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首页> 外文期刊>Radiology >Case 112: pituitary stalk transection syndrome with ectopic posterior pituitary gland.
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Case 112: pituitary stalk transection syndrome with ectopic posterior pituitary gland.

机译:病例112:具有异位后垂体的垂体茎横断综合征。

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摘要

Midsagittal Tl-weighted MR imaging revealed a small anterior pituitary gland and an absent pituitary stalk. The ectopic posterior pituitary gland appeared as an area of high signal intensity in the midline at the median eminence (Fig 1). Coronal unenhanced and contrast material- enhanced Tl-weighted MR imaging also depicted the ectopic posterior pituitary gland; however, the pituitary stalk was still not visible, even after administration of gadopentetate dimeglumine (Magnevist; Schering, Berlin, Germany) (Figs 2, 3). Discussion Growth hormone deficiency is a common endocrinologic cause of short stature. This hormone deficiency may be idiopathic or associated with organic causes, such as tumors or surgery (1). Idiopathic growth hormone deficiency occurs sporadically and may be isolated or associated with multiple pituitary hormone deficiencies. Findings associated with hypopituitarism include breech presentation, neonatal or early onset hypoglycemia, pro- longed or severe neonatal jaundice, micropenis, and a single central incisor.
机译:矢状位Tl加权MR成像显示垂体前叶小而垂体茎缺失。异位垂体后叶腺在中线突出处显示为中线高信号强度区域(图1)。冠状未增强和对比剂增强的T1加权MR成像也描绘了异位垂体后叶腺;然而,即使使用of戊二酸二聚葡胺(Magnevist; Schering,柏林,德国),垂体柄仍不可见(图2、3)。讨论生长激素缺乏症是矮小的常见内分泌原因。这种激素缺乏症可能是特发性的,也可能与器质性原因有关,例如肿瘤或手术(1)。特发性生长激素缺乏症偶发发生,可能是孤立的或与多种垂体激素缺乏症有关。与垂体功能低下相关的发现包括臀位表现,新生儿或早期发作的低血糖症,长期或严重的新生儿黄疸,微阴茎和单个中切牙。

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