一例不寻常的原发性脾脏软组织肺泡肉瘤:病例报告和文献综述,重点是 TFE3 相关肿瘤的范围

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
René Guérin, Anne-Lise Menard, Emilie Angot, Nicolas Piton, Pierre Vera, Lilian Schwarz, Jean-Christophe Sabourin, Marick Laé, Pierre-Alain Thiébaut
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引用次数: 0

摘要

肺泡软组织肉瘤是一种罕见的软组织肿瘤,多发于四肢肌肉或深层软组织。在极少数情况下,这种肿瘤也会发生在腹部或骨盆的深层组织中。在本病例报告中,我们描述了一名 46 岁男性的原发性脾肺泡软组织肉瘤病例。该肿瘤具有典型的肺泡形态和免疫组化特征,尤其是 TFE3 核染色。分子生物学检测到 ASPSCR1 外显子 7::TFE3 外显子 6 融合转录本,FISH 检测到 TFE3 重排,确诊该肿瘤。我们描述了第一例原发性脾脏肺泡软组织肉瘤,再次质疑了这种罕见肿瘤的起源细胞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An unusual case of primary splenic soft part alveolar sarcoma: case report and review of the literature with emphasis on the spectrum of TFE3-associated neoplasms
Alveolar soft part sarcoma is a rare tumour of soft tissues, mostly localized in muscles or deep soft tissues of the extremities. In rare occasions, this tumour develops in deep tissues of the abdomen or pelvis. In this case report, we described the case of a 46 year old man who developed a primary splenic alveolar soft part sarcoma. The tumour displayed typical morphological alveolar aspect, as well as immunohistochemical profile notably TFE3 nuclear staining. Detection of ASPSCR1 Exon 7::TFE3 Exon 6 fusion transcript in molecular biology and TFE3 rearrangement in FISH confirmed the diagnosis. We described the first case of primary splenic alveolar soft part sarcoma, which questions once again the cell of origin of this rare tumour.
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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