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[与卵巢肿瘤相关的多囊卵巢综合征]

[The polycystic ovary syndrome associated with ovarian tumor].

作者信息

Spremović-Radjenović S, Radosavljević A, Petković S, Matijasević S, Cvetković M, Lazović G, Popović V

机构信息

Institute of Gynaecology and Obstetrics, Belgrade.

出版信息

Srp Arh Celok Lek. 1997 Nov-Dec;125(11-12):375-7.

PMID:9480574
Abstract

Case report of a girl with PCOD (polycystic ovarian disease) and Sertoli-Leydig ovarian tumour. A sixteen-year old girl was clinically, endocrinologically, echosonographically and laparoscopically examined, and polycystic ovarian disease was diagnosed. After a two-year period she was reexamined: normal adrenal function was confirmed and left ovarian tumour was discovered echosonographically. Therefore, she was operated on and adnexectomy of the left ovarian tumour and biopsy of the right ovary were done. The histopathologic analysis revealed the Sertoli-Leydig tumour of the left ovary and polycystic degeneration of the right ovary. In conclusion, because of the greater frequency of ovarian tumours in women with PCOD, the permanent follow-up of women with PCOD is necessary.

摘要

一名患有多囊卵巢疾病(PCOD)和支持-间质细胞瘤的女孩的病例报告。对一名16岁女孩进行了临床、内分泌、超声和腹腔镜检查,诊断为多囊卵巢疾病。两年后对她进行复查:确认肾上腺功能正常,超声检查发现左侧卵巢肿瘤。因此,她接受了手术,切除了左侧卵巢肿瘤并对右侧卵巢进行了活检。组织病理学分析显示左侧卵巢为支持-间质细胞瘤,右侧卵巢为多囊性退变。总之,由于患有PCOD的女性卵巢肿瘤发生率较高,对患有PCOD的女性进行长期随访是必要的。

相似文献

1
[The polycystic ovary syndrome associated with ovarian tumor].[与卵巢肿瘤相关的多囊卵巢综合征]
Srp Arh Celok Lek. 1997 Nov-Dec;125(11-12):375-7.
2
[Sertoli-Leydig cell tumour (arrhenoblastoma) in a patient with polycystic ovary syndrome: clinical, ultrasonographic, hormonal and histopathological evaluation].[多囊卵巢综合征患者的支持-间质细胞瘤(男性细胞瘤):临床、超声、激素及组织病理学评估]
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Stein-Leventhal syndrome with masculinizing ovarian tumors. Report of 3 cases.伴有男性化卵巢肿瘤的 Stein-Leventhal 综合征。3 例报告。
Obstet Gynecol. 1969 Dec;34(6):861-6.
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Malignant ovarian Sertoli-Leydig cell tumor localized with selective ovarian vein sampling.卵巢恶性 Sertoli-Leydig 细胞肿瘤经选择性卵巢静脉采样定位。
J Minim Invasive Gynecol. 2012 Nov-Dec;19(6):789-93. doi: 10.1016/j.jmig.2012.08.006.
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An ovarian Sertoli-Leydig cell tumour in a 40 year old Ethiopian woman: case report.一名40岁埃塞俄比亚女性的卵巢支持-间质细胞瘤:病例报告。
Ethiop Med J. 2000 Jul;38(3):185-90.
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[An unusual virilizing association: arrhenoblastoma and Stein-Leventhal syndrome].[一种不寻常的男性化关联:卵巢支持间质细胞瘤与多囊卵巢综合征]
G Clin Med. 1974 Nov;55(11):759-71.
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[Sertoli-Leydig tumor. Clinical case].[支持-间质细胞瘤。临床病例]
Rev Med Chil. 1999 Jul;127(7):835-8.
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[Hirsutism].[多毛症]
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Can treatment for polycystic ovarian disease induce ovarian tumour? A case report.多囊卵巢疾病的治疗会诱发卵巢肿瘤吗?一例病例报告。
J Clin Diagn Res. 2014 Jan;8(1):191-2. doi: 10.7860/JCDR/2014/7011.3964. Epub 2014 Jan 12.
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Sertoli-Leydig cell tumor - a rare androgen secreting ovarian tumor in postmenopausal women. Case report and review of literature.支持-间质细胞瘤——一种绝经后女性罕见的分泌雄激素的卵巢肿瘤。病例报告及文献复习。
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