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YAP1-TFE3上皮样血管内皮瘤:一例无血管形成病例及一种新的转录变体

YAP1-TFE3 epithelioid hemangioendothelioma: a case without vasoformation and a new transcript variant.

作者信息

Puls Florian, Niblett Angela, Clarke Jade, Kindblom Lars-Gunnar, McCulloch Tom

机构信息

Department of Musculoskeletal Pathology, Royal Orthopaedic Hospital NHS Foundation Trust, Birmingham, UK,

出版信息

Virchows Arch. 2015 Apr;466(4):473-8. doi: 10.1007/s00428-015-1730-y. Epub 2015 Feb 14.

Abstract

Epithelioid hemangioendothelioma is a rare vascular tumor of borderline malignancy characterized by recurrent WWTR1-CAMTA1 gene fusions in approximately 90 % of cases. In addition, a recurrent YAP1-TFE3 gene fusion has been identified in WWTR1-CAMTA1 negative epithelioid hemangioendotheliomas. This subset has been reported as having a distinct morphology with more obvious vasoformation, voluminous eosinophilic cytoplasm, and TFE3 positivity on immunohistochemistry. We report a case of a YAP1-TFE3 translocated epithelioid hemangioendothelioma arising in a groin lymph node in a 29-year-old male. Plump spindle cell morphology and absence of vasoformation made correct diagnosis particularly difficult. Immunohistochemistry showed nuclear positivity for both ERG and TFE3, fluorescence in situ hybridization showed break apart for TFE3 and RT-PCR identified a YAP1 exon1 to TFE3 exon 6 transcript, a previously unreported fusion variant. Awareness of this solid morphology and variant fusion will aid in identification of future cases of this rare vascular tumor.

摘要

上皮样血管内皮瘤是一种罕见的交界性恶性血管肿瘤,约90%的病例具有复发性WWTR1-CAMTA1基因融合。此外,在WWTR1-CAMTA1阴性的上皮样血管内皮瘤中已鉴定出复发性YAP1-TFE3基因融合。据报道,该亚组具有独特的形态,血管形成更明显,嗜酸性细胞质丰富,免疫组化显示TFE3阳性。我们报告一例29岁男性腹股沟淋巴结发生的YAP1-TFE3易位的上皮样血管内皮瘤。丰满的梭形细胞形态和无血管形成使得正确诊断尤为困难。免疫组化显示ERG和TFE3均呈核阳性,荧光原位杂交显示TFE3分离,逆转录聚合酶链反应鉴定出YAP1外显子1至TFE3外显子6转录本,这是一种以前未报道的融合变体。认识到这种实体形态和变异融合将有助于识别未来这种罕见血管肿瘤的病例。

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