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首页> 外文期刊>Hong Kong Journal of Paediatrics >First Report of Wegener's Granulomatosis in a 12-year-old Boy in Iran
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First Report of Wegener's Granulomatosis in a 12-year-old Boy in Iran

机译：韦格纳肉芽肿病的第一篇报道在伊朗的一个12岁男孩中

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The aim of this report is to describe the first instance of Wegner's granulomatosis (WG) in a 12-year-old boy at the Children's Medical Center in Tehran University. This report will analyse the variety of clinical manifestations observed in a 12-year-old boy who suffered sinobronchitis for two months before diagnosis. We present a 12-year-old patient who exhibited pathological symptoms of WG prior to diagnosis and treatment. Our patient was monitored for one year after initial therapy through the outpatients department of the Children's Medical Center in Tehran University. One year after treatment, the patient's WG appeared to be in complete remission and he remained entirely well. Although Wegener's granulomatosis is a rare condition in children and can accordingly be confused with more common ailments, accurate and timely diagnosis can be made based on an established record of clinicopathologic features of the disease, and confirmed by biopsy of nasal mucosa.
机译：本报告的目的是描述德黑兰大学儿童医学中心一名12岁男孩中Wegner肉芽肿病的首次发病。该报告将分析在诊断前患有鼻支气管炎两个月的12岁男孩的各种临床表现。我们介绍了一名12岁的患者，在诊断和治疗之前表现出WG的病理症状。最初治疗后，我们的患者通过德黑兰大学儿童医学中心的门诊部门进行了一年的监护。治疗一年后，该患者的WG似乎完全缓解，并且他仍然完全康复。尽管韦格纳肉芽肿病在儿童中很少见，因此可以与更常见的疾病相混淆，但可以根据已建立的疾病临床病理特征记录进行准确，及时的诊断，并通过鼻粘膜活检证实。

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