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Progressive pituitary hyperplasia over the course of 2 years demonstrated on magnetic resonance imaging in a patient with long standing, profound primary hypothyroidism

机译:磁共振成像显示长期站立,严重原发性甲状腺功能减退的患者在2年的过程中进行性垂体增生

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Pituitary hyperplasia secondary to primary hypothyroidism and subsequent regression following thyroid replacement has been well described. We report a 12 year-old male who was retrospectively found to have progressive pituitary hyperplasia over the course of 2 years prior to his diagnosis of primary hypothyroidism, as documented on annual brain magnetic resonance imaging (MRI) for Arnold Chiari Type 1 malformation. He presented to Endocrinology with a 2-year history of fatigue, worsening daily headaches and linear growth deceleration. The diagnosis of primary hypothyroidism as the cause for his pituitary hyperplasia was made. He was started on levothyroxine with subsequent regression of pituitary hyperplasia demonstrated on repeat brain MRI six months later. This case is the first that demonstrates progressive pituitary hyperplasia from early in the course to diagnosis of hypothyroidism. It also illustrates that pituitary hyperplasia noted on routine brain MRI can be a presenting sign of primary hypothyroidism that should prompt endocrinologic evaluation.
机译:继发于原发性甲状腺功能低下的垂体增生和甲状腺置换后的随后消退已被很好地描述。我们报告了一位12岁的男性,他被诊断为原发性甲状腺功能减退症,在2年的过程中被回顾性发现垂体增生,如年度脑磁共振成像(MRI)所记录的Arnold Chiari 1型畸形。他向内分泌科介绍了2年的疲劳病史,使日常头痛恶化和线性增长减速。诊断为原发性甲状腺功能低下是垂体增生的原因。他开始使用左甲状腺素治疗,六个月后重复进行脑MRI证实垂体增生随后消失。该病例是第一个从垂体腺发育早期到甲状腺功能减退的诊断。这也说明,常规脑部MRI记录的垂体增生可能是原发性甲状腺功能减退的表现,应及时进行内分泌学评估。

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