Department of Radiology, Guy's and St. Thomas' NHS Foundation Trust, London, UK.
Department of Radiology, Royal Brompton and Harefield NHS Foundation Trust, London, UK.
Br J Radiol. 2021 Mar 1;94(1119):20200914. doi: 10.1259/bjr.20200914. Epub 2020 Dec 22.
Granulomatosis with polyangiitis is a rare autoimmune condition which causes respiratory tract granulomas, small to medium vessel vasculitis and renal disease. Head and neck manifestations are some of the most common presentations of the condition, with a significant proportion of patients experiencing sinonasal disease alone. The recognition of suggestive imaging findings, in combination with clinical history and serology, aids the diagnosis and appropriate treatment. This pictorial review describes and illustrates the head and neck imaging features of granulomatosis with polyangiitis, highlighting the range of CT and MRI findings of upper aerodigestive tract, orbital and skull-base disease. Recognition of the radiological appearances is of importance, since clinical presentations may be non-specific and limited disease may have negative serology. Imaging features may overlap with other pathologies so important differential diagnoses will be considered, and these are particularly relevant in the context of treatment resistance.
肉芽肿性多血管炎是一种罕见的自身免疫性疾病,可导致呼吸道肉芽肿、小到中等血管血管炎和肾脏疾病。头颈部表现是该疾病最常见的表现之一,很大一部分患者仅出现鼻-鼻窦疾病。提示性影像学发现与临床病史和血清学相结合有助于诊断和适当治疗。本影像学综述描述并说明了肉芽肿性多血管炎的头颈部影像学特征,重点介绍了上呼吸道、眼眶和颅底疾病的 CT 和 MRI 表现范围。认识到这些影像学表现非常重要,因为临床症状可能不典型,局限性疾病可能血清学检查为阴性。影像学表现可能与其他病理学重叠,因此将考虑重要的鉴别诊断,这些鉴别诊断在治疗抵抗的情况下尤其相关。