一名原发性空蝶鞍综合征男性患者的全垂体功能减退症和侏儒症（作者译）
[Panhypopituitarism and dwarfism in a man with a primary empty sella turcica (author's transl)].
作者信息
Turpin G, Jambart S, de Gennes J L
出版信息
Nouv Presse Med. 1979 Mar 10;8(11):847-8, 850.
PMID:450657
Abstract
Endocrine features associated with the primary empty sella turcica syndrom are rare; they are usually related to a pituitary microadenoma and more rarely to an idiopathic panhypop ituitarism. A pituitary dwarfism with an idiopathic panhypopituitarism of hypothalamic origin, associated with an "empty" sella turcica containing functional and stimulable pituitary tissue, is reported in a 27 year old male Moraccan.
摘要
与原发性空蝶鞍综合征相关的内分泌特征罕见；它们通常与垂体微腺瘤有关，更罕见的是与特发性全垂体功能减退有关。本文报道了一名27岁摩洛哥男性，患有起源于下丘脑的特发性全垂体功能减退所致的垂体性侏儒症，并伴有一个含有功能性且可刺激的垂体组织的“空”蝶鞍。
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