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XY 性发育障碍患者的恶性生殖细胞肿瘤及其前体细胞性腺病变:病例系列及文献复习。

Malignant Germ Cell Tumors and Their Precursor Gonadal Lesions in Patients with XY-DSD: A Case Series and Review of the Literature.

机构信息

Department of Women's Health, Tübingen University Hospital, Calwerstr. 7, 72076 Tübingen, Germany.

出版信息

Int J Environ Res Public Health. 2021 May 25;18(11):5648. doi: 10.3390/ijerph18115648.

Abstract

The risk of gonadal germ cell tumors is increased over the lifetime of patients with XY-disorders of sex development (XY-DSD). The aim of this study was to evaluate clinical features and histopathological outcome after gonadectomy in patients with XY-DSD to assess the risk of malignant transformation to gonadal germ cell tumors. Thirty-five women treated for XY-DSD at our hospital between 2003 and 2020 were enrolled in this study. Twenty-seven (77%) underwent prophylactic gonadectomy, 10 (29%) at our department and 17 (48%) at external hospitals. Eight (23%) patients didn't receive gonadectomy. Of the patients who underwent a surgical procedure at our hospital, two patients were diagnosed with a unilateral seminoma, one patient with a bilateral and one patient with a unilateral Sertoli cell adenoma. According to these findings, preventive gonadectomy in patients with XY-DSD should be taken into consideration. Guidelines concerning the necessity of gonadectomy to avoid malignant transformation are still lacking. The risk of malignant germ cell tumors from rudimentary gonads has not been investigated sufficiently to date, as it is mostly based on case series due to the rarity of the condition. In our study we retrospectively analyzed patients who partly underwent bilateral gonadectomy, aiming to fill this gap. Concerning the ideal point of time for gonadectomy, further studies with a higher number of patients are needed.

摘要

患有性发育障碍(DSD)的 XY 个体一生中罹患生殖细胞肿瘤的风险增加。本研究旨在评估 XY-DSD 患者行性腺切除术的临床特征和组织病理学结局,以评估恶性转化为生殖细胞肿瘤的风险。2003 年至 2020 年期间,我院共收治 35 例 XY-DSD 女性患者,入组本研究。27 例(77%)行预防性性腺切除术,其中 10 例(29%)在我院行手术,17 例(48%)在外院行手术。8 例(23%)患者未行性腺切除术。在我院行手术的患者中,2 例诊断为单侧精原细胞瘤,1 例诊断为双侧,1 例诊断为单侧支持细胞瘤。基于这些发现,应考虑对 XY-DSD 患者行预防性性腺切除术。目前仍缺乏关于行性腺切除术以避免恶性转化必要性的指南。由于该病罕见,目前主要基于病例系列研究,因此尚未充分研究原始性腺的恶性生殖细胞肿瘤风险。在本研究中,我们回顾性分析了部分行双侧性腺切除术的患者,旨在填补这一空白。关于性腺切除术的理想时机,还需要进一步的多中心研究。

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