孕期原发性卵巢间叶性软骨肉瘤1例罕见病例。

A rare case of primary ovarian mesenchymal chondrosarcoma in pregnancy.

作者信息

Azizi Sepideh, Ghotbi Elena, Nassiri Setare

机构信息

Shahid Akbarabadi Clinical Research Development Unit (ShACRDU), Iran University of Medical Sciences (IUMS), Tehran, Iran.

Preventative Gynecology Research Center, Shahid Beheshti University of Medical Science, Tehran; 3Endometriosis Research Center, Iran University of Medical Science, Tehran, Iran.

出版信息

Clin Exp Reprod Med. 2022 Dec;49(4):285-288. doi: 10.5653/cerm.2022.05372. Epub 2022 Nov 28.

DOI:10.5653/cerm.2022.05372

PMID:36482503

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9732080/

Abstract

Mesenchymal chondrosarcoma is a rare tumor that is more common in young people; it is an uncommon type of chondrosarcoma with a poor prognosis. In two-thirds of cases, it affects the bone, especially the spine. However, parts of the body other than the skeletal system are occasionally involved. These rarer types have a worse prognosis, with a high likelihood of metastasis and death. Due to the possible misdiagnosis of mesenchymal chondrosarcoma, the integrated use of imaging, immunohistochemistry, and pathology can be helpful.

摘要

间叶性软骨肉瘤是一种罕见肿瘤，在年轻人中更为常见；它是软骨肉瘤的一种不常见类型，预后较差。在三分之二的病例中，它累及骨骼，尤其是脊柱。然而，骨骼系统以外的身体部位偶尔也会受累。这些较罕见的类型预后更差，转移和死亡的可能性很高。由于间叶性软骨肉瘤可能被误诊，综合运用影像学、免疫组织化学和病理学检查可能会有所帮助。