Suppr超能文献

眼内髓上皮瘤的临床特征及 11 例病例管理。

Intraocular medulloepithelioma clinical features and management of 11 cases.

机构信息

Department of Ophthalmology, Fudan University Eye Ear Nose and Throat Hospital, Shanghai, China.

Department of Pathology, Fudan University Eye Ear Nose and Throat Hospital, Shanghai, China.

出版信息

Br J Ophthalmol. 2024 Mar 20;108(4):566-570. doi: 10.1136/bjo-2022-322449.

Abstract

AIMS

To describe the clinical features, imaging characteristics, histopathology, treatment and outcomes of intraocular medulloepithelioma.

METHODS

Medical records of 11 patients with clinically or histopathologically confirmed medulloepithelioma were retrieved and reviewed. Clinical features, diagnostic challenges, imaging characteristics, management, histopathology and prognosis were assessed.

RESULTS

The median age of the patients at initial diagnosis was 4 years, with the most common manifestations being leukocoria (five eyes), loss of vision (four eyes), ocular pain (one eye) and ophthalmic screening (one eye). The clinical signs include a grey-white ciliary body lesion, cataract or lens subluxation, secondary glaucoma and evident cysts. The ultrasound biomicroscopy (UBM) imaging most commonly displays ciliary body mass with intratumoural cysts (nine eyes). Three patients underwent surgery for cataract or glaucoma while the tumours were incidentally found. Two of the three patients managed by eye preserve treatments eventually required enucleation because of local tumour recurrence or phthisis. One patient treated with intra-arterial chemotherapy and cryotherapy had successful tumour regression and globe salvage.

CONCLUSIONS

Initial misdiagnosis, delay in diagnosis and subsequent misdirected management is not uncommon in medulloepithelioma. The presence of multiple cysts in the tumour and retrolental neoplastic cyclitic membrane detected by UBM can offer certain information. Selective intra-arterial melphalan may prevent further tumour growth, but longer follow-up is necessary until treatment efficacy is fully evaluated.

摘要

目的

描述眼内髓上皮瘤的临床特征、影像学特征、组织病理学、治疗方法和预后。

方法

回顾性分析 11 例经临床或组织病理学证实的髓上皮瘤患者的病历资料。评估了临床特征、诊断难点、影像学特征、治疗方法、组织病理学和预后。

结果

患者的中位初诊年龄为 4 岁,最常见的表现为白瞳(5 只眼)、视力丧失(4 只眼)、眼部疼痛(1 只眼)和眼科筛查(1 只眼)。临床体征包括灰白色睫状体病变、白内障或晶状体半脱位、继发性青光眼和明显的囊肿。超声生物显微镜(UBM)成像最常见的显示睫状体肿块伴肿瘤内囊肿(9 只眼)。3 例因白内障或青光眼而行手术治疗,而肿瘤是偶然发现的。3 例接受保眼治疗的患者中,有 2 例因局部肿瘤复发或眼球萎缩而最终需要眼球摘除。1 例接受动脉内化疗和冷冻治疗的患者肿瘤成功消退并保留了眼球。

结论

髓上皮瘤患者常出现初诊误诊、诊断延误和随后的治疗方向错误。UBM 检测到肿瘤内存在多个囊肿和视网膜后肿瘤性睫状膜膜可提供一定的信息。选择性动脉内注射美法仑可能会阻止肿瘤进一步生长,但需要更长时间的随访,直到充分评估治疗效果。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验