Diagnosis and treatment of pediatric arterial stenosis associated with neurofibromatosis type 1.

IF 2 3区 医学 Q2 PEDIATRICS BMC Pediatrics Pub Date : 2025-01-11 DOI:10.1186/s12887-024-05240-w
Haichong Li, Hanwen Zhang, Jun Cao, Dong Guo, Xuejun Zhang, Ziming Yao
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Abstract

Background: Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder affecting multiple systems. However, arterial stenosis is a rare manifestation in patients with NF1. Since the symptoms of arterial stenosis caused by NF1 are often atypical and have a high under-diagnosis rate, this can lead to serious complications such as hypertension, ischemic stroke, or even death. The aim of our research is to analyse the clinical characteristics of arterial stenosis in pediatric patients with NF1 and to summarise its diagnosis, treatment and prognosis.

Methods: We conducted a retrospective review of data from patients with NF1 treated at Beijing Children's Hospital from 2016 to 2020. Patients diagnosed with arterial stenosis, identified through clinical symptoms, physical examination, arterial ultrasonography, or imaging studies, were included in this study. These patients received symptomatic drug and/or surgical treatments and were followed up regularly. We summarized demographic characteristics, sites of arterial stenosis, clinical manifestations, and treatment outcomes.

Result: Among the 258 patients with NF1 treated at our hospital, 12 (4.7%) had arterial stenosis, comprising 9 males and 3 females with a median age of 7 years (range: 1-14 years). Renal artery stenosis was diagnosed in 7 patients (58.3%), while internal carotid artery (ICA) stenosis was diagnosed in 5 patients (41.7%). The predominant symptoms of renal artery and ICA stenosis were renal hypertension and convulsions, respectively. Antihypertensive drugs were effective in 5 patients with renal hypertension; 2 patients required balloon dilatation of the renal artery due to inadequate response to medication. Oral antiepileptic treatment was effective in 3 patients with ICA stenosis, and encephaloduroarteriosynangiosis was effective in the remaining 2 cases. The follow-up period ranged from 2 to 6 years, with a median duration of 3 years. No deterioration or mortality was observed during the follow-up period.

Conclusions: Arterial stenosis was present in approximately 4.7% of patients with NF1, predominantly affecting the renal artery and ICA. Renal hypertension and convulsions were the primary symptoms of renal artery and ICA stenosis, respectively. Early diagnosis and intervention can substantially improve the prognosis of these patients.

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1型神经纤维瘤病相关小儿动脉狭窄的诊断与治疗。
背景:1型神经纤维瘤病(NF1)是一种常染色体显性遗传病,影响多系统。然而,动脉狭窄在NF1患者中是一种罕见的表现。由于NF1引起的动脉狭窄症状往往是非典型的,诊断率高,这可能导致严重的并发症,如高血压、缺血性中风,甚至死亡。我们的研究目的是分析小儿NF1动脉狭窄的临床特点,总结其诊断、治疗和预后。方法:回顾性分析2016 - 2020年北京儿童医院收治的NF1患儿的资料。通过临床症状、体格检查、动脉超声检查或影像学检查确诊为动脉狭窄的患者纳入本研究。这些患者接受对症药物和/或手术治疗,并定期随访。我们总结了人口统计学特征、动脉狭窄部位、临床表现和治疗结果。结果:本院收治的258例NF1患者中,有12例(4.7%)发生动脉狭窄,其中男9例,女3例,中位年龄7岁(范围1 ~ 14岁)。肾动脉狭窄7例(58.3%),颈内动脉狭窄5例(41.7%)。肾动脉和ICA狭窄的主要症状分别为肾性高血压和惊厥。5例肾性高血压患者降压药有效;2例患者由于对药物反应不足,需要肾动脉球囊扩张术。3例颈内动脉狭窄患者口服抗癫痫药物治疗有效,其余2例脑硬动脉合并症有效。随访时间为2 - 6年,中位随访时间为3年。随访期间未见病情恶化或死亡。结论:大约4.7%的NF1患者存在动脉狭窄,主要影响肾动脉和ICA。肾动脉和ICA狭窄的主要症状分别为肾高血压和惊厥。早期诊断和干预可大大改善这些患者的预后。
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来源期刊
BMC Pediatrics
BMC Pediatrics PEDIATRICS-
CiteScore
3.70
自引率
4.20%
发文量
683
审稿时长
3-8 weeks
期刊介绍: BMC Pediatrics is an open access journal publishing peer-reviewed research articles in all aspects of health care in neonates, children and adolescents, as well as related molecular genetics, pathophysiology, and epidemiology.
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