Karmilkar Kunal, Patel Aditi, Vaughn Troy M
Medicine, Edward Via College of Osteopathic Medicine (VCOM) - Louisiana, Monroe, USA.
Neurological Surgery, Alexandria Neurosurgical Clinic, Alexandria, USA.
Cureus. 2023 Jul 31;15(7):e42770. doi: 10.7759/cureus.42770. eCollection 2023 Jul.
Aspergillus spinal epidural abscess (ASEA) is a rare, life-threatening condition that can cause spinal cord compression with neurologic deficits. The diagnosis of ASEA can be challenging due to the atypical clinical presentation and low prevalence. We describe the successful management of a rare, immunocompetent, 85-year-old male with ASEA at the T12-L1 and L1-L2 levels and present a review of the literature. Based on most case reports and our knowledge, this is a rare presentation of ASEA in a patient without systemic symptoms, leukocytosis, or a history of immunosuppressive status due to chronic steroid use. The patient presented with multiple falls and lower extremity paraparesis with near-complete paralysis of the right lower extremity for a duration of three months. Systemic symptoms of infection were absent and standard lab evaluations were unremarkable. CT imaging identified cord signal changes at the level of T10-T11 and a contrast block at L1 suspicious for spinal stenosis and impingement. During lumbar spine exploration, purulent fluid consistent with an abscess was found in the epidural space. Cultures were forwarded to microbiology and returned with Aspergillus. Postoperatively, Infectious Disease (ID) recommended treatment with voriconazole, cefepime, and vancomycin, which yielded gradual symptom improvement. The successful management of ASEA requires a multidisciplinary approach involving neurosurgeons, infectious disease specialists, radiologists, and physical therapists. Clinicians should be aware of the possibility of ASEA regardless of systemic symptoms, and early diagnosis and prompt treatment with surgical decompression and appropriate antifungal therapy are imperative for successful management.
曲霉菌脊髓硬膜外脓肿(ASEA)是一种罕见的、危及生命的疾病,可导致脊髓受压并伴有神经功能缺损。由于临床表现不典型且发病率低,ASEA的诊断具有挑战性。我们描述了一名罕见的、免疫功能正常的85岁男性患者,其在T12-L1和L1-L2水平患有ASEA的成功治疗过程,并对相关文献进行了综述。根据大多数病例报告及我们的了解,这是一例ASEA在无全身症状、白细胞增多或因长期使用类固醇导致免疫抑制状态病史患者中的罕见表现。该患者出现多次跌倒及下肢轻瘫,右下肢近乎完全瘫痪,持续了三个月。无感染的全身症状,标准实验室检查无异常。CT成像显示T10-T11水平脊髓信号改变,L1处有强化阻滞,怀疑有椎管狭窄和压迫。在腰椎探查过程中,在硬膜外间隙发现了与脓肿相符的脓性液体。培养物送检微生物学检查,结果为曲霉菌。术后,传染病科建议使用伏立康唑、头孢吡肟和万古霉素治疗,症状逐渐改善。ASEA的成功治疗需要多学科方法,包括神经外科医生、传染病专家、放射科医生和物理治疗师。临床医生应意识到无论有无全身症状都有可能发生ASEA,早期诊断以及通过手术减压和适当的抗真菌治疗进行及时治疗对于成功治疗至关重要。