格雷夫斯病是hiv -1感染青少年患者免疫重建炎症综合征的表现:1例报告

Liga Kornete , Ruta Terauda , Sintija Sausa , Iveta Dzivite-Krisane , Ivars Melderis , Valentina Sitkare , Baiba Rozentale , Davis Rudolfs Zakis
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引用次数: 1

摘要

虽然Graves病(GD)是青少年甲状腺功能亢进最常见的病因,但由于Graves免疫重建炎症综合征(IRIS)引起促甲状腺激素(TSH)受体自身抗体的产生,是非常罕见的。特别是对于儿科患者,对Graves’IRIS的病因和完整发病机制知之甚少。此外,严重缺乏有效治疗计划的细节。这里介绍的病例报告仅是全球儿科患者的第三个病例报告。病例介绍:我们报告了一位白人女性青少年,她最初以颈部前部不适和紧绷以及甲状腺肿大的非特异性主诉出现。根据临床、实验室和甲状腺超声检查结果,她被诊断为GD。然而,经过几个月的门诊治疗,患者的GD仍然不能完全控制单独保守治疗。直到病人第三次住院时,才发现她以前曾被诊断患有人类免疫缺陷病毒感染,并在过去的29个月里接受了高效抗逆转录病毒治疗(HAART)。因此,TSH受体自身抗体的产生和甲状腺激素的异常变化导致GD的发展,最终诊断为Graves’IRIS。最终行甲状腺全切除术。讨论/结论:本病例报告表明,充分了解患者的完整记忆和所有先前调查的结果是多么重要。临床医生应该意识到在开始或重新开始HAART治疗的儿科患者中可能存在甲状腺功能障碍和其他自身免疫或感染过程。需要进一步的研究来优化这类儿科患者的治疗。
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Graves’ disease as a manifestation of immune reconstitution inflammatory syndrome in an HIV-1-infected adolescent patient: A case report

Introduction

Although Graves' disease (GD) is the most common cause of hyperthyroidism in adolescents, it is very rare for it to result from the production of thyroid-stimulating hormone (TSH) receptor autoantibodies due to Graves' immune reconstitution inflammatory syndrome (IRIS). Especially for paediatric patients, very little is known about the aetiology and complete pathogenesis of Graves’ IRIS. Furthermore, details of a valid treatment plan are severely lacking. The case report presented here is only the third for paediatric patients worldwide.

Case presentation

We report on a Caucasian female adolescent who initially presented with non-specific complaints about discomfort and tightness in the anterior part of the neck and thyroid enlargement. Based on clinical, laboratory and thyroid ultrasound findings, she was diagnosed with GD. However, after several months of outpatient treatment, the patient's GD could still not be fully managed with conservative therapy alone. Only when the patient was hospitalized for the third time was it discovered that she had previously been diagnosed with human immunodeficiency virus infection and had received highly active antiretroviral therapy (HAART) for the previous 29 months. Consequently, the production of autoantibodies to TSH receptors and abnormal changes in thyroid hormones had led to the development of GD and her final diagnosis was established as Graves' IRIS. Ultimately, a total thyroidectomy was performed.

Discussion/conclusion

This case report demonstrates how fundamentally important it is to have full access to a patient's complete anamnesis and results of all previous investigations. Clinicians should be made aware of the potential existence of thyroid dysfunction and other autoimmune or infectious processes in paediatric patients initiating or reinitiating HAART. Further research is needed to optimize the treatment for such paediatric patients.

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来源期刊
Journal of Clinical and Translational Endocrinology: Case Reports
Journal of Clinical and Translational Endocrinology: Case Reports Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
1.10
自引率
0.00%
发文量
32
审稿时长
27 weeks
期刊介绍: The journal publishes case reports in a variety of disciplines in endocrinology, including diabetes, metabolic bone disease and osteoporosis, thyroid disease, pituitary and lipid disorders. Journal of Clinical & Translational Endocrinology Case Reports is an open access publication.
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