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

IF 0.7 Q4 ENDOCRINOLOGY & METABOLISM
Yuka Ono, Norio Wada, Shuhei Baba, Hajime Sugawara, Arina Miyoshi, Shinji Obara
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引用次数: 0

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.

糖皮质激素治疗后淋巴细胞性垂体炎患者Graves病的发展
摘要:我们报告一例41岁的日本妇女在怀孕后期视野障碍。在怀孕39周时,她在眼科被诊断为双颞偏盲。核磁共振显示对称垂体增大,压迫视交叉。立即进行了紧急剖宫产手术,生下了一名体重为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、促黄体生成素和促卵泡激素较低。临床诊断为淋巴细胞性垂体炎(LHy)。由于她的视野受损,她每天给予60毫克强的松龙。2天后,她的视野损害迅速改善,导致剂量逐渐减少。治疗开始6个月后,MRI显示脑垂体萎缩。她的强的松剂量减少到每天5mg,并改为每天15mg的氢化可的松。开始治疗12个月后,患者出现甲状腺毒症。检测显示TSH受体抗体阳性,诊断为Graves病(GD)。开始使用噻马唑(每日15mg)和碘化钾(每日76mg)治疗,2个月后甲状腺功能恢复正常。LHy被认为具有自身免疫性机制,并经常与其他自身免疫性疾病相关;然而,GD的发展是罕见的。LHy患者应考虑Graves病的发展,特别是在产后和糖皮质激素治疗过程中。学习要点:患有淋巴细胞性垂体炎的女性在怀孕时经常出现局部症状,如视野障碍。这种情况通常与自身免疫性疾病,特别是自身免疫性甲状腺疾病有关。然而,明确将其与格雷夫斯病联系起来的报道有限。产后时期被认为是格雷夫斯病发病的触发因素。此外,高剂量糖皮质激素治疗及其逐渐减少也可能对其产生影响。
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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
142
审稿时长
9 weeks
期刊介绍: Endocrinology, Diabetes & Metabolism Case Reports publishes case reports on common and rare conditions in all areas of clinical endocrinology, diabetes and metabolism. Articles should include clear learning points which readers can use to inform medical education or clinical practice. The types of cases of interest to Endocrinology, Diabetes & Metabolism Case Reports include: -Insight into disease pathogenesis or mechanism of therapy - Novel diagnostic procedure - Novel treatment - Unique/unexpected symptoms or presentations of a disease - New disease or syndrome: presentations/diagnosis/management - Unusual effects of medical treatment - Error in diagnosis/pitfalls and caveats
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