Objective: To report various intraocular conditions that mimic retinoblastoma. Methods: A review was conducted of eyeballs enucleated for suspected retinoblastoma between 2003 and 2007, and referred for histopathological confirmation. The slides of cases not histopathologically consistent with the diagnosis of retinoblastoma were reexamined. Clinical records and results of neuroimaging studies were reviewed retrospectively Results: Of the 197 eyeballs examined, 182 (92%) proved to be retinoblastoma on histological exam, while 15 (8%) from 13 patients were pseudoretinoblastomas. The age of patients ranged from 4 months to 9 years, with a mean of 35.5 months. The etiologies of the pseudoretinoblastomas were as follows: persistent primary hyperplastic vitreous (PHPV) in 5 eyeballs (33%); retinal dysplasia in 3 (20%); Coats’disease, phthisis bulbi, and vitreous hemorrhage with retinal detachment in 2 (13%) each; and granulomatous endophthalmitis in 1 (8%). Conclusion The 8% erroneous diagnosis was lower than the published rates of 10 to 20%. The common etiologies of pseudoretinoblastoma were similar to those reported.
Retinoblastoma ; Retinal Telangiectasis ; Retinal Dysplasia

Objectives: To evaluate the prevalence, etiologies, demographics, and clinical presentation of enucleated pseudoretinoblastoma. Methods: This retrospective study reviewed ocular pathology records of enucleated globes with clinically diagnosed or suspected retinoblastoma submitted to a public university ocular pathology laboratory from 2013 to 2018. Hematoxylin-eosin-stained sections of pseudoretinoblastoma cases were reevaluated, and additional clinical data were taken from hospital charts. Results: Of the 211 enucleated eyes with clinically diagnosed or suspected retinoblastoma, 202 (95.7%) had histologically confirmed retinoblastoma, while 9 (4.3%) had pseudoretinoblastoma. The most common ocular conditions mimicking retinoblastoma were retinal dysplasia (2 eyes) and persistent fetal vasculature (2 eyes). The pseudoretinoblastoma group consisted of 4 females and 5 males, and enucleated were 6 right eyes and 3 left eyes. The mean age at the time of enucleation was 3.65 years, and the mean symptom duration was 17.36 months. Leukocoria, which was noted in 4 patients, was the most frequent initial symptom. No significant difference between the pseudoretinoblastoma group and the retinoblastoma group were found in terms of sex, laterality of the enucleated eye, age at the time of enucleation, and symptom duration. Conclusion In this retrospective review, the prevalence of pseudoretinoblastoma in enucleated globes clinically suspected or diagnosed with retinoblastoma was 4.3%. Persistent fetal vasculature and retinal dysplasia were the most common pseudoretinoblastomas. Clinicians should perform a thorough clinical evaluation and judiciously utilize the available diagnostic means to differentiate retinoblastoma from pseudoretinoblastoma.
eye enucleation ; retinal dysplasia ; retinoblastoma

Retinal dysplasia is an abnormal differentiation of the retina at embryonal retina stage with proliferation of its elements into rosettes, fold, and gliosis and it is very difficulat to distinguish between the various types of intraocular disease, especilaly retinoblastoma. We experienced a case of unilateral retinal dysplasia without systemic abnormalities occurring in a 5 months old boy. It was clinically suspected Retinoblastoma, which was proved to be Retinal Dysplasia by histopathologic examination.
Gliosis ; Humans ; Infant ; Male ; Retina ; Retinal Dysplasia* ; Retinaldehyde* ; Retinoblastoma

Retinal dysplasia is an important disease in the study of retinal development. The differential diagnosis of retinal dysplasia from retinoblastoma is very difficult to make clinically, but histologically the diagnosis is made by the structure of rosettes. The authors experimentally gave trauma to retina of rats and produced retinal dysplasia; we observed under electron microscope the incomplete rosette of retinal dysplasia and the complete rosette appearing in retinoblastoma. We concluded that both rosettes are formed in developing retina with environmental or hereditary defects and did a comparative study of their characteristic fine structures.
Animals ; Diagnosis ; Diagnosis, Differential ; Rats* ; Retina ; Retinal Dysplasia* ; Retinaldehyde* ; Retinoblastoma*

Retinal dysplasia is defined as an abnormal differentiation of the retina with proliferation of its elements into resettes, folds, and gliosis. The clinical presentation is usually bilateral with a variety fo systemic abnormalities. We experienced a case of unilateral retinal dysplasia without systemic abnormalities occurring in a 2-month-old girl who underwent an enucleation of her right eye because of the possibility of retinoblastoma. We reviewed the available literatures regarding this disease.
Female ; Gliosis ; Humans ; Infant ; Retina ; Retinal Dysplasia* ; Retinaldehyde* ; Retinoblastoma

