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绝经后女性卵巢间质细胞瘤:罕见病例

Leydig Cell Tumour of Ovary in a Postmenopausal Woman: A Rare Occurrence.

作者信息

Narayan Rakshitha, Fernandes Shannon Francesca, Rao Sujaya V

机构信息

Department of Obstetrics and Gynecology, Father Muller Medical College Hospital, Mangalore, Karnataka 575002 India.

出版信息

J Obstet Gynaecol India. 2025 Apr;75(Suppl 1):566-569. doi: 10.1007/s13224-024-02035-y. Epub 2024 Jul 10.

DOI:10.1007/s13224-024-02035-y
PMID:40390961
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12085537/
Abstract

Leydig cell tumours originate from ovarian sex cord stroma and compromise less than 0.1% of all ovarian tumours. Their unregulated testosterone secretion results in hyperandrogenism and virilization. A 62year old postmenopausal Para 2 patient presented at Father Muller medical college hospital Mangalore with rapidly progressive hirsutism and alopecia since 1 year. Physical examination revealed high grade hirsutism and Internal examination revealed bulky uterus and a 4 x 4 cm right adnexal mass. Pelvic ultrasonography revealed 3.3 x 3.5centimetres right adnexal solid lesion, which was confirmed on MRI. Blood investigations revealed high serum testosterone with normal DHEA-S and serum cortisol. Low dose dexamethasone suppression test confirmed ovary to be the source of elevated testosterone. She underwent stagging laparotomy with frozen section. Frozen section revealed features of benign sex cord stromal tumours. Final histopathological examination revealed pure Leydig cell tumour with Reinke crystals without infiltrated blood vessels or nerves. While investigating a case of postmenopausal hyperandrogenism, ovarian cancers and adrenal cancers should be considered. The final diagnosis is by histopathological evaluation of the tumour which is considered as the gold standard. These postmenopausal virilizing ovarian tumours are most often benign but they require surgery which is the main stay of treatment to control the symptoms. In those patients who have an advanced disease or have recurrence, it is recommended that adjuvant chemotherapy be given.

摘要

莱迪希细胞瘤起源于卵巢性索间质,占所有卵巢肿瘤的比例不到0.1%。其睾酮分泌失调导致高雄激素血症和男性化。一名62岁、绝经后、有2次分娩史的患者自1年前起,因多毛症和脱发迅速加重,就诊于芒格洛尔的父亲穆勒医学院医院。体格检查发现重度多毛症,内诊检查发现子宫增大,右侧附件有一个4×4厘米的肿块。盆腔超声检查发现右侧附件有一个3.3×3.5厘米的实性病变,MRI检查证实了这一结果。血液检查显示血清睾酮水平升高,硫酸脱氢表雄酮(DHEA-S)和血清皮质醇水平正常。小剂量地塞米松抑制试验证实卵巢是睾酮升高的来源。她接受了分期剖腹探查术及冰冻切片检查。冰冻切片显示为良性性索间质肿瘤的特征。最终组织病理学检查显示为纯莱迪希细胞瘤,有雷氏结晶,无血管或神经浸润。在调查绝经后高雄激素血症病例时,应考虑卵巢癌和肾上腺癌。最终诊断依靠肿瘤的组织病理学评估,这被视为金标准。这些绝经后导致男性化的卵巢肿瘤大多为良性,但需要手术治疗,这是控制症状的主要治疗手段。对于那些患有晚期疾病或复发的患者,建议给予辅助化疗。

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本文引用的文献

1
An Occult Leydig Cell Tumour in a Postmenopausal Woman Presenting with Alopecia and Hirsutism: A Case Report.一名绝经后女性出现脱发和多毛症的隐匿性莱迪希细胞瘤:病例报告
touchREV Endocrinol. 2021 Apr;17(1):75-78. doi: 10.17925/EE.2021.17.1.75. Epub 2021 Apr 28.
2
Ovarian sex cord stromal tumours: analysis of the clinical and sonographic characteristics of different histopathologic subtypes.卵巢性索间质肿瘤:不同组织病理学亚型的临床和超声特征分析。
J Ovarian Res. 2021 Apr 17;14(1):53. doi: 10.1186/s13048-021-00805-0.
3
An ovarian Leydig cell tumor of ultrasound negative in a postmenopausal woman with hirsutism and hyperandrogenism: A case report.一名绝经后多毛症和高雄激素血症女性患者的超声检查阴性的卵巢莱迪希细胞瘤:病例报告
Medicine (Baltimore). 2018 Mar;97(10):e0093. doi: 10.1097/MD.0000000000010093.
4
Total testosterone levels are often more than three times elevated in patients with androgen-secreting tumours.在分泌雄激素的肿瘤患者中,总睾酮水平通常会升高三倍以上。
BMJ Case Rep. 2015 Jan 23;2015:bcr2014204797. doi: 10.1136/bcr-2014-204797.