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本文引用的文献

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EWSR1-POU5F1 fusion in soft tissue myoepithelial tumors. A molecular analysis of sixty-six cases, including soft tissue, bone, and visceral lesions, showing common involvement of the EWSR1 gene.EWSR1-POU5F1 融合基因在软组织肌上皮肿瘤中的表达。对 66 例软组织、骨和内脏病变的分子分析,显示 EWSR1 基因的常见累及。
Genes Chromosomes Cancer. 2010 Dec;49(12):1114-24. doi: 10.1002/gcc.20819.
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Chondroid syringoma. Mixed tumor of skin, salivary gland type.软骨样汗腺腺瘤。皮肤混合瘤,涎腺型。
Arch Dermatol. 1961 Nov;84:835-47. doi: 10.1001/archderm.1961.01580170129018.
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Myoepithelial tumors of soft tissue: a clinicopathologic and immunohistochemical study of 101 cases with evaluation of prognostic parameters.软组织肌上皮肿瘤:101例临床病理及免疫组化研究并评估预后参数
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Primary mixed tumor of bone.原发性骨混合瘤
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Recurrent malignant chondroid syringoma of the foot: a case report and review of the literature.足部复发性恶性软骨样汗腺腺瘤:一例报告并文献复习
Am J Clin Oncol. 2000 Jun;23(3):227-32. doi: 10.1097/00000421-200006000-00003.
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Intraosseous chondroid syringoma of the hallux.
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Chondroid syringoma (mixed tumour) of radius.桡骨的软骨样汗腺螺旋瘤(混合瘤)。
Indian J Cancer. 1981 Mar;18(1):81-3.
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Malignant chondroid syringoma--a rare cause of secondary bone tumour.恶性软骨样汗腺螺旋瘤——继发性骨肿瘤的罕见病因。
Clin Exp Dermatol. 1991 Jul;16(4):306-7. doi: 10.1111/j.1365-2230.1991.tb00384.x.

一名18岁男性的原发性骨混合性恶性肿瘤:一例影像学与病理对照报告

Primary mixed malignant tumor of bone in an 18-year-old male: Report of a case with radiologic-pathologic correlation.

作者信息

Courtier Jesse, Robbins Elizabeth, Soares Bruno, Horvai Andrew, Mackenzie John D

机构信息

Departments of Radiology and Biomedical Imaging, University of California San Francisco, Benioff Children's Hospital, United States.

Pediatric Hematology-Oncology, University of California San Francisco, Benioff Children's Hospital, United States.

出版信息

J Bone Oncol. 2012 Dec 1;1(3):101-5. doi: 10.1016/j.jbo.2012.10.002. eCollection 2012 Dec.

DOI:10.1016/j.jbo.2012.10.002
PMID:26909264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4723350/
Abstract

We report a case of primary malignant mixed tumor (MMT) of bone in an 18-year-old boy with X-ray, CT, MR, scintigraphic, FDG PET, and pathologic correlation. Primary MMT of bone is a highly aggressive tumor and presents both a diagnostic and clinical treatment challenge. This tumor is extremely rare and to the best of our knowledge, this is the first report of the diagnostic imaging findings for primary MMT arising from bone in a patient of this age group.

摘要

我们报告一例18岁男性原发性骨恶性混合瘤(MMT)病例,并结合X线、CT、MR、骨闪烁显像、FDG PET及病理结果进行分析。原发性骨MMT是一种侵袭性很强的肿瘤,在诊断和临床治疗方面均具有挑战性。该肿瘤极为罕见,据我们所知,这是该年龄组患者原发性骨MMT诊断性影像学表现的首例报告。