风险。
Am J Surg Pathol. 2001 May;25(5):645-51. doi: 10.1097/00000478-200105000-00012.
9
Nuchal fibroma should be recognized as a new extracolonic manifestation of Gardner-variant familial adenomatous polyposis.
Aust N Z J Surg. 2000 Nov;70(11):824-6. doi: 10.1046/j.1440-1622.2000.01958.x.
10
Nuchal-type fibroma in two related patients with Gardner's syndrome.两名患有加德纳综合征的相关患者的项部纤维瘤
Am J Surg Pathol. 2000 Nov;24(11):1563-7. doi: 10.1097/00000478-200011000-00015.