Kawano T, Kobayashi S, Ebizuka T, Tanaka M, Ikeda M, Hashimoto H, Hirose S
Department of Rheumatology, Juntendo University, Tokyo.
Ryumachi. 1994 Feb;34(1):54-8.
A case of systemic lupus erythematosus (SLE) complicated with hypopituitarism after steroid pulse therapy is reported. A 46-years-old-female with a history of SLE starting in 1975 was admitted to our hospital in February 1991 for lupus nephritis. Steroid pulse therapy, 1000 mg methyl-prednisolone for 3 successive days as one therapy unit, was administered. Proteinuria improved remarkably, however, general fatigue and headache appeared 2 weeks after initiation of therapy. Endocrinological examination revealed hypopituitarism including the levels of TSH, FSH, GH and ACTH. The secretion of FSH and LH gradually improved after replacement therapy of dried thyroid. MRI examination of the brain revealed an empty sella. It is known that pituitary tumor, cerebrovascular accident and autoimmune lymphocytic hypophysitis cause hypopituitarism. In this case, it is unlikely that the pulse therapy may be responsible for the infarction of the anterior pituitary artery furthermore, there has been no articles describing such incidence after steroid pulse therapy. This case may be indicative of a very rare case in which the empty sella might have been exacerbated by the pulse therapy in the causation of hypopituitarism.
本文报道了一例系统性红斑狼疮(SLE)患者在接受类固醇脉冲治疗后并发垂体功能减退的病例。一名46岁女性,自1975年起患有SLE,于1991年2月因狼疮性肾炎入住我院。给予类固醇脉冲治疗,以连续3天每日1000mg甲泼尼龙作为一个治疗单元。蛋白尿显著改善,但在治疗开始2周后出现全身乏力和头痛。内分泌检查显示垂体功能减退,包括促甲状腺激素(TSH)、促卵泡生成素(FSH)、生长激素(GH)和促肾上腺皮质激素(ACTH)水平降低。在给予干燥甲状腺替代治疗后,FSH和促黄体生成素(LH)的分泌逐渐改善。脑部MRI检查显示空蝶鞍。已知垂体肿瘤、脑血管意外和自身免疫性淋巴细胞性垂体炎可导致垂体功能减退。在该病例中,脉冲治疗不太可能导致垂体前叶动脉梗死,此外,尚无关于类固醇脉冲治疗后出现此类情况的报道。该病例可能提示一种非常罕见的情况,即空蝶鞍可能因脉冲治疗而在垂体功能减退的病因中加重。