小儿中枢性尿崩症的病因及临床特点评价。

IF 1
Elnare Gasimova, Merih Berberoğlu, Elif Özsu, Zehra Aycan, Rukiye Uyanık, Esra Bilici, Ayşegül Ceran, Zeynep Şiklar
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引用次数: 0

摘要

目的:中枢性尿崩症(CDI)是一种罕见但重要的疾病,其病因多样,对诊断和随访提出了挑战。确定CDI患者的诊断困难将有助于确保其管理和随访的最佳方法。本研究旨在探讨儿科患者CDI的临床和病因特点。方法:对2010 - 2019年在本中心随访的0-18岁CDI患者入院及随访资料进行分析。结果:56例患者,平均诊断年龄为7.92±5.11岁,症状持续时间为8.65±21.3个月。根据病因将患者分为器质性原因,如结构异常、肿瘤、外伤(1组,n=41)和其他原因(2组,n=15)。特发性CDI患病率为16%。60.7%至少有一种垂体激素缺乏症,最常见的是促甲状腺激素缺乏症。与2组相比,1组患者的平均诊断年龄更高,症状持续时间更短,其他垂体激素缺乏的频率更高。此外,在诊断时MRI表现正常的1年后发现了生殖细胞瘤,另一名患者在诊断后5年被诊断为朗格汉斯细胞组织细胞增多症(LCH)。所有患者对替代疗法反应良好,但2例生殖细胞瘤患者在随访期间死亡。结论:在儿童年龄组,颅内器质性病变是CDI的重要病因,尽管症状期短,但确定病因可能具有挑战性和长期性。年轻时表现出长期症状史且无其他垂体激素缺乏的患者不太可能患有器质性CDI。然而,对于诸如LCH之类的器质性原因,应在所有年龄段进行评估。特发性疾病患者是进一步病因学研究的候选者,在随访期间反复颅脑成像很重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the etiological and clinical characteristics of pediatric central diabetes insipidus.

Objectives: Central diabetes insipidus (CDI) is a rare but important disease of varying etiology that poses challenges in diagnosis and follow-up. Identifying diagnostic difficulties in patients with CDI will help ensure an optimal approach to their management and follow-up. This study aimed to characterize the clinical and etiological characteristics of CDI in pediatric patients.

Methods: We analyzed the admission and follow-up data of CDI patients aged 0-18 years who were followed in our center between 2010 and 2019.

Results: The study included 56 patients with a mean age at diagnosis of 7.92 ± 5.11 years and symptom duration of 8.65 ± 21.3 months. The patients were grouped by etiology into those with organic causes, such as structural anomalies, tumors, and trauma (group 1, n=41) and other causes (group 2, n=15). The prevalence of idiopathic CDI was 16%. At least one pituitary hormone deficiency was detected in 60.7%, the most common being thyroid stimulating hormone deficiency. Patients in group 1 had a higher mean age at diagnosis, shorter symptom duration, and higher frequency of other pituitary hormone deficiencies compared to group 2. Additionally, germinoma was detected 1 year subsequent to normal MRI findings at diagnosis and another patient was diagnosed with Langerhans cell histiocytosis (LCH) 5 years after diagnosis. All patients responded well to replacement therapies, but two patients with germinoma died during follow-up.

Conclusions: In the pediatric age group, intracranial organic pathologies are an important etiology of CDI, and despite a short symptomatic period, determining the cause may be challenging and prolonged. Patients presenting at a young age with a long history of symptoms and no other pituitary hormone deficiency are unlikely to have organic CDI. However, organic causes such as LCH should be evaluated at all ages. Patients with idiopathic disease are candidates for further etiological studies, and repeated cranial imaging is important during follow-up.

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