Indian Journal of Ophthalmology

BRIEF COMMUNICATION
Year
: 2015  |  Volume : 63  |  Issue : 9  |  Page : 741--742

Prenatal genetic diagnosis of retinoblastoma – clinical correlates on follow-up


Srividya Neriyanuri1, Rajiv Raman2, Pukhraj Rishi2, Kumaramanickavel Govindasamy3, VL Ramprasad3, Tarun Sharma2,  
1 Department of Optometry, Elite School of Optometry, Unit of Medical Research Foundation (In Collaboration with Birla Institute of Technology and Science, Pilani, Rajasthan), Sankara Nethralaya, Chennai, Tamil Nadu, India
2 Department of Vitreo-Retina, Shri Bhagwan Mahavir Vitreoretinal Services, Medical Research Foundation, Sankara Nethralaya, Chennai, Tamil Nadu, India
3 Department of Genetics and Molecular Biology, Vision Research Foundation, Chennai, Tamil Nadu, India

Correspondence Address:
Dr. Tarun Sharma
Shri Bhagwan Mahavir Vitreoretinal Services, Sankara Nethralaya, 18 College Road, Chennai - 600 006, Tamil Nadu
India

Abstract

Retinoblastoma is the most common malignant intraocular tumor in pediatric age group if undetected leads to ocular mortality. Prenatal diagnosis is an emerging technology to detect fatal diseases in utero such that subsequent management is planned to reduce the ocular morbidity. We describe a case demonstrating the importance of prenatal diagnosis in a child with a strong family history of retinoblastoma and importance of a long-term clinical follow-up in these cases.



How to cite this article:
Neriyanuri S, Raman R, Rishi P, Govindasamy K, Ramprasad V L, Sharma T. Prenatal genetic diagnosis of retinoblastoma – clinical correlates on follow-up.Indian J Ophthalmol 2015;63:741-742


How to cite this URL:
Neriyanuri S, Raman R, Rishi P, Govindasamy K, Ramprasad V L, Sharma T. Prenatal genetic diagnosis of retinoblastoma – clinical correlates on follow-up. Indian J Ophthalmol [serial online] 2015 [cited 2019 Nov 18 ];63:741-742
Available from: http://www.ijo.in/text.asp?2015/63/9/741/170979


Full Text

Retinoblastoma is a hereditary disease, 40% of the cases are inheritable.[1] All bilateral retinoblastoma and about 15% unilateral retinoblastoma are caused by a germinal mutation.[2] Germline mutation could be familial or could be manifest de novo. About 60% of patients with retinoblastoma have unilateral involvement.[3] Mutations in the RB1 gene are responsible for almost all cases of retinoblastoma, a small percentage (5%) of retinoblastomas are caused by deletions in the region of chromosome 13 that contains the RB1[4]

 Case Report



A 22 weeks pregnant woman came to us for advice regarding the chance of offspring getting retinoblastoma as her first child had bilateral retinoblastoma. The other offspring was 1 year and 9 months old at the time of presentation with a history of leukocoria in the left eye. She was diagnosed to have bilateral retinoblastoma; Group B in the right eye and Group D in the left eye (International Classification of Retinoblastoma classification). Systemic chemotherapy (four cycles) and external-beam radiation therapy failed to control the tumor in the left eye and hence the left eye underwent enucleation with ball implant, 8 months after presentation. The right eye was salvaged with good tumor control and the preservation of vision [Figure 1].{Figure 1}

A cytogenetic analysis done at that time revealed male karyotype with 13q14 deletion in the father, and the mother was normal. The child had female karyotype with 13q14 deletion. Parental screening with ophthalmoscopic examination was done. While the mother was found to be normal, the father revealed a retinoma in his right eye.

As direct screening by mutational analysis is time-consuming and needs more sample, prenatal cord blood was taken for molecular linkage analysis for retinoblastoma.[5] The fetus was found to have the defective RB1 allele inherited from the father [Figure 2] and hence the parents were counseled accordingly. Serial ultrasounds were done to look for intraocular tumor (calcification).[5]{Figure 2}

The child was born at 34 weeks and the first ophthalmic evaluation done on the 2nd day of life was normal. The child underwent periodic monthly examination under anesthesia until 2 years of age. At 28 months of age, she developed a tumor (Group A) in the inferonasal retinal periphery of the right eye that was treated with cryotherapy [Figure 3]. The tumor was regressed following treatment. The child continued to be under bi-monthly clinical follow-up. Visual assessment with Lea symbol charts showed the visual acuity of 20/20 in both eyes. At a recent follow-up at 7 years of age, the fundus was stable, and visual acuity maintained in both the eyes.{Figure 3}

 Discussion



Prenatal diagnosis of retinoblastoma with clinical follow-up has been reported earlier,[6] however, to the best of our knowledge, this is the first report from India to show the clinical correlate of genetic findings on a prenatal diagnosis. It is important for an ophthalmologist to determine the etiology of an unilateral case (whether it is hereditary or not) as the management of the patient (examination of fellow eye, frequency of follow-up and sometimes treatment which should be provided along with genetic counseling) may be different when compared to a bilateral case.

Prenatal genetic testing can prove useful in screening for retinoblastoma in the unborn child. In this case, already having a child with retinoblastoma (with one eye enucleated) prompted the mother to undergo a prenatal screening for the next offspring. Even though primary prevention was not possible in this situation, prenatal diagnosis with serial ultrasound scans of the fetus could help look for a tumor in the fetal eye at an early stage. If detected in utero, a fetus with retinoblastoma can be delivered early to initiate early treatment and possibly reduce the morbidity and preserve the vision. Though the child was identified to have the inherited paternal risk allele, she did not develop the tumor until 28 months of age. Hence, it is likely that these children may develop tumor at a later stage of life alarming for careful and regular long-term surveillance. Thus, prenatal diagnosis offers early detection of the tumors in the course of the disease and periodic examinations aid in eye salvage.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

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