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病例报告:孕期外阴低度肌成纤维细胞肉瘤首例。

Case Report: First case of low-grade myofibroblastic sarcoma of the vulva during pregnancy.

作者信息

Zhu San, Luo Yan, Bian Ce, Zhang Yaoyao, Yang Lingyun

机构信息

Department of Gynecology and Obstetrics, West China Second University Hospital, Sichuan University, Chengdu, China.

West China School of Medicine, Sichuan University, Chengdu, China.

出版信息

Front Oncol. 2025 Jun 10;15:1577068. doi: 10.3389/fonc.2025.1577068. eCollection 2025.

Abstract

Low-grade myofibroblastic sarcoma (LGMFS) of the vulva is exceptionally rare, with only two prior cases reported. We present the third documented case globally and the first occurring during pregnancy, highlighting diagnostic and therapeutic challenges in this unique clinical scenario. A 34-year-old woman presented with a recurrent vulvar mass initially misdiagnosed as angiomyofibroblastoma. The lesion reappeared asymptomatically during pregnancy and was conservatively managed with ultrasound surveillance, followed by term cesarean delivery to mitigate perineal trauma risks. Postpartum evaluation revealed a 3.7 cm T2-hyperintense nodule on MRI. Although intraoperative frozen sections suggested benign margins, definitive histopathology and molecular studies (CD34+/SMA+; FISH-negative for COL1A1::PDGFB fusion and MDM2 amplification) confirmed LGMFS. Radical vulvectomy with 2 cm margins achieved disease-free survival at 17 months without adjuvant therapies. This case underscores that LGMFS may recur silently during pregnancy, necessitating rigorous histopathological re-evaluation of prior benign diagnoses. Multidisciplinary coordination enabled safe deferral of definitive surgery until postpartum without compromising outcomes, while radical excision alone proved curative, reflecting the tumor's indolent biology. Our findings establish the first pragmatic framework for managing vulvar LGMFS in pregnancy, emphasizing tailored surgical planning over routine adjuvant interventions.

摘要

外阴低度恶性肌成纤维细胞肉瘤(LGMFS)极为罕见,此前仅报道过两例。我们报告了全球第三例有记录的病例,也是首例发生在孕期的病例,突出了这种独特临床情况下的诊断和治疗挑战。一名34岁女性出现复发性外阴肿物,最初被误诊为血管肌成纤维细胞瘤。该病变在孕期无症状复发,通过超声监测进行保守处理,随后足月剖宫产以降低会阴创伤风险。产后评估显示磁共振成像(MRI)上有一个3.7厘米的T2高信号结节。尽管术中冰冻切片提示切缘良性,但最终的组织病理学和分子研究(CD34+/平滑肌肌动蛋白+;FISH检测COL1A1::PDGFB融合和MDM2扩增均为阴性)确诊为LGMFS。切缘2厘米的根治性外阴切除术实现了17个月无病生存,未进行辅助治疗。该病例强调LGMFS可能在孕期悄然复发,需要对先前的良性诊断进行严格的组织病理学重新评估。多学科协作使得能够安全地将确定性手术推迟到产后而不影响治疗效果,同时仅根治性切除就证明具有治愈性,反映了肿瘤的惰性生物学行为。我们的研究结果建立了首个针对孕期外阴LGMFS管理的实用框架,强调定制化手术规划而非常规辅助干预。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ebc/12185280/bac3b1e4070f/fonc-15-1577068-g001.jpg

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