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1.
MEAJO-Middle East African Journal of Ophthalmology. 2010; 17 (3): 264-267
in English | IMEMR | ID: emr-123602

ABSTRACT

This study was designed to present our early experience with intravitreal bevacizumab combined with laser treatment for retinopathy of prematurity [ROP] at a single institution over a 13-month-period. A retrospective case series of eight children with ROP who received intravitreal bevacizumab combined with laser treatment between June 2007 and July 2008 were reported. A chart review was conducted to evaluate if stability of the ROP lesions had been achieved. Main information collected included data on demographics, gestational age, birth weight, length of stay in neonatal intensive care unit, and stage of ROP. Fifteen eyes of eight subjects were treated. One eye did not receive any treatment due to complete retinal detachment. The median age at treatment was 8 weeks [range, 6 weeks to 1 year]. The most common stage of ROP was 3+. All eyes remained stable at 1 year or later after treatment. Intravitreal bevacizumab in conjunction with laser treatment had promising results at our institution. We recommend prospective, randomized, controlled clinical trials to compare the effects of laser treatment alone, of bevacizumab treatment alone [at different doses], and of combined bevacizumab and laser treatment


Subject(s)
Humans , Male , Female , Antibodies, Monoclonal , Laser Therapy , Vascular Endothelial Growth Factor A , Vitreous Body , Retrospective Studies
2.
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2010; 20 (10): 692-694
in English | IMEMR | ID: emr-129237

ABSTRACT

young adult presented with acute weakness of right side of body and slurring of speech. An initial brain CT scan showed a pontine haemorrhage, however MRI done a few days later revealed a mass in the left parapharyngeal space. Histopathology of the mass revealed that it was a chondrosarcoma. Subsequently the patient was initially treated with chemotherapy and radiotherapy and later surgery. Skull base chondrosarcomabe is to be included in the differentials of a young patient presenting with signs consistent with pontine haemorrhage


Subject(s)
Humans , Male , Pons/pathology , Brain Stem/pathology , Chondrosarcoma , Skull Base Neoplasms , Skull Base , Tomography, X-Ray Computed , Magnetic Resonance Imaging
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