首页> 外文期刊>Italian Journal of Medicine >Third cranial nerve palsy (ptosis, diplopia) accompanied by orbital swelling: case report of unusual clinical presentation of giant cell arteritis associated with polymyalgia rheumatica
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Third cranial nerve palsy (ptosis, diplopia) accompanied by orbital swelling: case report of unusual clinical presentation of giant cell arteritis associated with polymyalgia rheumatica

机译:第三颅神经麻痹(上睑下垂,复视)伴眼眶红肿:风湿性多肌痛伴发巨细胞动脉炎的临床表现不寻常的病例报告

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Introduction Giant cell arteritis (GCA) is the most common systemic vasculitis in older individuals, characterized by granulomatosus inflammation of the wall of large and medium-sized arteries. The wide spectrum of arterial sites involved leads to ischemia of different organs resulting in a wide range of clinical signs and symptoms. Temporal artery is commonly involved (temporal arteritis). Unusual patterns of presentation, such as extraocular motility disorders and orbital swelling, may be early and transient manifestations of GCA and precede the permanent visual loss due to ischemic optic neuropathy. Case report We describe a patient with uncommon manifestations of GCA consisting of transient recurrent diplopia, ptosis, orbital swelling together with more typical clinical features of the disease such as musculoskeletal manifestations (polymyalgia rheumatica) and facial pain: all signs and symptoms promptly resolved under corticosteroid therapy without relapse. Conclusions A high level of suspicion of GCA in individuals over the age of 50 years is needed to prevent the development of severe complications. Clinicians should be aware of uncommon manifestations of the disease such as head–neck swelling and ophthalmoplegia: management guidelines have stated that prompt administration of adequate dose of corticosteroids as soon as ocular manifestations of GCA are noted may almost totally prevent blindness.
机译:简介巨细胞动脉炎(GCA)是老年人中最常见的系统性血管炎,其特征是大中型动脉壁的肉芽肿性炎症。所涉及的广泛的动脉部位导致不同器官的缺血,导致广泛的临床体征和症状。颞动脉通常受累(颞动脉炎)。 GCA的早期和短暂表现可能是眼外运动障碍和眼眶肿胀等异常表现形式,并在缺血性视神经病变导致永久性视力丧失之前出现。病例报告我们描述的患者具有GCA的罕见表现,包括短暂性反复发作,复视,眼睑下垂,眼眶肿胀以及该病的更多典型临床特征,例如肌肉骨骼表现(风湿性多肌痛)和面部疼痛:在皮质类固醇激素作用下,所有症状和体征均可立即解决治疗无复发。结论为防止严重并发症的发生,需要对50岁以上的人进行GCA的高度怀疑。临床医生应注意这种疾病的罕见表现,例如头颈部肿胀和眼肌麻痹:管理指南指出,一旦发现GCA的眼部表现,立即给予足够剂量的皮质类固醇激素几乎可以完全预防失明。

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