Persistent Müllerian Duct Syndrome and Concurrent Pre-Germ Cell Neoplasia In Situ.

IF 1.3
Gabriel L Carreno-Galeano, Cynthia Fata, Lisal Folsom, Laura Cornwell
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Abstract

Persistent Müllerian duct syndrome (PMDS) is a rare disorder of sex development in 46,XY individuals, characterized by the presence of Müllerian duct structures and typically associated with cryptorchidism and an elevated risk of testicular malignancy. Germ cell neoplasia in situ (GCNIS) is a known precursor to testicular germ cell tumors, but the earlier stage of pre-GCNIS remains poorly characterized, particularly in the context of PMDS. We report the first known case of pre-GCNIS identified in a patient with PMDS. A male infant presented with a non-palpable right testis and was found to have intra-abdominal gonads with Müllerian remnants. Histopathology revealed centrally located gonocytes with OCT3/4 expression but without the morphological features of GCNIS, consistent with pre-GCNIS. Management included right orchiectomy and left orchiopexy. This case highlights the underrecognized early stages of germ cell dysregulation in PMDS and raises important considerations about the timing of gonadectomy, fertility preservation, and long-term surveillance. Further research is needed to clarify the malignant potential of pre-GCNIS in DSD populations and to inform individualized, risk-based management strategies.

持续性勒氏管综合征和并发生殖前细胞原位瘤。
持续性勒氏管综合征(PMDS)是一种罕见的性发育障碍,发生于46,xy个体,其特征是存在勒氏管结构,通常与隐睾和睾丸恶性肿瘤风险升高有关。生殖细胞原位瘤(GCNIS)是已知的睾丸生殖细胞肿瘤的前体,但GCNIS前期的早期阶段仍然缺乏特征,特别是在PMDS的背景下。我们报告第一个已知的病例前gcnis确定在患者与PMDS。一个男婴提出了一个不可触及的右睾丸,并被发现有腹内性腺与勒氏残余。组织病理学显示中心位置的gonocytes表达OCT3/4,但没有GCNIS的形态学特征,与GCNIS前一致。治疗包括右睾丸切除术和左睾丸切除术。本病例强调了经前综合症中未被认识到的生殖细胞失调的早期阶段,并提出了关于性腺切除术、生育能力保存和长期监测的重要考虑。需要进一步的研究来阐明DSD人群中gcnis前病变的恶性潜力,并为个性化的、基于风险的管理策略提供信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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