舌头上的单发纤维瘤

Q4 Medicine Autopsy and Case Reports Pub Date : 2022-11-17 eCollection Date: 2022-01-01 DOI:10.4322/acr.2021.405
Juliana Mota Siqueira, Daniele Heguedusch, Emília Maria Gomes Aguiar, Anaeliza Figueiredo Dos Santos, Fabio Abreu Alves, Fabio Daumas Nunes
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摘要

孤立性纤维瘤(SFT)是一种良性间充质肿瘤,最初出现在胸膜,但在口腔中却很少见。在此,我们报告了一例 28 岁男性患者的病例,他的舌头前部有一个缓慢生长的无症状肿块。口腔内检查发现,肿块呈环状,由正常粘膜覆盖,呈纤维状。由于没有特异性临床发现,最初的诊断假设包括良性粘膜下肿瘤,如雷母细胞瘤、神经纤维瘤、SFT 等。患者接受了切除活检。显微镜下,肿瘤被厚厚的纤维囊包围;低细胞区和高细胞区呈星状排列,基质由胶原和丰富的血管形成。肿瘤细胞显示 CD34 和 STAT-6 免疫阳性,无 CD99、AML、S-100 和 Ki-67 表达。根据这些结果,确定了 SFT 的诊断。24 个月后,患者没有任何症状,也没有复发的迹象。虽然口腔受累很少见,但 SFT 应被纳入口腔黏膜下病变的鉴别诊断中。
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Solitary fibrous tumor of the tongue.

Solitary fibrous tumor (SFT) is a benign mesenchymal neoplasm originally described in pleura with a rare presentation in the oral cavity. Herein, we report a case of a 28-year-old male patient who presented an asymptomatic slow-growing mass in the anterior part of the tongue. Intraoral examination revealed a well-circumscribed mass covered by normal mucosa with a fibrous consistency. Due to non-specific clinical findings, the initial diagnostic hypotheses include benign submucosal neoplasms such as leiomyoma, neurofibroma, SFT, and others. An excisional biopsy was performed. Microscopically, the tumor was surrounded by a thick fibrous capsule; hypo and hypercellular areas were arranged in a storiform pattern with a stroma formed by collagen and abundant vascularization. Tumor cells showed immunopositivity for CD34 and STAT-6 and no expression of CD99, AML, S-100, and Ki-67. According to these findings, the diagnosis of SFT was established. After 24 months, the patient is asymptomatic and has no evidence of recurrence. Although oral involvement is rare, SFT should be included in the differential diagnosis of oral submucosal lesions.

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来源期刊
Autopsy and Case Reports
Autopsy and Case Reports Medicine-Internal Medicine
CiteScore
1.20
自引率
0.00%
发文量
60
审稿时长
9 weeks
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