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Primary thyroid failure presenting as a pituitary tumour

机译:原发性甲状腺功能衰竭表现为垂体瘤

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摘要

A 20-year-old female was referred as a pituitary tumour with failure to grow. Primary hypothyroidism from the age of 8 had been diagnosed at the age of 11, when the patient was put on thyroid replacement therapy. Routine investigations showed normal anterior pituitary function, and confirmed the diagnosis of primary hypothyroidism. A needle biopsy of the pituitary gland revealed an empty fossa. The possible relation of the empty sella with the primary hypothyroidism is discussed. A chromosome anomaly, deletion of the short arm of an X chromosome, was found and its contribution to the delayed growth is discussed.
机译:一名20岁的女性被称为垂体瘤,没有生长。当患者接受甲状腺替代疗法时,已诊断出从8岁开始的原发性甲状腺功能减退症。常规检查显示垂体前叶功能正常,并确诊为原发性甲状腺功能减退症。垂体的活检显示空窝。讨论了空蝶鞍与原发性甲状腺功能减退的可能关系。发现染色体异常,即X染色体短臂的缺失,并讨论了其对延迟生长的影响。

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