Rodriguez-Macias K A, Thibaud E, Houang M, Duflos C, Beldjord C, Rappaport R
Pediatric Endocrinology Unit, Hôpital des Enfants Malades, 149 rue de Sèvres, 75015 Paris, France.
Arch Dis Child. 1999 Jul;81(1):53-6. doi: 10.1136/adc.81.1.53.
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.
本文报告了7例因孤立性自主性卵巢滤泡囊肿导致假性性早熟的女孩的临床结局。7例女孩中,年龄在11个月至6.9岁之间的6例在首次急性发作时经超声检查发现单侧卵巢囊肿。仅5例患者的血浆雌二醇升高,但所有患者对促黄体生成素释放激素刺激的反应均较低。7例患者均进行了长达8年的随访,期间反复出现频率和严重程度各异的发作。仅3例患者后来出现了McCune-Albright综合征的证据。无法从初始症状或临床病程中预测该综合征。对4例患者的淋巴细胞、卵巢和骨组织进行了导致激活的G(s)α蛋白突变研究。仅1例患者的骨组织中发现了突变。由于无法通过分子研究评估体细胞突变的分布,因此对骨骼病变进行反复检查并密切随访仍然很有必要。大多数复发性卵巢囊肿患者需要采取保守治疗方法。