Incidence and Management of Retinoblastoma

N. Khan, S. Khan, A. Khan, Aisha Khan, Atiqa Khan, Sobia Khan
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Abstract

This was a retrospective as well as prospective study of fifty (50) cases of retinoblastoma in series during the study period from January 2005 to December 2015, conducted at Liaquat Medical College Eye hospital and Indus Medical College Hospital, Pakistan. The average incidence of retinoblastoma in cases presented in our department was 4.5 cases per year with 0.8 cases per year bilateral and 3.7 cases per year with unilateral involvement respectively. The minimum age in this series was 15 days and maximum age was 8 years, mean age being 3.46 years. Out of these 50 cases, 27(54%) were male and 23(46%) were females. In most of the cases diagnosis was made on clinical grounds and histopathological reports of the biopsy specimens. Other measures like plain X-ray orbit, CT scan, ultrasonography (A and B Scan) and studies of blood chemistry were used where ever needed. Majority of our cases were found to be in a fairly advanced stage (an aplasia grade severe) that is extending beyond the sclera in the orbital tissues. In 4 cases cat’s eye reflex noted. Out of these cases 3 were having involvement of the other eye extensively while in 4th case the other eye was not involved at all. Of the remaining cases 11(22%) were having vitreous seeding, 16(32%) showed extension up to the sclera and 22(44%) extended to involve the orbit. Only one case presented with the involvement of regional lymph nodes. All those cases that underwent modified exonerations were sent to radio isotope center for further management with radiation and/or chemotherapy depending upon the nature of spread. One patient who had the regional lymph nodes involvement, though did not show extra ocular spread in the orbit, underwent chemotherapy following enucleations.2 cases which were diagnosed in very early stage involving the posterior retina behind equator were managed by 60 Cobalt radioactive plaques insertion over the sclera at the site of lesion, left in place till such time as advised by the oncologist of the radio isotope center. A total of 28 enucleations and 19 modified exentrations were carried out. Recurrences were noted in 13 cases, no surgery was done in these cases and they were referred to radio isotope center at Jamshoro, Pakistan for further management with radiation or chemotherapy. In this series no case was found to have distant metastasis anywhere including long bones and other viscera of the body. 12 cases were lost to follow up at different stages of management and 6 of the cases died of unknown cause.
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视网膜母细胞瘤的发病率和治疗
本研究是一项回顾性和前瞻性研究,对2005年1月至2015年12月期间在巴基斯坦Liaquat医学院眼科医院和印度河医学院医院进行的50例视网膜母细胞瘤进行了系列研究。我科视网膜母细胞瘤平均发病率为4.5例/年,其中双侧0.8例/年,单侧3.7例/年。最小年龄15天,最大年龄8岁,平均年龄3.46岁。其中男性27例(54%),女性23例(46%)。在大多数情况下,诊断是根据临床依据和活检标本的组织病理学报告。其他措施,如普通x射线轨道、CT扫描、超声检查(A和B扫描)和血液化学研究,在需要的时候也会用到。我们的大多数病例被发现处于相当晚期(发育不全严重程度),并延伸到眼眶组织的巩膜以外。4例观察到猫眼反射。在这些病例中,有3例另一只眼睛大面积受累,而第4例另一只眼睛完全没有受累。其余11例(22%)为玻璃体植入,16例(32%)延伸至巩膜,22例(44%)延伸至眼眶。仅一例表现为局部淋巴结受累。所有经过修正的免责的病例被送往放射性同位素中心,根据扩散的性质进行放射和/或化疗的进一步治疗。一名局部淋巴结受累的患者,虽然没有显示眼眶外扩散,但在眼球摘除术后接受了化疗。2例早期诊断为赤道后视网膜病变的患者,在病变部位的巩膜上植入60个钴放射性斑块,直至放射性同位素中心肿瘤学家建议的时间。共进行了28例去核和19例改良去核。13例复发,这些病例未做手术,他们被转诊到巴基斯坦Jamshoro的放射性同位素中心接受放射或化疗的进一步治疗。在这一系列病例中,没有发现远处转移,包括长骨和身体其他脏器。12例在不同治疗阶段失访,6例死亡原因不明。
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