Laboratoire de Parasitologie Mycologie, CHU Lille, University Lille, inserm U1285-CNRS UMR 8576, 59000 Lille, France.
Unité d'Infectiologie, CHU Lille, Lille, France.
J Mycol Med. 2020 Sep;30(3):101002. doi: 10.1016/j.mycmed.2020.101002. Epub 2020 May 19.
Rhino-orbital-aspergillosis (ROA) is a rare but serious disease in immunocompetent patients. Diagnosis is often delayed due to the absence of specific clinical symptoms. We describe the case of a patient who presented initially with ROA which spread progressively to the right ethmoid-sphenoid sinuses and then to the brain.
A 61-year-old patient with a history of well-controlled diabetes presented with a sudden severe decrease in right visual acuity. Cerebral MRI showed the presence of an infiltrate in the right orbital apex extending to the homolateral cavernous sinus without any cerebral involvement. A diagnosis of right orbital myositis was made and corticosteroid therapy was started. His symptoms worsened progressively leading to quasi-blindness. A new MRI showed the development of right sphenoid-ethmoid osteolytic lesions. A fungal aetiology was suspected and tests for fungal biomarkers found a β-(1-3)-D-glucan level of 99pg/ml but negative galactomannan. An ethmoid biopsy was performed for histological and mycological investigations, including the detection of Aspergillus DNA by qPCR. qPCR was positive and culture resulted in the isolation of multi-sensitive Aspergillus fumigatus. Treatment was initiated with voriconazole. Due to persistence of blindness and the appearance of a lesion extending to the right frontal lobe, surgical excision was performed followed by antifungal treatment for a total duration of 1year. The patient is currently stable, but has persistence of blindness in the right eye.
Invasive ROA is a rare but serious disease in immunocompetent patients which should be evoked in the differential diagnosis of a tumour or vasculitis. Early diagnosis is essential for optimal management.
变应性鼻-眶-真菌病(ROA)是一种在免疫功能正常的患者中罕见但严重的疾病。由于缺乏特异性临床症状,诊断常常被延误。我们描述了一位患者的病例,该患者最初表现为 ROA,随后病情逐渐进展累及右侧筛窦-蝶窦,并进一步累及大脑。
一名 61 岁的患者,有控制良好的糖尿病病史,突发右侧视力急剧下降。脑部 MRI 显示右侧眶尖有浸润,向同侧海绵窦延伸,无任何脑部受累。诊断为右侧眼眶肌炎,并开始使用皮质类固醇治疗。他的症状逐渐恶化,导致近乎失明。新的 MRI 显示右侧筛窦-蝶窦溶骨性病变的发展。怀疑真菌病因,并进行真菌生物标志物检测,β-(1-3)-D-葡聚糖水平为 99pg/ml,但半乳甘露聚糖检测为阴性。进行了鼻内活检,进行组织学和真菌学研究,包括通过 qPCR 检测曲霉 DNA。qPCR 阳性,培养结果分离出多敏性烟曲霉。给予伏立康唑治疗。由于失明持续存在,且右侧额叶出现病变,进行了手术切除,随后进行了抗真菌治疗,共 1 年。目前患者病情稳定,但右眼仍失明。
侵袭性 ROA 是一种在免疫功能正常的患者中罕见但严重的疾病,应在肿瘤或血管炎的鉴别诊断中考虑到这一疾病。早期诊断对于最佳治疗至关重要。