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头颈部软组织骨化性纤维黏液样肿瘤:病例报告及文献复习

Ossifying Fibromyxoid tumor of soft parts in head and neck: case report and literature review.

作者信息

Velasco Ignacio A, Zhang Ran, Li Tiejun, Wang Diancan

机构信息

Department of Oral and Maxillofacial Surgery, Peking University School and Hospital of Stomatology, 22 South Zhongguancun Avenue, Beijing, 100081, People's Republic of China.

Department of Oral Pathology, Peking University School and Hospital of Stomatology, Beijing, People's Republic of China.

出版信息

Diagn Pathol. 2018 Mar 27;13(1):21. doi: 10.1186/s13000-018-0699-7.

Abstract

BACKGROUND

Ossifying fibromyxoid tumor of soft parts (OFMT), is a rare but morphologically distinctive neoplasm of uncertain histogenesis that most frequently affects middle-aged male adults. Clinically, it usually presents as a slowly enlarging, small, circumscribed mass, which in most cases is painless. OFMT is most frequently found within the subcutaneous tissues of extremities or trunk, and rarely in the oral/head and neck region. We present an unusual case of this tumor in the submandibular region, and, based on the current medical literatures this is probably the first case described in this anatomical location.

CASE PRESENTATION

A 32-year-old male presented to our outpatient clinic with a right submandibular mass with 1-year of evolution. Excisional biopsy showed that it was characterized by ossification along the periphery of the lesion. The neoplastic cells were spindle-like with scant eosinophilic cytoplasm. These cells were arranged with uniform cell-to-cell space in a fibromyxoid stroma. Small and large clusters of calcifications were present within the tumor. Immunohistochemically, the case showed positive staining of S-100 protein, vimentin, nestin, calponin, SMA, GFAF, desmin, INI-1, caldesmon, and CD34. It also showed negative staining of CK, CK7, CK8/18, NF, and EMA. About 2% of neoplastic cells showed positive staining of Ki67. Based on these features, the final pathological diagnosis was OFMT.

CONCLUSIONS

It is hoped that a greater understanding of OFMT in the head and neck region will avoid potential misdiagnosis, and contribute to determining the correct management, which appears to be complete surgical excision with close follow-up for recurrence surveillance.

摘要

背景

软组织骨化性纤维黏液样肿瘤(OFMT)是一种罕见但形态独特的肿瘤,其组织发生尚不明确,最常发生于中年男性。临床上,它通常表现为缓慢增大的、小的、边界清楚的肿块,多数情况下无痛。OFMT最常见于四肢或躯干的皮下组织,很少见于口腔/头颈部区域。我们报告一例发生于下颌下区的该肿瘤罕见病例,根据现有医学文献,这可能是首例报道于该解剖部位的病例。

病例报告

一名32岁男性因右侧下颌下肿物就诊于我院门诊,病程1年。切除活检显示其特征为病变周边骨化。肿瘤细胞呈梭形,嗜酸性胞质稀少。这些细胞在纤维黏液样基质中以均匀的细胞间距排列。肿瘤内可见大小不等的钙化灶。免疫组化显示,该病例S-100蛋白、波形蛋白、巢蛋白、钙调蛋白、平滑肌肌动蛋白、胶质纤维酸性蛋白、结蛋白、INI-1、钙结合蛋白和CD34呈阳性染色。细胞角蛋白、细胞角蛋白7、细胞角蛋白8/18、神经丝蛋白和上皮膜抗原呈阴性染色。约2%的肿瘤细胞Ki67呈阳性染色。基于这些特征,最终病理诊断为OFMT。

结论

希望对头颈部OFMT有更深入的了解,以避免潜在的误诊,并有助于确定正确的治疗方案,似乎是完整手术切除并密切随访以监测复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1241/5870216/027652796d1c/13000_2018_699_Fig1_HTML.jpg

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