Shah Rahul, Shanina Elena, Smith Robert G, Bhardwaj Anish
Neurology/Neurocritical Care, Bakersfield Memorial Hospital, Bakersfield, USA.
Neurology, University of Texas Medical Branch, Galveston, USA.
Cureus. 2020 Nov 7;12(11):e11370. doi: 10.7759/cureus.11370.
Coccidioidomycosis, a fungal infection caused by inhaling spores of /, is endemic to the southwestern states of the United States, Northern Mexico and some parts of Central and South America. It is primarily a pulmonary infection with less than 0.5% of symptomatic cases showing dissemination. Skin, lymph nodes and bone are the commonest sites. Neurological involvement is rare and commonly presents as strokes, abscesses or meningoencephalitis. We present the case of a previously healthy 23-year-old African American male, presented with a four-month history of progressive right upper extremity weakness that initially started with right shoulder pain followed by worsening weakness and loss of muscle mass. Electromyography (EMG) demonstrated right brachial plexopathy with moderate-to-severe active denervation changes. MRI cervical spine revealed a 9-cm contrast enhancing extradural mass extending through the neural foramen from C4-T1 roots and forming a 4-cm right apical lung mass subsequently seen on MRI of the brachial plexus. All trunks, divisions and cords were thickened, hyperintense and showed contrast enhancement on MRI. Neuromuscular ultrasound (NUS) demonstrated enlargement of peripheral nerves. Differentials prior to biopsy of the mass ranged from neurofibromas to pancoast lung tumors. Coccidioidomycosis did not figure on the initial list of differentials. Patient underwent subsequent biopsy of the extradural and lung masses that showed coccidiodes. Serum coccidioides antibody titers were elevated. The patient was treated with high-dose intravenous fluconazole and aggressive mass debridement. His weakness improved on four months follow-up evaluation with significant resolution of EMG abnormalities and decreased swelling on NUS.
球孢子菌病是一种因吸入某种真菌孢子而引起的真菌感染,在美国西南部各州、墨西哥北部以及中美洲和南美洲的一些地区呈地方性流行。它主要是一种肺部感染,有症状的病例中不到0.5%会出现播散。皮肤、淋巴结和骨骼是最常见的受累部位。神经系统受累较为罕见,通常表现为中风、脓肿或脑膜脑炎。我们报告一例既往健康的23岁非裔美国男性病例,该患者有4个月渐进性右上肢无力病史,最初始于右肩部疼痛,随后无力加重且肌肉量减少。肌电图(EMG)显示右臂丛神经病变,伴有中度至重度的主动失神经改变。颈椎MRI显示一个9厘米的硬膜外肿块,通过神经孔从C4 - T1神经根延伸,随后在臂丛神经MRI上发现形成一个4厘米的右肺尖肿块。所有的干、分支和束在MRI上均增厚、信号增强且有强化。神经肌肉超声(NUS)显示周围神经增粗。肿块活检前的鉴别诊断范围从神经纤维瘤到肺上沟瘤。球孢子菌病最初并不在鉴别诊断列表中。患者随后接受了硬膜外和肺部肿块的活检,结果显示为球孢子菌。血清球孢子菌抗体滴度升高。患者接受了大剂量静脉注射氟康唑治疗及积极的肿块清创术。在4个月的随访评估中,他的无力症状有所改善,EMG异常明显缓解,NUS显示肿胀减轻。