Ribeiro N F, Cousin G C, Wilson G E, Butterworth D M, Woodwards R T
Department of Oral and Maxillofacial Surgery, North Manchester General Hospital, UK.
Int J Oral Maxillofac Surg. 2001 Apr;30(2):156-9. doi: 10.1054/ijom.2000.0010.
A case of lethal invasive mucormycosis (IM), a rare fungal infection which predominantly affects immunocompromised patients, is reported in a 73-year-old female patient who presented with a cervical abscess. The patient had asthma treated with steroids and had previously undiagnosed diabetes mellitus. Despite surgical treatment and parenteral antibiotic therapy, there was fatal progression of the condition. The pathogenesis, histological appearances and treatment of mucormycosis are discussed, particularly the importance of urgent histological examination of debrided tissue to distinguish this condition from necrotizing fasciitis (NF) earlier than microbiological culture alone would allow, thus permitting the early introduction of appropriate antifungal therapy.
报告了一例致死性侵袭性毛霉菌病(IM),这是一种罕见的真菌感染,主要影响免疫功能低下的患者,患者为一名73岁女性,表现为颈部脓肿。该患者患有哮喘,接受类固醇治疗,此前未诊断出糖尿病。尽管进行了手术治疗和肠外抗生素治疗,但病情仍出现致命进展。文中讨论了毛霉菌病的发病机制、组织学表现及治疗,尤其强调了对清创组织进行紧急组织学检查的重要性,以便比单纯依靠微生物培养更早地将这种疾病与坏死性筋膜炎(NF)区分开来,从而能够尽早开始适当的抗真菌治疗。