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Case of mucormycosis of mandible after self-extraction of teeth incidentally detected to have chronic granulomatous disease: Case report and literature review

机译:下颌毛霉菌病自拔后偶然发现患有慢性肉芽肿病的病例:病例报告及文献复习

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摘要

Mucormycosis isolated to the mandible is a rare presentation occurring generally after dental procedures. The case we report presented with discharging sinuses over facial region with radiological appearance of isolated osteomyelitis of the mandible. The patient used to apply an addictive dental powder over his teeth leading to caries. Following this, he pulled out all his teeth, which probably led to his condition. Invasive sampling revealed mucormycosis. An extensive search for an underlying immunodeficiency revealed that the patient had chronic granulomatous disease (CGD). Despite a prolonged course of L-Amphotericin B, the patient continued to have intermittent pus discharge and surgical debridement and curettage was eventually required. The patient had a chronic course with minimal soft tissue involvement which initially did not raise the suspicion of mucormycosis. The main learning point is that an unusual invasive fungal infection in an otherwise healthy host can be the first symptom of an underlying primary immunodeficiency, like CGD. Invasive fungal infections in patients with CGD often have an indolent course.
机译:分离到下颌骨的毛霉菌病是罕见的表现,通常在牙科手术后发生。我们报告的病例表现为面部区域有鼻窦分泌物,影像学表现为下颌骨孤立性骨髓炎。病人曾经在他的牙齿上涂上成瘾的牙粉导致龋齿。此后,他拔出所有牙齿,可能导致了他的病情。侵袭性采样显示毛霉菌病。广泛搜索潜在的免疫缺陷显示该患者患有慢性肉芽肿病(CGD)。尽管L-两性霉素B病程延长,但患者仍持续出现脓液排出,最终需要进行清创术和刮除术。该患者为慢性病,软组织受累最小,起初并未引起对毛霉菌病的怀疑。主要的学习要点是,在其他方面健康的宿主中,不寻常的侵袭性真菌感染可能是潜在的原发性免疫缺陷(如CGD)的首发症状。 CGD患者的侵袭性真菌感染通常病程缓慢。

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