应用NIH标准早期诊断1型神经纤维瘤病的诊断顺序。

Q2 Dentistry
Stomatologija Pub Date : 2019-01-01
Tiago Novaes Pinheiro, Fernanda Vicioni-Marques, Flavio Tendolo Fayad, Pedro Henrique Ribeiro Arantes, Juliana Arid, Mariana de Oliveira Daltoé, Fabio Marinho Furtado, Fabrício Kitazono de Carvalho
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引用次数: 0

摘要

神经纤维瘤病的早期诊断对于开始多学科治疗具有重要意义。这种综合征可能首先在儿童牙科护理中发现。本研究是关于一个9岁的病人,他被诊断为1型神经纤维瘤病,从一个丛状神经纤维瘤显示在左半上颌骨。根据美国国立卫生研究院(NIH)的诊断标准,从病变的显微诊断开始调查其他相关损伤,从而诊断出系统性改变。家长对病情的认识和多学科护理的建立对保守治疗和患者并发症的减少和生活质量的提高至关重要。在这种情况下,诊断标准的使用表明,方法学对于获得更准确和可靠的诊断是多么重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Diagnostic sequence for early diagnosis of neurofibromatosis type 1 using NIH criteria.

Early diagnosis of neurofibromatosis is significant to start the multidisciplinary approach of this type of patient. This syndrome may be first identified in pediatric dental care. This study is about a 9-year-old patient who was diagnosed with neurofibromatosis type 1 from a plexiform neurofibroma displayed in the left hemi-maxilla. From the microscopic diagnosis of the lesion the investigation of other related injuries began, according to the diagnostic criteria of the National Institute of Health (NIH), leading to the diagnosis of systemic alterations. The parental awareness about the condition and the establishment of multidisciplinary care are important for the treatment to be more conservative and the patient has fewer complications with better quality of life. The use of the diagnostic criteria in this case shows how methodization is important for reaching more accurate and reliable diagnoses.

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来源期刊
Stomatologija
Stomatologija Medicine-Medicine (all)
CiteScore
1.10
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