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一名2岁儿童患多发性颈部纤维瘤,无加德纳综合征。

Multiple nuchal fibromas in a 2-year-old without Gardner syndrome.

作者信息

LeBlanc Keith G, Wenner Morgan, Davis Loretta S

机构信息

Division of Dermatology, Department of Medicine, Medical College of Georgia, Augusta, Georgia.

School of Medicine, Medical College of Georgia, Augusta, Georgia.

出版信息

Pediatr Dermatol. 2011 Nov-Dec;28(6):695-696. doi: 10.1111/j.1525-1470.2011.01415.x. Epub 2011 Sep 25.

DOI:10.1111/j.1525-1470.2011.01415.x
PMID:21950671
Abstract

Nuchal fibromas, uncommon benign soft tissue tumors typically arising along the posterior neck, are often associated with Gardner syndrome (GS). These tumors have rarely been reported in association with scleroderma or as secondary to trauma and diabetes. Nuchal fibromas not associated with GS have been described predominantly in men aged 30 to 50. We report a 2-year-old African American girl with multiple nuchal fibromas along the posterior aspect of her neck and upper back. Retinal examination showed no signs of congenital hypertrophy of the retinal pigment epithelium, and genetic testing for the adenomatous polyposis coli gene mutation seen in GS was negative.

摘要

颈部纤维瘤是一种罕见的良性软组织肿瘤,通常发生于后颈部,常与加德纳综合征(GS)相关。这些肿瘤很少被报道与硬皮病相关,或继发于创伤和糖尿病。与GS无关的颈部纤维瘤主要见于30至50岁的男性。我们报告一名2岁非裔美国女孩,其颈部后方和上背部有多个颈部纤维瘤。视网膜检查未发现视网膜色素上皮先天性肥大的迹象,对GS中所见的腺瘤性息肉病 coli基因突变进行的基因检测为阴性。

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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.
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Multiple nuchal-type fibromas on the scalp: a case report.
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Ann Dermatol. 2015 Apr;27(2):194-6. doi: 10.5021/ad.2015.27.2.194. Epub 2015 Mar 24.