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舌根部平滑肌瘤性错构瘤

[Leiomyomatous hamartoma at base of tongue].

作者信息

Hahn Christoffer Holst, Munch-Petersen Helga Richert

机构信息

Naestved Sygehus, Øre-naese-halsafdeling, og Gentofte/Herlev Hospitaler, Patologisk Afdeling, Denmark.

出版信息

Ugeskr Laeger. 2010 Mar 1;172(9):710-1.

PMID:20199749
Abstract

We report a case of a leiomyomatous hamartoma located in the midline of the base of the tongue. The two-year-old girl had an asymptomatic pedunculated tubular tumour measuring 1.6 x 1.3 x 1.1 cms. The lesion was surgically excised, and histopathological examination disclosed a non-neoplastic mass composed of irregular arranged bundles of smooth muscle cells embedded in a fibrovascular stroma. The diagnosis was confirmed by immunohistochemistry with positivity for smooth muscle actin and desmin. Until now, only 19 cases have been reported in English-language literature.

摘要

我们报告一例位于舌根部中线的平滑肌瘤性错构瘤。该两岁女童有一个无症状的带蒂管状肿瘤,大小为1.6×1.3×1.1厘米。病变经手术切除,组织病理学检查显示为非肿瘤性肿块,由嵌入纤维血管基质中的不规则排列的平滑肌细胞束组成。通过免疫组织化学检测平滑肌肌动蛋白和结蛋白呈阳性,确诊得以证实。迄今为止,英文文献中仅报道了19例。

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1
[Leiomyomatous hamartoma at base of tongue].舌根部平滑肌瘤性错构瘤
Ugeskr Laeger. 2010 Mar 1;172(9):710-1.
2
Leiomyomatous hamartoma: report of two cases and review of the literature.
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Leiomyomatous hamartoma presenting as a congenital epulis.表现为先天性龈瘤的平滑肌瘤性错构瘤。
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Leiomyomatous hamartoma of the midline maxillary gingival presenting as a congenital epulis: a case report with an immunohistochemical study.中线上颌牙龈的平滑肌瘤性错构瘤表现为先天性龈瘤:一例病例报告并免疫组织化学研究。
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引用本文的文献

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A systematic review of the clinicopathological characteristics of oral leiomyomatous hamartoma.口腔平滑肌瘤样错构瘤临床病理特征的系统评价
World J Surg Oncol. 2024 Dec 5;22(1):326. doi: 10.1186/s12957-024-03607-y.
2
Lingual leiomyomatous hamartoma with bifid tip and ankyloglossia in a patient without oral-facial-digital syndrome: a case report and literature review.患者无口腔面指综合征,表现为舌尖分叉和舌系带过短的舌部平滑肌瘤性错构瘤:病例报告及文献复习。
World J Surg Oncol. 2013 Sep 16;11:230. doi: 10.1186/1477-7819-11-230.