儿童期的眼眶疾病

来源 :世界核心医学期刊文摘.眼科学分册 | 被引量 : 0次 | 上传用户:wb95879981
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Background: Orbital diseases in childhood are rare and differ from orbital lesions occuring in adults. Most paediatric orbital tumours are benign,but rapid tumour growth can nevertheless threaten vision or lives. Patients: Retrospectively,we analyzed data of 41 consecutive patients with orbital disease,treated in our hospital between 2000 and 2004. The data was evaluated using descriptive statistics and case reports. Results: All children (from neonatals up to 16 years of age) with orbital disease were included in the study. The most common benign disease of the entire collective was an epidermal cyst (n=18),followed by orbital capillary haemangioma (n=4) in children under 3 years,and preseptal cellulitis in children older than 3 years. 5 patients were treated for malignant tumours,of which one patient under 3 years had an orbital metastasis of an abdominal neuroblastoma. Conclusion: Awareness of orbital diseases in childhood,as a rare entity,is crucial for timely diagnosis and appropriate treatment,to save the vision and lives of affected children. Background: Orbital diseases in childhood are rare and differ from orbital lesions occuring in adults. Most paediatric orbital tumors are benign, but rapid tumor growth can nevertheless threaten vision or lives. Patients: Retrospectively, we analyzed data of 41 consecutive patients with orbital disease, treated in our hospital between 2000 and 2004. The data was evaluated using descriptive statistics and case reports. Results: All children (from neonatals up to 16 years of age) with orbital disease were included in the study. The most common benign disease of the all collective was an epidermal cyst (n = 18), followed by orbital capillary haemangioma (n = 4) in children under 3 years, and preseptal cellulitis in children older than 3 years. 5 patients were treated for malignant tumors, of which one patient under 3 years had an orbital metastasis of an abdominal neuroblastoma. Conclusion: Awareness of orbital diseases in childhood, as a rare entity, is crucial for timely diagnosis and appropr iate treatment, to save the vision and lives of affected children.
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