Department of Pathology, West China Second University Hospital, Sichuan University, Chengdu, 610041, China.
Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Chengdu, 610041, China.
Diagn Pathol. 2024 Apr 3;19(1):56. doi: 10.1186/s13000-024-01477-2.
Müllerian adenosarcoma, a rare malignancy, presents diagnostic and therapeutic challenges. In this study, we conducted an analysis of the clinicopathological characteristics of 22 adenosarcomas, with a particular focus on screening for DICER1 hot mutations.
The cohort consisted of patients with adenosarcoma who were registered at the West China Second Hospital between the years 2020 and June 2022. Sanger sequencing was employed to screen for somatic Hotspot mutations in the RNase IIIb domain of DICER1 in the 22 adenosarcomas.
Only one patient exhibited a DICER1 mutation that was not a DICER1 Hotspot mutation. Among the 22 patients, all underwent total hysterectomy with bilateral salpingo-oophorectomy, and 14 out of these 22 patients received adjuvant treatment.
In summary, our study of 22 Müllerian adenosarcomas focused on the clinicopathological features and the presence of DICER1 Hotspot mutations. Although our findings did not reveal any DICER1 mutations in the studied samples, this negative result provides valuable information for the field by narrowing down the genetic landscape of adenosarcomas and highlighting the need for further research into alternative molecular pathways driving this malignancy.
苗勒管腺肉瘤是一种罕见的恶性肿瘤,在诊断和治疗方面均存在挑战。本研究对 22 例腺肉瘤的临床病理特征进行分析,重点筛查 DICER1 热点突变。
该队列纳入 2020 年至 2022 年 6 月在四川大学华西第二医院登记的腺肉瘤患者。采用 Sanger 测序法对 22 例腺肉瘤中 DICER1 的 RNase IIIb 结构域的体细胞热点突变进行筛查。
仅有 1 例患者存在非 DICER1 热点突变的 DICER1 突变。22 例患者均接受了全子宫切除术和双侧附件切除术,其中 14 例患者接受了辅助治疗。
总之,我们对 22 例苗勒管腺肉瘤的研究重点是临床病理特征和 DICER1 热点突变。虽然我们的研究结果在研究样本中未发现任何 DICER1 突变,但这一阴性结果通过缩小腺肉瘤的遗传图谱,强调了进一步研究驱动这种恶性肿瘤的替代分子途径的必要性,为该领域提供了有价值的信息。