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原发脾脏软组织肺泡状肉瘤 1 例报告并文献复习——重点介绍 TFE3 相关肿瘤谱。

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.

机构信息

Department of Pathology, Rouen University Hospital, Rouen, France.

Department of Hematology, Centre Henri Becquerel, Rouen, France.

出版信息

Diagn Pathol. 2024 Apr 20;19(1):62. doi: 10.1186/s13000-024-01483-4.

Abstract

BACKGROUND

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.

CASE PRESENTATION

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.

CONCLUSION

We described the first case of primary splenic alveolar soft part sarcoma, which questions once again the cell of origin of this rare tumour.

摘要

背景

腺泡状软组织肉瘤是一种罕见的软组织肿瘤,主要位于四肢的肌肉或深部软组织中。在极少数情况下,这种肿瘤会在腹部或骨盆的深部组织中发展。

病例介绍

在本病例报告中,我们描述了一例 46 岁男性原发性脾腺泡状软组织肉瘤病例。肿瘤表现出典型的形态学腺泡状外观,以及免疫组织化学 TFE3 核染色特征。分子生物学检测到 ASPSCR1 外显子 7::TFE3 外显子 6 融合转录本和 FISH 中 TFE3 重排证实了诊断。

结论

我们描述了首例原发性脾腺泡状软组织肉瘤病例,这再次质疑了这种罕见肿瘤的起源细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b849/11031972/c82cf342d4e5/13000_2024_1483_Figb_HTML.jpg

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