颌区脓毒性肉芽肿病(慢性肉芽肿病= CGD)。[病例报告]。

A Herrmann, J Zöller, T Böhler, I A Born
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引用次数: 0

摘要

本文报告一罕见的慢性肉芽肿病,以下颌骨为主要表现。一个10岁男孩的临床表现为骨髓炎而无感觉异常(文森特综合征)。诊断是通过硝基蓝四氮唑试验(NBT)和证明粒细胞完全缺乏细胞色素b。在脓毒性肉芽肿病中,建议持续应用磺胺甲恶唑-曲美托啶预防感染。为了治疗感染,需要进一步使用能进入粒细胞的抗生素,如利福平和磷霉素。口腔外科手术要求仔细处理组织和严密缝合伤口。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Septic granulomatosis (chronic granulomatous disease = CGD) in the jaw area. A case report].

A rare case of chronic granulomatous disease with manifestation in the mandible is presented. A 10-year-old boy showed the clinical picture of osteomyelitis without paresthesia (Vincent syndrome). Diagnosis was done by the nitroblue tetrazolium test (NBT) and by demonstration of a complete cytochrome-b deficiency of the granulocytes. In septic granulomatosis a continuous application of Sulfamethoxazol-Trimetoprim is recommended for prophylaxis of infection. For treatment of infection further antibiotics who pass into the granulocytes like rifampicin and fosfomycin are necessary. Oral surgical procedures request a careful tissue handling and a tight wound closure.

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