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Angiomatoid fibrous histiocytoma: staging and evaluation of response to therapy with F-18 FDG PET/CT.血管样纤维组织细胞瘤:F-18 FDG PET/CT分期及治疗反应评估
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2
Angiomatoid fibrous histiocytoma in a 25-year-old male.一名25岁男性的血管样纤维组织细胞瘤
Rare Tumors. 2010 Jun 30;2(2):e20. doi: 10.4081/rt.2010.e20.
3
Angiomatoid fibrous histiocytoma: magnetic resonance imaging appearance in 2 cases.血管样纤维组织细胞瘤:2例的磁共振成像表现
J Comput Assist Tomogr. 2010 Sep-Oct;34(5):791-4. doi: 10.1097/RCT.0b013e3181e39755.
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Imaging characteristics of angiomatoid fibrous histiocytoma of bone.骨血管外皮细胞瘤的影像学特征。
Skeletal Radiol. 2011 Feb;40(2):233-7. doi: 10.1007/s00256-010-1023-0. Epub 2010 Aug 30.
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Paraspinal malignant ossifying fibromyxoid tumor with spinal involvement.脊柱旁恶性骨化性纤维黏液样肿瘤伴脊柱累及。
J Clin Neurosci. 2010 Dec;17(12):1592-4. doi: 10.1016/j.jocn.2010.04.022.
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MFH classification: differentiating undifferentiated pleomorphic sarcoma in the 21st Century.黏液纤维肉瘤分类:21世纪未分化多形性肉瘤的鉴别
Expert Rev Anticancer Ther. 2009 Aug;9(8):1135-44. doi: 10.1586/era.09.76.
7
Angiomatoid fibrous histiocytoma: a review with recent genetic findings.血管样纤维组织细胞瘤:近期遗传学研究结果综述
Arch Pathol Lab Med. 2008 Feb;132(2):273-7. doi: 10.5858/2008-132-273-AFHARW.
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EWSR1-CREB1 is the predominant gene fusion in angiomatoid fibrous histiocytoma.EWSR1-CREB1是血管样纤维组织细胞瘤中主要的基因融合。
Genes Chromosomes Cancer. 2007 Dec;46(12):1051-60. doi: 10.1002/gcc.20491.
9
The evolving classification of soft tissue tumours: an update based on the new WHO classification.软组织肿瘤的分类进展:基于世界卫生组织新分类的更新
Histopathology. 2006 Jan;48(1):3-12. doi: 10.1111/j.1365-2559.2005.02284.x.
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MRI of angiomatoid fibrous histiocytoma.血管样纤维组织细胞瘤的磁共振成像
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血管样纤维组织细胞瘤:一例报告并文献复习

Angiomatoid fibrous histiocytoma: a case report and review of the literature.

作者信息

Bauer Adam, Jackson Bradley, Marner Erin, Gilbertson-Dahdal Dorothy

机构信息

Department of Radiology, University of Arizona Health Sciences Center, Tucson, AZ, USA.

出版信息

J Radiol Case Rep. 2012 Nov;6(11):8-15. doi: 10.3941/jrcr.v6i11.932. Epub 2012 Nov 1.

DOI:10.3941/jrcr.v6i11.932
PMID:23372863
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3558265/
Abstract

Angiomatoid fibrous histiocytoma (AFH) is a rare soft tissue tumor most commonly occurring in children, adolescents, and young adults. Clinically and radiographically the lesion is easily confused with a hematoma, soft tissue hemangioma, or malignant fibrous histiocytoma. While the lesion is rare, due to the potential for local recurrence and metastasis, it is imperative to consider this lesion in the differential diagnosis of a soft tissue mass in a child or adolescent. Here, we present the clinical, radiologic, and pathologic findings of a case of AFH.

摘要

血管样纤维组织细胞瘤(AFH)是一种罕见的软组织肿瘤,最常发生于儿童、青少年和年轻成年人。在临床和影像学上,该病变容易与血肿、软组织血管瘤或恶性纤维组织细胞瘤相混淆。虽然该病变罕见,但由于存在局部复发和转移的可能性,在儿童或青少年软组织肿块的鉴别诊断中必须考虑到这种病变。在此,我们报告一例AFH的临床、放射学和病理学表现。