Raffa Paulo Eduardo Albuquerque Zito, Vencio Rafael Caiado Caixeta, Ponce Andre Costa Corral, Malamud Bruno Pricoli, Vencio Isabela Caiado, Pacheco Cesar Cozar, Costa Felipe D'Almeida, Franceschini Paulo Roberto, Medeiros Roger Thomaz Rotta, Aguiar Paulo Henrique Pires
Department of Medicine, Catanduva Medical School (FAMECA-UNIFIPA), Catanduva, São Paulo, Brazil.
Department of Medicine, Pontifical Catholic University of Goiás, Goiânia, Brazil.
Surg Neurol Int. 2021 Jun 14;12:275. doi: 10.25259/SNI_435_2021. eCollection 2021.
A spinal intramedullary abscess is a rare clinical entity in which patients classically present with a subacute myelopathy and progressive paraplegia, sensory deficits, and/or bowel and bladder dysfunction. We report the second case of spinal intramedullary abscess caused by to ever be published and the first case of its kind to be surgically managed.
A 44-year-old female presented with severe lumbar pain associated with paraparesis, incontinence, and paraplegia. She reported multiple hospital admissions and had a history of seizures, having already undergone treatment for neurotuberculosis and fungal infection of the central nervous system unsuccessfully. Nevertheless, no laboratory evidence of immunosuppression was identified on further investigation. Magnetic resonance imaging showed a D10-D11, well-circumscribed, intramedullary mass within the conus, which was hypointense on T1-weighted imaging and hyperintense on T2/STIR weighted. The patient underwent surgery for removal and biopsy of the lesion, which provided the diagnosis of an intramedullary abscess caused by , a very rare condition with only one case reported in literature so far.
intramedullary abscess is a very rare clinical entity, especially in immunocompetent patients. We highlight as an important etiology that must be considered in differential diagnosis. Critical evaluation of every case, early diagnosis, timely referral and surgical management of the abscess is essential to improve neurological outcome.
脊髓内脓肿是一种罕见的临床病症,患者通常表现为亚急性脊髓病、进行性截瘫、感觉障碍和/或肠道及膀胱功能障碍。我们报告了第二例由[病原体名称未给出]引起的脊髓内脓肿病例,这是该病例首次被发表,也是首例接受手术治疗的此类病例。
一名44岁女性出现严重腰痛,伴有双侧下肢轻瘫、尿失禁和截瘫。她曾多次住院,有癫痫病史,此前针对中枢神经系统的神经结核和真菌感染治疗均未成功。然而,进一步检查未发现免疫抑制的实验室证据。磁共振成像显示在圆锥内D10 - D11水平有一个边界清晰的髓内肿块,在T1加权成像上呈低信号,在T2/短tau反转恢复加权成像上呈高信号。患者接受了手术切除并对病变进行活检,诊断为由[病原体名称未给出]引起的髓内脓肿,这是一种非常罕见的病症,迄今为止文献中仅报道过一例。
髓内脓肿是一种非常罕见的临床病症,尤其是在免疫功能正常的患者中。我们强调[病原体名称未给出]是鉴别诊断中必须考虑的重要病因。对每个病例进行严格评估、早期诊断、及时转诊以及对脓肿进行手术治疗对于改善神经功能预后至关重要。