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1
46 XX pure gonadal dysgenesis: an infrequent cause of primary amenorrhoea.46 XX单纯性腺发育不全:原发性闭经的罕见病因。
BMJ Case Rep. 2009;2009. doi: 10.1136/bcr.07.2008.0485. Epub 2009 Apr 14.
2
Chromosomally competent ovarian failure at adolescence.青春期染色体相关的卵巢功能衰竭。
J Adolesc Health Care. 1983 Dec;4(4):257-60. doi: 10.1016/s0197-0070(83)80007-2.
3
Management of phenotypic female patients with an XY karyotype.对具有XY核型的表型女性患者的管理。
J Reprod Med. 1986 Jul;31(7):611-5.
4
Further evidence for differential regulation of follicle-stimulating hormone (FSH) and luteinizing hormone (LH): increased FSH and decreased LH levels in a patient with familial pure gonadal dysgenesis.促卵泡生成素(FSH)和促黄体生成素(LH)差异调节的进一步证据:家族性单纯性腺发育不全患者中FSH水平升高和LH水平降低。
Postgrad Med J. 1992 Nov;68(805):925-7. doi: 10.1136/pgmj.68.805.925.
5
Familial ovarian dysgenesis in 46,XX females.46,XX女性的家族性卵巢发育不全
Am J Med Sci. 1980 Nov-Dec;280(3):157-66. doi: 10.1097/00000441-198011000-00004.
6
Endometrial histology and circulating levels of medroxyprogesterone acetate (MPA), estradiol, FSH and LH in women with MPA induced amenorrhoea compared with women with secondary amenorrhoea.与继发性闭经女性相比,使用醋酸甲羟孕酮(MPA)导致闭经的女性的子宫内膜组织学以及MPA、雌二醇、促卵泡生成素(FSH)和促黄体生成素(LH)的循环水平。
Acta Obstet Gynecol Scand. 1977;56(1):43-8. doi: 10.3109/00016347709158338.
7
Chromosomal complements in primary gonadal failure.原发性性腺功能减退中的染色体组成。
Obstet Gynecol. 1984 Dec;64(6):757-61.
8
[Pure gonadal dysgenesis XX and XY: observations in fifteen patients].[46,XX和46,XY单纯性腺发育不全:15例患者的观察]
Ann Endocrinol (Paris). 2005 Dec;66(6):553-6. doi: 10.1016/s0003-4266(05)82117-1.
9
Clinical features of women with resistance to luteinizing hormone.对促黄体生成素抵抗的女性的临床特征。
Clin Endocrinol (Oxf). 1999 Dec;51(6):701-7. doi: 10.1046/j.1365-2265.1999.00863.x.
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Amenorrhoea in women with non-alcoholic chronic liver disease.非酒精性慢性肝病女性的闭经
Gut. 1991 Feb;32(2):202-6. doi: 10.1136/gut.32.2.202.

引用本文的文献

1
Disorders of Sex Development: Classification, Review, and Impact on Fertility.性发育障碍:分类、综述及对生育能力的影响
J Clin Med. 2020 Nov 4;9(11):3555. doi: 10.3390/jcm9113555.
2
Pure gonadal dysgenesis (46 XX type) with a familial pattern.具有家族性模式的单纯性腺发育不全(46 XX型)。
Adv Biomed Res. 2015 Aug 10;4:162. doi: 10.4103/2277-9175.162536. eCollection 2015.

本文引用的文献

1
Amenorrhea: evaluation and treatment.闭经:评估与治疗
Am Fam Physician. 2006 Apr 15;73(8):1374-82.
2
Idiopathic premature ovarian failure in 63 young women.
Horm Res. 2006;65(2):89-95. doi: 10.1159/000091177. Epub 2006 Jan 26.
3
Sex chromosomal mosaicism in the gonads of patients with gonadal dysgenesis, but normal female or male karyotypes in lymphocytes.性腺发育不全患者性腺中的性染色体嵌合体,但淋巴细胞中的核型为正常女性或男性核型。
Am J Obstet Gynecol. 2004 Apr;190(4):1059-62. doi: 10.1016/j.ajog.2003.09.053.
4
Contemporary issues in primary amenorrhea.原发性闭经的当代问题。
Obstet Gynecol Clin North Am. 2003 Jun;30(2):287-302. doi: 10.1016/s0889-8545(03)00027-5.

46 XX单纯性腺发育不全:原发性闭经的罕见病因。

46 XX pure gonadal dysgenesis: an infrequent cause of primary amenorrhoea.

作者信息

Pertusa Salvador, Palacios Ana

机构信息

Centro Salud Cabo Huertas, C/Arpon S/N, Alicante, 03540, Spain.

出版信息

BMJ Case Rep. 2009;2009. doi: 10.1136/bcr.07.2008.0485. Epub 2009 Apr 14.

DOI:10.1136/bcr.07.2008.0485
PMID:21686785
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3027735/
Abstract

Amenorrhoea can be primary or secondary. Primary amenorrhoea is a relatively common problem among teenage girls. They usually consult their paediatrician or family doctor. This condition is present in patients with normal secondary sexual characteristics but no menarche by 16 years of age, or patients who have not had menstrual flow by age 14 and are lacking normal secondary sexual characteristics. Gonadal dysgenesis is an infrequent cause for primary amenorrhoea. In this paper, the case of a 16-year-old girl whose mother consulted their family doctor because of worries about her daughter's lack of menarche is presented. A blood test showed elevated levels of follicle stimulating hormone (FSH) and luteinising hormone (LH) and low levels of oestradiol. An abdominal ultrasound was abnormal. A diagnostic laparoscopy with biopsy of both gonads was performed. Replacement hormonal therapy was applied resulting in normal menstruations after few months. An early diagnosis is extremely important.

摘要

闭经可分为原发性和继发性。原发性闭经在青少年女孩中是一个相对常见的问题。她们通常会咨询儿科医生或家庭医生。这种情况存在于具有正常第二性征但16岁仍未初潮的患者中,或14岁仍无月经来潮且缺乏正常第二性征的患者中。性腺发育不全是原发性闭经的一个罕见原因。本文介绍了一名16岁女孩的病例,其母亲因担心女儿初潮未至而咨询了家庭医生。血液检查显示促卵泡生成素(FSH)和促黄体生成素(LH)水平升高,雌二醇水平降低。腹部超声检查结果异常。进行了诊断性腹腔镜检查并对双侧性腺进行活检。应用了替代激素疗法,几个月后月经恢复正常。早期诊断极其重要。