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41例外周骨化性纤维瘤的临床病理特征

Clinicopathological features of peripheral ossifying fibroma in a series of 41 patients.

作者信息

Lázare H, Peteiro A, Pérez Sayáns M, Gándara-Vila P, Caneiro J, García-García A, Antón I, Gándara-Rey J M, Suárez-Peñaranda J M

机构信息

Department of Pathology, Clinical University Hospital, Santiago de Compostela, Spain.

Department of Pathology, Hospital POVISA, Vigo, Spain.

出版信息

Br J Oral Maxillofac Surg. 2019 Dec;57(10):1081-1085. doi: 10.1016/j.bjoms.2019.09.020. Epub 2019 Oct 8.

Abstract

Peripheral ossifying fibromas are benign mesenchymal lesions that usually arise in the anterior maxilla of young female patients. Histologically they consist of spindle cell proliferation with focal mineralisation. We reviewed 48 specimens from 41 patients and recorded the clinical data, sex, and age of the patients, site and size of the lesions, treatment, and postoperative outcome. Histologically the presence of mature, woven bone, cementum, and calcifications were evaluated and evaluated immunohistochemically. Lesions were more frequent in female patients in the third and fourth decade, and were usually in the lower maxilla and smaller than 2cm. All lesions were conservatively excised, and they relapsed in eight patients. Histopathologically, the lesions were poorly circumscribed, moderately cellular proliferations, with no discernible architectural pattern. All tumours showed some degree of mineralisation, the presence of immature bone being the most common. Immunohistochemical examination showed staining of tumoural cells for smooth muscle actin and CD68. Lesions tended to occur more commonly in female patients, but one decade later than usually reported. We found a higher recurrence rate in lesions that contained cementum-like material but without bone formation, suggesting a lack of maturation in this group. Immunohistochemical results were consistent with myofibroblastic differentiation but they added no information about the behaviour of the lesions.

摘要

外周骨化性纤维瘤是一种良性间叶性病变,通常发生于年轻女性患者的上颌前部。组织学上,它们由伴有局灶性矿化的梭形细胞增殖构成。我们回顾了41例患者的48份标本,并记录了患者的临床资料、性别、年龄、病变部位和大小、治疗方法及术后结果。组织学上,评估了成熟编织骨、牙骨质和钙化的存在情况,并进行了免疫组化评估。病变在第三和第四个十年的女性患者中更为常见,通常位于下颌骨下部,且小于2厘米。所有病变均采用保守切除,8例患者复发。组织病理学上,病变边界不清,为中度细胞增殖,无明显结构模式。所有肿瘤均有一定程度的矿化,最常见的是存在不成熟骨。免疫组化检查显示肿瘤细胞平滑肌肌动蛋白和CD68染色阳性。病变在女性患者中往往更常见,但比通常报道的时间晚十年。我们发现,含有类牙骨质物质但无骨形成的病变复发率较高,提示该组病变缺乏成熟度。免疫组化结果与肌成纤维细胞分化一致,但未提供有关病变行为的更多信息。

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