Vaginal bleeding: presenting symptom of acquired primary hypothyroidism in a seven year-old girl.

Y Rakover, E Weiner, E Shalev, R Luboshitsky
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Abstract

A seven year-old girl who presented with vaginal bleeding and a right ovarian cyst was diagnosed as having acquired primary hypothyroidism. She had menstruation in spite of a delayed bone age, absence of pubertal growth spurt and lack of adrenarche. Elevated levels (age-matched) of gonadotropins, normal levels of estradiol, and hyperprolactinemia were documented. The clinical and laboratory findings were reversed by thyroxin treatment. The clinical presentation in this case, and other similar descriptions in the literature, support the mechanism of pseudo-precocious puberty in untreated hypothyroidism.

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阴道出血:表现为七岁女童获得性原发性甲状腺功能减退症。
一个七岁的女孩谁提出阴道出血和右卵巢囊肿被诊断为获得性原发性甲状腺功能减退。她有月经,尽管骨龄延迟,没有青春期的生长突增和缺乏肾上腺素。高水平的促性腺激素(年龄匹配),正常水平的雌二醇,和高催乳素血症记录。甲状腺素治疗逆转了临床和实验室结果。本病例的临床表现,以及文献中其他类似的描述,支持未经治疗的甲状腺功能减退的假性性早熟机制。
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Priming with GHRH (1-29) NH2: an aid in differential diagnosis between hypothalamic and pituitary deficiencies. The new highly sensitive adrenocorticotropin assay improves detection of patients with partial adrenocorticotropin deficiency in a short-term metyrapone test. The role of TRH-stimulated prolactin responses in distinguishing gonadotropin deficiency from constitutional delayed puberty. A randomized trial of a somatostatin analog for preserving beta cell function in children with insulin dependent diabetes mellitus. Both glucagon excess and insulin deficiency characterize maturity-onset diabetes mellitus of youth (MODY).
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