首页> 外文期刊>Archives of disease in childhood >Follow up of precocious pseudopuberty associated with isolated ovarian follicular cysts.
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Follow up of precocious pseudopuberty associated with isolated ovarian follicular cysts.

机译:随访与孤立的卵巢滤泡性囊肿有关的性早熟。

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The clinical outcomes of seven girls presenting with pseudosexual precocity caused by isolated autonomous ovarian follicular cysts are presented. Six of the seven girls, aged 11 months to 6.9 years, had a unilateral ovarian cyst detected by ultrasound at the first acute episode. Plasma oestradiol was raised in only five of the cases, but all had a low response to luteinising hormone releasing hormone stimulation. Follow up lasted for up to eight years with recurrent episodes of variable frequency and severity in all seven patients. Evidence of McCune-Albright syndrome appeared later in only three patients. It could not be predicted from the initial symptoms or the clinical course. Mutations of the G(s)alpha protein leading to activation were investigated in the lymphocytes and ovarian and bone tissues of four patients. Only one patient showed a mutation in bone tissue. Close follow up with repeated searches for skeletal lesions remains necessary since the distribution of somatic mutations cannot be assessed by molecular studies. Most patients with recurrent ovarian cysts require a conservative approach.
机译:介绍了由孤立的自主性卵泡囊肿引起的假性早熟的七个女孩的临床结局。七个女孩中的六个,年龄11个月至6.9岁,在第一次急性发作中通过超声检测到了单侧卵巢囊肿。血浆雌二醇仅在五种情况下升高,但是对黄体生成激素释放激素刺激的反应均较低。随访持续了长达八年的时间,所有七名患者的复发频率和严重程度均反复发作。后来只有3例患者出现了McCune-Albright综合征的证据。从最初的症状或临床过程无法预测。在四名患者的淋巴细胞,卵巢和骨组织中研究了导致激活的G(s)α蛋白的突变。只有一名患者的骨组织出现突变。由于无法通过分子研究评估体细胞突变的分布,因此有必要密切随访并重复寻找骨骼病变。大多数复发性卵巢囊肿患者需要保守治疗。

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