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口腔双侧胶原性纤维瘤:一例此前未报道的病例及文献综述。

Oral Bilateral Collagenous Fibroma: A previously unreported case and literature review.

作者信息

Vasconcelos Ana-Carolina, Gomes Ana-Paula, Tarquinio Sandra, Abduch-Rodrigues Eduardo, Mesquita Ricardo, Silva Karine

机构信息

PhD, Post Graduate Program in Dentistry, School of Dentistry, Federal University of Pelotas, Pelotas-RS, Brazil.

MSc, Residence Program in Oral and Maxillofacial Surgery and Traumatology, Federal University of Pelotas-RS, Brazil.

出版信息

J Clin Exp Dent. 2018 Jan 1;10(1):e96-e99. doi: 10.4317/jced.54123. eCollection 2018 Jan.

DOI:10.4317/jced.54123
PMID:29670724
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5899808/
Abstract

Collagenous fibroma, also known as desmoplastic fibroblastoma, is a rare benign slow growing tumor particularly uncommon in the oral cavity. The aim of this study was to analyze the clinical and histopathological features of an oral collagenous fibroma as well as to compare this data with those reported in an English-literature review. The thirteenth case of collagenous fibroma in the oral cavity and the first to present clinically as a bilateral mass was described. A 48-years-old female patient was referred to a School of Dentistry, complaining about an asymptomatic swelling on the hard palate, lasting around ten years. The intraoral examination revealed two well-defined mass, bilaterally in the hard palate. An excisional biopsy was performed. Microscopically, the connective tissue consisted of dense collagen bundles in which were seen scarcely distributed spindle-shaped to stellate fibroblastic cells. Blood vessels were few, as well as inflammatory cells. Immunohistochemical staining was positive for vimentin, α-smooth muscle actin and factor XIIIa and negative for S-100, CD68, CD34, HHF35, desmin and AE1/AE3. The patient remains disease-free 24 months after excision. In conclusion, oral collagenous fibroma should be included in the differential diagnosis of bilateral sessile nodules in the oral cavity. Connective tissue, mouth diseases, mouth neoplasms, oral diagnosis, oral pathology.

摘要

胶原纤维瘤,也称为促结缔组织增生性纤维母细胞瘤,是一种罕见的良性缓慢生长肿瘤,在口腔中尤为少见。本研究的目的是分析口腔胶原纤维瘤的临床和组织病理学特征,并将这些数据与英文文献综述中报道的数据进行比较。本文描述了口腔内第13例胶原纤维瘤,也是首例临床上表现为双侧肿块的病例。一名48岁女性患者因硬腭无症状肿胀约十年被转诊至一所牙科学院。口腔检查发现硬腭双侧有两个边界清晰的肿块。进行了切除活检。显微镜下,结缔组织由密集的胶原束组成,其中可见散在分布的梭形至星状成纤维细胞。血管很少,炎症细胞也很少。免疫组织化学染色波形蛋白、α-平滑肌肌动蛋白和因子XIIIa呈阳性,而S-100、CD68、CD34、HHF35、结蛋白和AE1/AE3呈阴性。患者切除术后24个月无疾病复发。总之,口腔胶原纤维瘤应纳入口腔双侧无蒂结节的鉴别诊断。结缔组织、口腔疾病、口腔肿瘤、口腔诊断、口腔病理学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56bd/5899808/1fe5ccddb413/jced-10-e96-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56bd/5899808/9f46e70d2c38/jced-10-e96-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56bd/5899808/261c46eb1a8c/jced-10-e96-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56bd/5899808/1fe5ccddb413/jced-10-e96-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56bd/5899808/9f46e70d2c38/jced-10-e96-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56bd/5899808/261c46eb1a8c/jced-10-e96-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56bd/5899808/1fe5ccddb413/jced-10-e96-g003.jpg

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Turk Patoloji Derg. 2018;34(3):247-250. doi: 10.5146/tjpath.2015.01355.
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Desmoplastic fibroblastoma (collagenous fibroma) of the oral cavity.口腔促结缔组织增生性纤维瘤(胶原性纤维瘤)
J Clin Exp Dent. 2016 Feb 1;8(1):e89-92. doi: 10.4317/jced.52605. eCollection 2016 Feb.
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Desmoplastic fibroblastoma (collagenous fibroma) in the oral cavity.
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A prevertebral desmoplastic fibroblastoma presenting with sleep-related breathing dysfunction.一例表现为睡眠相关呼吸功能障碍的椎前促结缔组织增生性纤维母细胞瘤
Clin Case Rep. 2021 Feb 10;9(3):1767-1770. doi: 10.1002/ccr3.3897. eCollection 2021 Mar.
口腔促结缔组织增生性纤维瘤(胶原纤维瘤)
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Collagenous fibroma (desmoplastic fibroblastoma) of the oral cavity.口腔胶原纤维瘤(促结缔组织增生性纤维母细胞瘤)
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Head Neck Pathol. 2011 Jun;5(2):175-9. doi: 10.1007/s12105-010-0239-6. Epub 2011 Jan 8.
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