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Diffuse bilateral orbital inflammation in Churg- Strauss syndrome.

机译:Churg-Strauss综合征弥漫性双眼眶发炎。

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A 33-year-old man was diagnosed with asthma and within 5 weeks developed bilateral periocular swelling. Examination revealed bilateral axial proptosis with conjunctival nodules. His blood tests revealed a positive p-antineutrophil cytoplasmic autoantibody with significant eosinophilia. MRI of the orbit showed enlarged extraocular muscles, lacrimal glands, and infiltrative changes in the orbital fat. Biopsy demonstrated granulomatous inflammation with eosinophil predominance. A diagnosis of diffuse bilateral inflammation in Churg-Strauss syndrome was made and the patient responded dramatically to prednisolone with resolution of systemic and orbital findings. The second case was a 72-year-old woman with a prolonged prodromal phase of asthma, paranasal sinus disease, and bilateral orbital involvement by a process consistent with reactive lymphoid hyperplasia on initial biopsy. Three years later she developed rapidly worsening orbital disease, marked peripheral eosinophilia, and orbital biopsy showed evidence of granulomatous inflammation with marked eosinophil infiltration and vasculitic changes, and a weakly positive antineutrophil cytoplasmic autoantibody. Hence, diffuse bilateral orbital inflammation occurring in the setting of asthma and peripheral eosinophilia should raise the possibility of Churg-Strauss syndrome and warrants biopsy as early institution of therapy can reduce both systemic and ophthalmic complications.
机译:一名33岁的男子被诊断出患有哮喘,并在5周内出现双侧眼周肿胀。检查发现双侧眼轴突出伴结膜结节。他的血液检查发现阳性p-抗中性粒细胞胞浆自身抗体阳性,嗜酸性粒细胞增多。眼眶MRI显示眼外肌增大,泪腺和眼眶脂肪浸润性改变。活检显示肉芽肿性炎症以嗜酸性粒细胞为主。诊断为Churg-Strauss综合征弥漫性双侧发炎,患者对泼尼松龙的反应迅速,全身和眼眶发现均得到缓解。第二例是一名72岁的女性,前驱期延长,患有哮喘,鼻旁窦疾病和双侧眼眶受累,其过程与首次活检时的反应性淋巴样增生一致。三年后,她发展为眼眶疾病,病情迅速恶化,周围嗜酸性粒细胞增多,眼眶活检显示肉芽肿性炎症,嗜酸性粒细胞浸润和血管改变明显,抗中性粒细胞胞浆自身抗体呈弱阳性。因此,在哮喘和周围嗜酸性粒细胞增多的情况下发生的弥漫性双眼眶炎症应增加Churg-Strauss综合征的可能性,并需要进行活检,因为早期治疗可以减少全身和眼科并发症。

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