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糖皮质激素治疗后淋巴细胞性垂体炎患者发生格雷夫斯病。

Development of Graves' disease in a patient with lymphocytic hypophysitis following glucocorticoid treatment.

作者信息

Ono Yuka, Wada Norio, Baba Shuhei, Sugawara Hajime, Miyoshi Arina, Obara Shinji

出版信息

Endocrinol Diabetes Metab Case Rep. 2025 Jun 25;2025(2). doi: 10.1530/EDM-24-0145. Print 2025 Apr 1.

Abstract

SUMMARY

We report the case of a 41-year-old Japanese woman with visual field disturbances during late pregnancy. At 39 weeks of gestation, she was diagnosed with bitemporal hemianopsia at the ophthalmology department. An MRI revealed a symmetrical pituitary gland enlargement, compressing the optic chiasm. An emergency cesarean section was performed immediately, resulting in the delivery of a male infant weighing 3,112 grams. Laboratory tests indicated low serum free thyroxine (T4), thyroid-stimulating hormone (TSH), cortisol, luteinizing hormone, and follicle-stimulating hormone. The patient was clinically diagnosed with lymphocytic hypophysitis (LHy). Due to her visual field impairment, she was administered 60 mg of prednisolone daily. After 2 days, her visual field impairment improved rapidly, leading to a gradual tapering of the dose. Six months after treatment initiation, an MRI showed shrinkage of the pituitary gland. Her prednisolone dose was reduced to 5 mg daily, and she was switched to hydrocortisone at 15 mg daily. Twelve months after starting treatment, the patient developed thyrotoxicosis. Testing revealed a positive TSH receptor antibody, resulting in a diagnosis of Graves' disease (GD). Treatment with thiamazole (15 mg daily) and potassium iodide (76 mg daily) was initiated, and her thyroid function normalized after 2 months. LHy is believed to have an autoimmune mechanism and is frequently associated with other autoimmune diseases; however, the development of GD is rare. Development of Graves' disease should be considered in patients with LHy, particularly during the postpartum period and the glucocorticoid treatment process.

LEARNING POINTS

Females with lymphocytic hypophysitis often experience local symptoms, such as visual field disorders, when pregnant. This condition is frequently associated with autoimmune diseases, particularly autoimmune thyroid disorders. However, reports explicitly linking it to Graves' disease have been limited. The postpartum period is considered a trigger of the onset of Graves' disease. In addition, the high-dose glucocorticoid treatment and its tapering may affect it.

摘要

摘要

我们报告了一例41岁日本女性在妊娠晚期出现视野障碍的病例。妊娠39周时,她在眼科被诊断为双颞侧偏盲。磁共振成像(MRI)显示垂体对称增大,压迫视交叉。立即进行了紧急剖宫产,产下一名体重3112克的男婴。实验室检查显示血清游离甲状腺素(T4)、促甲状腺激素(TSH)、皮质醇、黄体生成素和卵泡刺激素水平较低。患者临床诊断为淋巴细胞性垂体炎(LHy)。由于她存在视野损害,每天给予60毫克泼尼松龙。2天后,她的视野损害迅速改善,随后剂量逐渐减少。开始治疗6个月后,MRI显示垂体缩小。她的泼尼松龙剂量减至每日5毫克,并换用每日15毫克的氢化可的松。开始治疗12个月后,患者出现甲状腺毒症。检查发现促甲状腺激素受体抗体阳性,诊断为格雷夫斯病(GD)。开始使用甲巯咪唑(每日15毫克)和碘化钾(每日76毫克)治疗,2个月后甲状腺功能恢复正常。淋巴细胞性垂体炎被认为具有自身免疫机制,且常与其他自身免疫性疾病相关;然而,并发格雷夫斯病的情况较为罕见。淋巴细胞性垂体炎患者,尤其是在产后和糖皮质激素治疗过程中,应考虑格雷夫斯病的发生。

学习要点

淋巴细胞性垂体炎女性患者在孕期常出现局部症状,如视野障碍。这种情况常与自身免疫性疾病相关,尤其是自身免疫性甲状腺疾病。然而,明确将其与格雷夫斯病联系起来的报道有限。产后被认为是格雷夫斯病发病的一个触发因素。此外,大剂量糖皮质激素治疗及其减量可能会对其产生影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cac/12207596/87d0d32009b6/EDM-24-0145fig1.jpg

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