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Cervicofacial actinomycosis: a long forgotten infectious complication of immunosuppression - report of a case and review of the literature

机译:颈面部放线菌病:长期以来被人们遗忘的免疫抑制感染并发症-病例报告和文献复习

摘要

Actinomycosis is a rare chronic granulomatous infection caused by Gram-positive, non-acid-fast, anaerobic to microaerophilic bacteria.We report a case of cervicofacial actinomycosis in an 86-year-old woman undergoing immunosuppressive therapy with azathioprine and prednisone for rheumatoid arthritis. She underwent a dental treatment several months earlier. The diagnosis of culture-negative actinomycosis was based on histolopathology findings and the isolation of companion bacteria. The patient was treated with amoxicillin-clavulanic acid for 3 months, which produced complete clearance of her cervicofacial actinomycosis.Our case points out the pitfalls of diagnostic procedures in actinomycosis and the ability of this rare disease to mimic other medical conditions.
机译:放线菌病是一种罕见的慢性肉芽肿性感染,是由革兰氏阳性,不耐酸,对微需氧细菌厌氧引起的。我们报道了一名86岁女性接受硫唑嘌呤和泼尼松对类风湿关节炎进行免疫抑制治疗的宫颈面部放线菌病病例。她几个月前接受了牙科治疗。培养阴性的放线菌病的诊断是基于组织病理学发现和伴生细菌的分离。该患者接受阿莫西林-克拉维酸治疗3个月,完全清除了宫颈面部放线菌病。我们的病例指出了放线菌病诊断程序的缺陷以及这种罕见疾病模仿其他疾病的能力。

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