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2
FOSB is a Useful Diagnostic Marker for Pseudomyogenic Hemangioendothelioma.FOSB是假性肌源性血管内皮瘤的一种有用诊断标志物。
Am J Surg Pathol. 2017 May;41(5):596-606. doi: 10.1097/PAS.0000000000000795.
3
Pseudomyogenic Hemangioendothelioma: A Vascular Tumor Previously Undescribed in the Oral Cavity.假肌源性血管内皮瘤:一种口腔内此前未被描述过的血管肿瘤。
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4
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Histopathology. 2015 Dec;67(6):827-35. doi: 10.1111/his.12713. Epub 2015 May 22.
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Cancer. 2014 Jun 15;120(12):1763-74. doi: 10.1002/cncr.28657. Epub 2014 Mar 19.
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Epithelioid rhabdomyosarcoma: a clinicopathologic and molecular study.上皮样横纹肌肉瘤:临床病理和分子研究。
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A novel SERPINE1-FOSB fusion gene results in transcriptional up-regulation of FOSB in pseudomyogenic haemangioendothelioma.一种新型 SERPINE1-FOSB 融合基因导致假性肌源性血管内皮瘤中 FOSB 的转录上调。
J Pathol. 2014 Apr;232(5):534-40. doi: 10.1002/path.4322. Epub 2014 Jan 29.
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Pseudomyogenic (epithelioid sarcoma-like) hemangioendothelioma: characterization of five cases.假肌源性(上皮样肉瘤样)血管内皮瘤:五例病例特征。
Skeletal Radiol. 2013 Jul;42(7):947-57. doi: 10.1007/s00256-013-1577-8. Epub 2013 Feb 5.
9
Translocation t(7;19)(q22;q13)−a recurrent chromosome aberration in pseudomyogenic hemangioendothelioma?易位t(7;19)(q22;q13)——假肌源性血管内皮瘤中的一种复发性染色体畸变?
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10
Pseudomyogenic hemangioendothelioma: a distinctive, often multicentric tumor with indolent behavior.假肌源性血管内皮瘤:一种具有惰性行为的独特、常为多中心肿瘤。
Am J Surg Pathol. 2011 Feb;35(2):190-201. doi: 10.1097/PAS.0b013e3181ff0901.

口腔假肌源性血管内皮瘤:病例报告及文献复习。

Oral Pseudomyogenic Hemangioendothelioma: Case Report and Review of the Literature.

机构信息

Division of Oral and Maxillofacial Pathology, Columbia University Medical Center, 630 West 168th Street, PH15-1562W, New York, NY, 10032, USA.

Department of Oral and Maxillofacial Surgery, Columbia University Medical Center, New York, NY, USA.

出版信息

Head Neck Pathol. 2020 Dec;14(4):1134-1138. doi: 10.1007/s12105-020-01137-z. Epub 2020 Feb 3.

DOI:10.1007/s12105-020-01137-z
PMID:32016785
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7669923/
Abstract

Pseduomyogenic hemangioendothelioma (PMH) is a vascular neoplasm of intermediate biological potential first described by Hornick and Fletcher (Am J Surg Pathol 35:190-201, 2011). Despite its initial categorization as a malignant entity, PMH often demonstrates an indolent behavior profile, and thus was classified as a rarely metastasizing endothelial neoplasm in the 2013 WHO Classification of Tumors of Soft Tissue and Bone. It is a tumor primarily of skin and soft tissue, with most reported cases involving the trunk or extremities. To date, only one case of PMH involving the oral cavity has been reported. Herein, we present a case of PMH involving the mandibular gingiva and vestibule of a 33-year-old female and discuss the salient features of this entity.

摘要

假性肌源性血管内皮瘤(PMH)是一种中等生物学潜能的血管肿瘤,最初由 Hornick 和 Fletcher 描述(Am J Surg Pathol 35:190-201, 2011)。尽管最初被归类为恶性实体瘤,但 PMH 通常表现出惰性的行为特征,因此在 2013 年软组织和骨骼肿瘤 WHO 分类中被归类为罕见转移的内皮肿瘤。它主要是皮肤和软组织的肿瘤,大多数报道的病例涉及躯干或四肢。迄今为止,仅有一例口腔 PMH 的报道。在此,我们报告一例发生于 33 岁女性下颌牙龈和口腔前庭的 PMH,并讨论该肿瘤的特征。