Lama Manik Kumar, Gurung Pritam, Acharya Samir, Pandit Rajeev Kumar, Sharma Kamana, Pant Basant
Department of Neurosurgery, Annapurna Neurological Institute and Allied Sciences, Maitighar, Kathmandu, Nepal.
Department of Neurosurgery, Annapurna Neurological Institute and Allied Sciences, Maitighar, Kathmandu, Nepal.
Int J Surg Case Rep. 2023 Jun;107:108306. doi: 10.1016/j.ijscr.2023.108306. Epub 2023 May 12.
Orbital Apex Syndrome (OAS) are characterized by multiple symptoms, such as impaired eye movement, periorbital pain, and visual disturbance. AS symptoms may be caused by inflammation, infection, neoplasm, or a vascular lesion, potentially involving a variety of nerves, such as the optic, oculomotor, trochlear or abducens, or the ophthalmic branch of the trigeminal nerve. However, OAS caused by invasive aspergillosis in post-COVID patient is a very rare phenomenon.
A 43-year-old male with a history of diabetes mellitus and hypertension who had recently recovered from a COVID-19 infection developed blurred vision on the left eye field, followed by impaired vision on left eye field for 2 months then retro-orbital pain for a further 3 months. The blurring of vision and headache developed soon after recovering from COVID-19 and was progressive in left eye field. He denied any symptoms of diplopia, scalp tenderness, weight loss, or jaw claudication. The patient was treated with IV methylprednisolone for 3 days with as diagnosis of optic neuritis, followed by a course of oral corticosteroid therapy (prednisolone, starting at 60 mg for 2 days and then tapered for 1 month), which produced transient relief of symptoms that recurred when prednisone was discontinued. Then repeat MRI was perform with no evidence of lesion; treated again in a line of optic neuritis and symptoms relief transiently. After reoccurrence of symptoms repeat MRI was perform which showed a heterogeneously enhancing intermediate signal intensity lesion in the left orbital apex. The lesion was encasing and compressing the left optic nerve, without abnormal signal intensity or contrast enhancement within the left optic nerve either proximal or distal to the lesion. The lesion was contiguous with focal asymmetric enhancement in the left cavernous sinus. No inflammatory changes were seen in the orbital fat.
OAS due to invasive fungal infection is uncommon and most often caused by Mucorales spp., or Aspergillus, particularly in those with immunocompromising conditions or uncontrolled diabetes mellitus. In OAS due to Aspergillosis urgent treatment is necessary to avoid complications such as complete vision loss and cavernous sinus thrombosis.
OASs, represent a heterogenous group of disorders that results from a number of etiologies. OAS in a background of COVID-19 pandemic can be due to invasive Aspergillus infection as in our patient without any systemic illness and lead to miss diagnosis and delay in proper treatment.
眶尖综合征(OAS)具有多种症状,如眼球运动障碍、眶周疼痛和视力障碍。这些症状可能由炎症、感染、肿瘤或血管病变引起,可能涉及多种神经,如视神经、动眼神经、滑车神经或展神经,或三叉神经眼支。然而,新冠后患者因侵袭性曲霉病导致的OAS是一种非常罕见的现象。
一名43岁男性,有糖尿病和高血压病史,近期从新冠感染中康复,左眼视野出现视力模糊,随后左眼视野视力受损2个月,继而眶后疼痛又持续了3个月。视力模糊和头痛在从新冠康复后不久出现,并在左眼视野呈进行性发展。他否认有任何复视、头皮压痛、体重减轻或颌跛行症状。患者接受了3天的静脉注射甲泼尼龙治疗,诊断为视神经炎,随后进行了一个疗程的口服糖皮质激素治疗(泼尼松龙,开始剂量为60mg,服用2天,然后逐渐减量1个月),症状得到短暂缓解,但在停用泼尼松时症状复发。然后再次进行MRI检查,未发现病变;按照视神经炎进行再次治疗,症状再次短暂缓解。症状复发后再次进行MRI检查,显示左侧眶尖有一个不均匀强化的中等信号强度病变。该病变包绕并压迫左侧视神经,病变近端或远端的左侧视神经内均无异常信号强度或对比增强。该病变与左侧海绵窦的局灶性不对称强化相邻。眼眶脂肪未见炎症改变。
侵袭性真菌感染导致的OAS并不常见,最常见的病因是毛霉目真菌或曲霉,特别是在免疫功能低下或糖尿病控制不佳的患者中。对于曲霉病导致的OAS,必须进行紧急治疗以避免诸如完全失明和海绵窦血栓形成等并发症。
OAS是一组由多种病因引起的异质性疾病。在新冠大流行背景下的OAS可能如我们的患者一样,是由于侵袭性曲霉感染,且患者无任何全身性疾病,这可能导致误诊和延误正确治疗。