Uterine Myxoid Leiomyosarcoma with Stroma Chondroid Metaplasia: A Rare Case Report

被引:0
作者
Aslani, Fatemeh Sari [1 ]
Taheri, Negar [2 ]
Najib, Fatemehsadat [3 ]
Akbarzadeh-Jahromi, Mojgan [1 ]
机构
[1] Shiraz Univ Med Sci, Maternal Fetal Med Res Ctr, Pathol Dept, Shiraz, Iran
[2] Shiraz Univ Med Sci, Sch Med, Pathol Dept, Shiraz, Iran
[3] Shiraz Univ Med Sci, Infertil Res Ctr, Sch Med, Obstet & Gynaecol Dept, Shiraz, Iran
来源
GALEN MEDICAL JOURNAL | 2021年 / 10卷
关键词
Myxoid Leiomyosarcoma; Leiomyosarcoma; Metaplasia; Uterus; UTERUS; TUMORS; PATHOLOGY;
D O I
10.31661/gmj.v10i0.1817
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Uterine leiomyosarcoma is a rare gynecological disease. Myxoid leiomyosarcoma (mLMS) is an aggressive and very uncommon type of lciomyosarcoma, with few cases reported in English literature. Stromal metaplasia is rare in leiomyosarcoma. Here we present huge uterine myxoid leiomyosarcoma with stromal chondroid metaplasia. Case Presentation: A 48-year-old single woman with lower abdominal pain and increased abdominal circumference. The detected mass on imaging was diagnosed as uterine mLMS with stromal chondroid metaplasia in the histopathological examination after surgery. Conclusion: Myxoid leiomyosarcoma should be considered in uterine mass with extensive myxoid change, infiltrative border, low mitotic count, and mild atypia. Stromal chondroid metaplasia can be seen in the myxoid leiomvosarcoma.
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页数:6
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