A novel CDKN1A-JAZF1 gene fusion in low-grade endometrial stromal sarcoma arising from endometriosis in abdominal wall cesarean section scar: A case report and literature review

被引:5
|
作者
Zhu, Tian-Hong [1 ]
Zhang, Fu-Bin [1 ]
Yan, Hui [1 ]
Yu, Wen-Ying [2 ]
Chen, Mei [3 ]
Guan, Yu-Tao [1 ]
机构
[1] Ningbo First Hosp, Dept Obstet & Gynecol, Ningbo, Zhejiang, Peoples R China
[2] Ningbo Diagnost Pathol Ctr, Ningbo, Zhejiang, Peoples R China
[3] Ningbo First Hosp, Dept Ultrasonog, Ningbo, Zhejiang, Peoples R China
来源
关键词
Endometrial stromal sarcoma; Endometriosis; Gene fusion; CD10; CDKN1A/JAZF1; JAZF1; REARRANGEMENT; TUMOR; P21; P53;
D O I
10.1016/j.tjog.2022.04.010
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: We report a low-grade endometrial stromal sarcoma (ESS) with a novel CDKN1A-JAZF1 fusion gene arising from abdominal wall endometrioma. Case report: A 40-year-old woman presented with a 5.5-cm abdominal wall mass juxtaposed to the postoperative scar of two cesarean sections. Histologically, the tumor exhibited obvious tongue-like protrusions into the surrounding tissue, showed spindle cells with multinodular growth pattern that occasionally rotate around small arteries. Immunohistochemically, the tumor cells were positive for CD10, estrogen receptor (ER), progesterone receptor (PR), negatively stained for smooth muscle actin (SMA), CD117, CyclinD1. In addition, a previously undescribed gene fusion between CDNK1A 50 end of exon 1(NM_000389.5) and JAZF1 30 end of exon 5 (NM_175,061,3) was reported in this case. Conclusion: This report of ESS suggesting that rapidly growing abdominal wall masses without menstruation-related should be promptly evaluated and treated aggressively. In addition, we have expanded the molecular landscape of low-grade ESS. (c) 2022 Taiwan Association of Obstetrics & Gynecology. Publishing services by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:1082 / 1085
页数:4
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