A rare case of 46XX,t(X;11)(q24;q23.3) with premature ovarian insufficiency

Kanchan Murarka, D. Goenka, M. L. Goenka, Parth Shah
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Abstract

Here, we report a rare case of chromosomal abnormality with translocation between bands Xq24 and 11q23.3 leading to premature ovarian insufficiency (POI). POI can occur due to various causes. Studies have shown that 10%–12% of women with POI have chromosomal abnormalities. This patient presented to us with secondary amenorrhea for the past 3 years. She had attained menarche at 13 years and had regular menstrual cycles for 9 years before suffering from secondary amenorrhea. She had no family history of POI. Her karyotype revealed 46XX,t(X;11)(q24;q23.3). Other investigations showed hypoestrogenism, raised follicle-stimulating hormone, low volume ovaries, small sized uterus, and cholelithiasis. Laparoscopic cholecystectomy was done along with pelvic laparoscopy and hysteroscopy. Sequential estrogen and progesterone was given to the patient for 3 months. Following that, in vitro fertilization with oocyte donation was done which resulted into positive beta-human chorionic gonadotropin.
罕见46XX例,t(X;11)(q24;q23.3)伴卵巢功能不全
在这里,我们报告了一例罕见的染色体异常,在Xq24和11q23.3之间易位导致卵巢早衰(POI)。POI可以由各种原因引起。研究表明,10%-12%的POI女性有染色体异常。这个病人在过去的3年里以继发性闭经向我们提出。13岁初潮,月经周期正常,9年后继发性闭经。她没有POI家族史。核型为46XX,t(X;11)(q24;q23.3)。其他调查显示雌激素水平低下、促卵泡激素升高、卵巢体积小、子宫小和胆石症。腹腔镜胆囊切除术同时行盆腔腹腔镜和宫腔镜检查。患者接受序贯雌激素和黄体酮治疗3个月。随后,用捐赠卵母细胞进行体外受精,结果β -人绒毛膜促性腺激素阳性。
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