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口腔血管内筋膜炎:一种罕见的颌面病变。

Oral intravascular fasciitis: a rare maxillofacial lesion.

机构信息

Oral and Maxillofacial Surgery, Tel-Aviv Sourasky Medical Center, Tel-Aviv, Israel.

出版信息

Oral Surg Oral Med Oral Pathol Oral Radiol. 2012 Aug;114(2):e40-4. doi: 10.1016/j.oooo.2012.03.027.

Abstract

Nodular fasciitis is a benign non-neoplastic myofibroblastic proliferation, involving the head in 7% to 20% of cases. Intravascular fasciitis (IVF) is a rare variant, with a unique intravascular growth pattern. Only 4 maxillofacial cases have been previously reported. We describe a 58-year-old woman with a rapidly growing, hard, mobile buccal submucosal swelling. CT scans identified a well-defined, 1.7-cm isodense lesion, located between the mental foramen and masseter muscle, which was excised under general anesthesia. A well-defined cellular nodular mass was composed of bland spindle cells, in a densely vascularized, focally myxoid matrix, involving an arterial lumen, and extending into adjacent tissues. Mitoses were rare. Immunohistochemistry was positive for smooth muscle actin, negative for keratins, S-100, epithelial membrane antigen, caldesmon, p53 and Alk. CD31 and CD34 were positive only in the vascular component, supporting the diagnosis of intravascular fasciitis.

摘要

结节性筋膜炎是一种良性非肿瘤性肌纤维母细胞增生,涉及头部的病例占 7%至 20%。血管内筋膜炎(IVF)是一种罕见的变异型,具有独特的血管内生长模式。以前仅报道了 4 例口腔颌面病例。我们描述了一位 58 岁女性,其颊黏膜下有一个快速生长的硬而可移动的肿块。CT 扫描发现一个界限清楚的 1.7cm 等密度病变,位于颏孔和咬肌之间,在全身麻醉下切除。一个界限清楚的细胞性结节状肿块由温和的梭形细胞组成,存在密集的血管化、局灶性黏液样基质,累及动脉管腔,并延伸至邻近组织。有丝分裂很少见。免疫组织化学染色平滑肌肌动蛋白阳性,角蛋白、S-100、上皮膜抗原、钙调蛋白、p53 和 Alk 阴性。CD31 和 CD34 仅在血管成分中阳性,支持血管内筋膜炎的诊断。

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