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乌干达癌症研究所收治的视网膜母细胞瘤患儿的临床表现及治疗结果

Clinical presentation and outcomes in children with retinoblastoma managed at the Uganda Cancer Institute.

作者信息

Kalinaki Abubakar, Muwonge Haruna, Balagadde-Kambugu Joyce, Mulumba Yusuf, Ntende Jacob, Ssali Grace, Nakiyingi Lydia, Nakanjako Damalie, Nalukenge Caroline, Ampaire Anne M

机构信息

Department of Ophthalmology, College of Health Sciences, Makerere University, P. O. Box 7072, Kampala, Uganda.

Habib Medical School, Islamic University in Uganda, Uganda.

出版信息

J Cancer Epidemiol. 2022 Mar 8;2022:8817215. doi: 10.1155/2022/8817215. eCollection 2022.

Abstract

BACKGROUND

The majority of patients with retinoblastoma, the most common intraocular cancer of childhood, are found in low-and middle-income countries (LMICs), with leukocoria being the most common initial presenting sign and indication for referral. Findings from the current study serve to augment earlier findings on the clinical presentation and outcomes of children with retinoblastoma in Uganda.

METHODS

This was a retrospective study in which we reviewed records of children admitted with a diagnosis of retinoblastoma at the Uganda Cancer Institute from January 2009 to February 2020. From the electronic database, using admission numbers, files were retrieved. Patient information was recorded in a data extraction tool.

RESULTS

A total of 90 retinoblastoma patients were studied, with a mean age at the first Uganda Cancer Institute (UCI) presentation of 36.7 months. There were more males (57.8%) than females, with a male to female ratio of 1.37 : 1. The majority (54.4%) had retinoblastoma treatment prior to UCI admission. The most common presenting symptoms were leukocoria (85.6%), eye reddening (64.4%), and eye swelling (63.3%). At 3 years of follow-up after index admission at UCI, 36.7% of the patients had died, 41.1% were alive, and 22.2% had been lost to follow-up. The median 3-year survival for children with retinoblastoma in our study was 2.18 years. Significant predictors of survival in the multivariate analysis were follow-up duration ( ), features of metastatic spread ( = 0.001), history of eye swelling ( = 0.012), and bilateral enucleation ( = 0.011).

CONCLUSIONS

The majority of children who presented to the Uganda Cancer Institute were referred with advanced retinoblastoma, and there was a high mortality rate. Retinoblastoma management requires a multidisciplinary team that should include paediatric ophthalmologists, paediatric oncologists, ocular oncologists, radiation oncologists, and nurses.

摘要

背景

视网膜母细胞瘤是儿童最常见的眼内癌,大多数患者来自低收入和中等收入国家(LMICs),白瞳症是最常见的初始表现体征及转诊指征。本研究结果有助于补充早期关于乌干达视网膜母细胞瘤患儿临床表现及预后的研究发现。

方法

这是一项回顾性研究,我们回顾了2009年1月至2020年2月在乌干达癌症研究所确诊为视网膜母细胞瘤的患儿记录。通过电子数据库,利用入院编号检索病历。患者信息记录在数据提取工具中。

结果

共研究了90例视网膜母细胞瘤患者,首次在乌干达癌症研究所(UCI)就诊时的平均年龄为36.7个月。男性患者(57.8%)多于女性,男女比例为1.37∶1。大多数患者(54.4%)在入住UCI之前已接受视网膜母细胞瘤治疗。最常见的表现症状为白瞳症(85.6%)、眼红(64.4%)和眼肿(63.3%)。在UCI首次入院后3年的随访中,36.7%的患者死亡,41.1%存活,22.2%失访。本研究中视网膜母细胞瘤患儿的3年中位生存期为2.18年。多变量分析中生存的显著预测因素为随访时间( )、转移扩散特征( = 0.001)、眼肿病史( = 0.012)和双侧眼球摘除术( = 0.011)。

结论

到乌干达癌症研究所就诊的大多数儿童被诊断为晚期视网膜母细胞瘤,死亡率很高。视网膜母细胞瘤的管理需要一个多学科团队,应包括儿科眼科医生、儿科肿瘤学家、眼肿瘤学家、放射肿瘤学家和护士。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d31f/8924608/d3e9c44ad3f1/JCE2022-8817215.001.jpg

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