Karaca Zuleyha, Tanriverdi Fatih, Unluhizarci Kursad, Kelestimur Fahrettin, Donmez Halil
Department of Endocrinology and Metabolism, School of Medicine, Erciyes University, Kayseri, Turkey.
Endocr Res. 2009;34(1-2):10-7. doi: 10.1080/07435800902841306.
Lymphocytic hypophysitis (LH) is an autoimmune disorder associated with the infiltration of the pituitary gland by lymphocytes leading to different degrees of hypopituitarism. Females are affected more frequently than males and the disease is usually associated with pregnancy or postpartum period.
We present a case of LH who was first diagnosed with diabetes insipidus and hyperprolactinemia. In the follow-up, the patient developed growth hormone, gonadotropin, and thyroid stimulating hormone deficiency. The typical appearance of increased stalk thickness and diffuse homogenous contrast enhancement of pituitary on magnetic resonance imaging resulted in empty sella by time.
The present case demonstrates the natural course of LH over a 13-year period in which the empty sella was the final outcome.
淋巴细胞性垂体炎(LH)是一种自身免疫性疾病,与淋巴细胞浸润垂体导致不同程度的垂体功能减退有关。女性比男性更易患病,且该疾病通常与妊娠或产后时期相关。
我们报告一例最初被诊断为尿崩症和高催乳素血症的淋巴细胞性垂体炎患者。在随访过程中,患者出现生长激素、促性腺激素和促甲状腺激素缺乏。磁共振成像显示垂体柄增厚及垂体弥漫性均匀强化的典型表现,最终导致空蝶鞍。
本病例展示了淋巴细胞性垂体炎在13年期间的自然病程,空蝶鞍是其最终结局。