Landré Vincent, Klingebiel Felix Karl-Ludwig, van Niftrik Christiaan Hendrik Bas, Goetze Elisabeth, Speck Roberto F, Hübner Christian Thomas, Pape Hans-Christoph, Schäfer Frank Peter
Department of Traumatology, University Hospital Zurich, 8091 Zurich, Switzerland.
Department of Neurosurgery, University Hospital Zurich, 8091 Zurich, Switzerland.
J Fungi (Basel). 2025 May 9;11(5):368. doi: 10.3390/jof11050368.
Orbitocerebral mucormycosis, caused by , is a rare infection, usually occurring in tropical and subtropical climates, with a high mortality rate. We report a case of orbitocerebral mucormycosis caused by in a person living with HIV (PLWHIV) from Africa alongside a systematic literature review updating current diagnostic and treatment strategies for orbitocerebral mucormycosis caused by .
The presented case was treated in our hospital for polytrauma following a motor vehicle accident (MVA) with aggressive surgical debridement and therapy with liposomal Amphotericin B (AMB). We evaluated clinical presentation, imaging, surgery, and postoperative outcomes. A systematic review of English or German language articles (published between 1985 and 2025) was performed according to PRISMA guidelines. Articles describing patients with mucormycosis due to were summarized. Quantitative values for relevant parameters that indicated a reduction in mortality and morbidity were obtained.
The systematic search initially identified 452 publications, from which 79 studies were retrieved. Seventeen publications comprising 21 cases were included, along with one additional case from our institution, for a total of 22 rhino-orbito-cerebral infections caused by the genus . () was the most frequently isolated species (n = 17), followed by (n = 4) and (n = 1); was not reported. The majority of patients were male (72.7%), with a mean age of 40.7 ± 15.9 years. Trauma (27.3%) and diabetes mellitus (18.2%) were the most common underlying risk factors, with SARS-CoV-2 infection identified in 13.6% of cases.
Mucormycosis due to is a rare but potentially devastating condition. Based on our experience and the literature, we suggest that the early diagnosis of treated with liposomal AMB and aggressive surgical debridement is essential to reduce morbidity and mortality.
由 引起的眶脑毛霉病是一种罕见的感染,通常发生在热带和亚热带气候地区,死亡率很高。我们报告了一例来自非洲的感染人类免疫缺陷病毒(HIV)的患者发生的由 引起的眶脑毛霉病病例,并进行了系统的文献综述,以更新目前针对由 引起的眶脑毛霉病的诊断和治疗策略。
该病例在我院因机动车事故(MVA)导致多发伤接受治疗,采用积极的手术清创和脂质体两性霉素B(AMB)治疗。我们评估了临床表现、影像学检查、手术及术后结果。根据PRISMA指南对1985年至2025年间发表的英文或德文文章进行了系统综述。总结了描述因 感染毛霉病患者的文章。获取了表明死亡率和发病率降低的相关参数的定量值。
系统检索最初识别出452篇出版物,从中检索到79项研究。纳入了17篇包含21例病例的出版物,以及我院的另外1例病例,共计22例由 属引起的鼻眶脑感染。( )是最常分离出的菌种(n = 17),其次是 (n = 4)和 (n = 1);未报告 。大多数患者为男性(72.7%),平均年龄为40.7 ± 15.9岁。创伤(27.3%)和糖尿病(18.2%)是最常见的基础危险因素,13.6%的病例中发现了新型冠状病毒2感染。
由 引起的毛霉病是一种罕见但可能具有毁灭性的疾病。根据我们的经验和文献,我们建议早期诊断 并采用脂质体AMB治疗和积极的手术清创对于降低发病率和死亡率至关重要。