Natural Science

Volume 5, Issue 4 (April 2013)

ISSN Print: 2150-4091   ISSN Online: 2150-4105

Google-based Impact Factor: 0.74  Citations  h5-index & Ranking

Association of retinoblastoma with clinical and histopathological risk factors

HTML  Download Download as PDF (Size: 1553KB)  PP. 437-444  
DOI: 10.4236/ns.2013.54056    4,986 Downloads   8,286 Views  Citations

ABSTRACT

A study was conducted to see the association of retinoblastoma with age, bilaterism, Tumor size, site, grades, involvement of anterior chamber, iris, ciliary body, choroid, sclera and optic nerve, and extraocular extension. This was a retrospective descriptive analytical study. The records of the Institute of Ophthalmology, King Edward Medical University/Mayo hospital, Lahore: Pakistan January 2006-Dec 2011 was analyzed. Five years biopsies (June 2006 to June 2012) of the retinoblastoma, from the Pathology department, was retrieved to see optic nerve involvement in all the retrieved specimens. The mean age was 3.54 ± 1.686 years. There were 15 cases of bilateral retinoblastoma and 37 cases with unilateral neoplasms. The age range of bilateral tumors was 2 - 6 years while the range in unilateral tumor was 1 - 10 years male to female ratio was 1:1.5. Among 52 cases, 37 (71.2%) patients were unilateral retinoblastoma and 15 (28.28%) patients were with bilateral disease. On radiological examination of patients suffering from retinoblastoma by B-Scan (Ultrasound), there were 33 (63.5%) cases with exophytic presentation while 18 (34.6%) cases showed endophytic morphology. On clinical examinations, 28 patients presented with proptosis of (it was the most common presenting sign in our patients, accounting for about 53.8% of cases), 20 cases presented with leucocoria eye with strabismus. 29/52 patients showed involvement with optic nerve, 17 were from 1 - 3 years age and 12 were from 4 - 6 years. Statistically there was no difference in the involvement of optic nerve, disc involvement and extra ocular extension with the age of patients (p = 0.217). There was also no statistical difference seen in age and gender for but a strong association was seen with patient’s presentation, symptoms and size of the tumors and anterior chamber, iris, ciliary body, choroid, sclera and optic nerve, and extra ocular extension. We concluded that a positive association was seen with tumor size and tumor extension (optic nerve, and extraocular extension). No Association was seen with age, gender and laterality of the tumors.

Share and Cite:

Khan, A. , Bukhari, M. and Mehboob, R. (2013) Association of retinoblastoma with clinical and histopathological risk factors. Natural Science, 5, 437-444. doi: 10.4236/ns.2013.54056.

Cited by

[1] Retinoblastoma Outcomes in a Tertiary Hospital in Northern Luzon, The Philippines: A 15-Year Experience
South Asian Journal of Cancer, 2022
[2] Retinoblastoma in South Asia: A scoping review
Asian Pacific Journal of …, 2021
[3] Knockdown of lncRNA NEAT1 expression inhibits cell migration, invasion and EMT by regulating the miR‑24‑3p/LRG1 axis in retinoblastoma cells
2021
[4] Histopathological Features of Group E Retinoblastoma Eyes after Upfront Enucleation
2020
[5] Association of Clinical Presentations and Histopathological Features of Retinoblastoma in a Tertiary Eye Care Centre, Eastern Nepal
2020
[6] ANRIL acts as onco-lncRNA by regulation of microRNA-24/c-Myc, MEK/ERK and Wnt/β-catenin pathway in retinoblastoma
2019
[7] Presentation of Retinoblastoma Patients in a Missionary Eye Hospital in Nigeria
2018
[8] Predicted Trends in the Incidence of Retinoblastoma in the Asia-Pacific Region
The Asia-Pacific Journal of Ophthalmology, 2014
[9] Profile of retinoblastoma in East Java, Indonesia
2013
[10] Profile of Retinoblastoma in East Java, lndonesia
2013

Copyright © 2024 by authors and Scientific Research Publishing Inc.

Creative Commons License

This work and the related PDF file are licensed under a Creative Commons Attribution 4.0 International License.