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上颌窦黏液纤维肉瘤酷似结节性筋膜炎:罕见病例报告。

Maxillary Sinus Myxofibrosarcoma Mimicking Nodular Fasciitis: A Rare Case Report.

机构信息

Department of Oral and Maxillofacial Medicine, School of Dentistry, Yasuj University of Medical Sciences, Yasuj, Iran.

Department of Oral and Maxillofacial Radiology, School of Dentistry, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Head Neck Pathol. 2021 Dec;15(4):1372-1376. doi: 10.1007/s12105-021-01298-5. Epub 2021 Feb 5.

Abstract

Myxofibrosarcoma (MFS) is a fibroblastic soft tissue sarcoma that is extremely rare in the maxillofacial region. Due to its non-specific clinicoradiographic findings and challenging histopathological features, the diagnosis is difficult. Here, we present a case of MFS which was first diagnosed as nodular fasciitis. The initial examination of the incisional biopsy showed a benign-appearing proliferation of fibroblasts without features of malignancy. The patient returned with recurrence four months after surgical excision of the primary lesion. The second histologic study revealed a high-grade spindle cell sarcoma with myxoid features most compatible with MFS. Definitive diagnosis of MFS was confirmed by these histopathologic features and supportive immunohistochemical stains. Unfortunately, the patient died of disease 3 months later.

摘要

黏液纤维肉瘤(MFS)是一种极其罕见于颌面区域的纤维母细胞性软组织肉瘤。由于其非特异性的临床影像学表现和具有挑战性的组织病理学特征,诊断较为困难。在此,我们报告一例 MFS 病例,该病例最初被诊断为结节性筋膜炎。初次活检的检查显示良性表现的成纤维细胞增生,无恶性特征。患者在原发性病变切除术后 4 个月时因复发而返回。第二次组织学研究显示具有黏液样特征的高级别梭形细胞肉瘤,最符合 MFS 的表现。这些组织病理学特征和支持性免疫组织化学染色证实了 MFS 的明确诊断。不幸的是,患者在 3 个月后死于该疾病。

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Myxofibrosarcoma of unusual sites.罕见部位的黏液纤维肉瘤
J Cutan Pathol. 2018 Feb;45(2):104-110. doi: 10.1111/cup.13063. Epub 2017 Dec 5.
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Myxofibrosarcoma in Head and Neck: Case Report of Unusually Aggressive Presentation.头颈部黏液纤维肉瘤:侵袭性异常表现的病例报告
J Oral Maxillofac Surg. 2017 Dec;75(12):2709.e1-2709.e12. doi: 10.1016/j.joms.2017.08.015. Epub 2017 Aug 16.
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Nodular Fasciitis of the Orofacial Region: An Uncommon Differential.口面部结节性筋膜炎:一种罕见的鉴别诊断。
J Maxillofac Oral Surg. 2016 Jul;15(Suppl 2):328-31. doi: 10.1007/s12663-015-0864-4. Epub 2015 Dec 10.
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JAMA Otolaryngol Head Neck Surg. 2015 Jan;141(1):54-9. doi: 10.1001/jamaoto.2014.2797.
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Rare sarcoma presented as sinusitis.罕见肉瘤表现为鼻窦炎。
BMJ Case Rep. 2012 Aug 27;2012:bcr0220125863. doi: 10.1136/bcr-02-2012-5863.
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