Retinal dysplasia is defined as an abnormal differentiation of the retina with proliferation of its elements into resettes, folds, and gliosis. The clinical presentation is usually bilateral with a variety fo systemic abnormalities. We experienced a case of unilateral retinal dysplasia without systemic abnormalities occurring in a 2-month-old girl who underwent an enucleation of her right eye because of the possibility of retinoblastoma. We reviewed the available literatures regarding this disease.
Female ; Gliosis ; Humans ; Infant ; Retina ; Retinal Dysplasia* ; Retinaldehyde* ; Retinoblastoma

Retinal dysplasia refers to a generally nonspecific lesion resulting from interference with the normal histogenesis of the developing retina. An earlier review of the pathogenesis of retinal dysplasia indicated that this lesion might re.sult from a wide variety of etiologic causes, including congenital retinal fold or chromosOJn;ai1 abnormality asaociated with generalized anomaly such as 13-15 trisomy syndrome etc. Recently, Ulany experimental retinal dysplasias have been induced by viral infection, irradiation or intrauterine mechanical damage. The single pathogenetic basis of retinal dysplasia appears to be associated with separation of t-the retina, during a critical stage of differentiation, from its underlying pigment epithelium which play an important role to transport nutrition and oxygen from choroid to outer retinal layers. In this experiment, authors aspirated lens material as much as possible at 5 days after birth, and administrated oxygen for 5 days in group I, 10 days in group 2 and 15 days in group 3 except for control group. Retinal dysplasias were developed in all instances, but noted lesser incidence of dysplastic formation in group 3 as compared with control or group 1 in which round and oval shaped rosettes, irregular infoldings, indifferentiated cell masses and separation of the developing retina from its normal relationship to the pigment epithelium were observed microscopically. The shape and origin of rosette in retinal dysplasia appeared to similar that of retinoblastoma in morphology.
Animals ; Choroid ; Epithelium ; Incidence ; Oxygen* ; Parturition ; Rats* ; Retina ; Retinal Dysplasia* ; Retinaldehyde* ; Retinoblastoma ; Trisomy

PURPOSE: Retinopathy of prematurity (ROP) is a disorder of developing retinal blood vessels in extremely premature infants. In the 1950's, the relationship of ROP and prolonged administraion of oxygen was demonstrated by many randomized clinical trials. After than, Oxygen use was severely restricted and the incidence of ROP was decreased. However, with the development of modern intensive care, ventilator, artificial surfactant, and other technology, the survival of extremely premature infants and incidence of ROP are increasing So we studied the time of development and risk factors of ROP. We also studied to decide the optimal time of mass screening in the preterm infants. METHODS: We studied 436 infants who was admitted in NICU of Ewha Womans Uninvesity Hospital for the treatment of RDS, prematurity or other reasons. They were examined by indirect opthalmoscope to schedule. RESULTS: 1) Among 436 infants, 49 infants (11.2%) were diagnosed as a retinopathy of prematurity. 2) The indicence of ROP increased with small gestational ages and low birth weights and the mean gestational age in the group of ROP was 30.9+/-4.0weeks and mean birth weight was 1450+/-352gms. 3) Mean age of first diagnosing time was 5.6 weeks after birth and the range of distribution was very wide. But mean age of first diagnosing time in gestational age was 36.3 weeks and it's range was narrow 4) The risk factors of ROP were prolonged use of oxygen, high concentration of oxygen with ventilator, frequent apnea, sepsis, hyaline membrane disease, bronchopulmonary dysplasia, the use of xanthine derivatives, phototherapy over than 1 week, surfactant treatment, perinatal asphyxia. CONCLUSION: Retinopathy of prematurity has a relationship with small gestational period, low birth weights, long duration of high oxygen, and other risk factors. The optimal period of mass screening in preterm infants for ROP is from 33 weeks to 36 weeks gestational age rather than chronological age after birth.
Apnea ; Appointments and Schedules ; Asphyxia ; Birth Weight ; Bronchopulmonary Dysplasia ; Female ; Gestational Age ; Humans ; Hyaline Membrane Disease ; Incidence ; Infant ; Infant, Extremely Premature ; Infant, Low Birth Weight ; Infant, Newborn ; Infant, Premature ; Critical Care ; Mass Screening ; Oxygen ; Parturition ; Phototherapy ; Retinal Vessels ; Retinopathy of Prematurity* ; Risk Factors* ; Sepsis ; Ventilators, Mechanical ; Xanthine