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Mehta A et al. – Radiologic studies suggested multiple bony metastases. No other site of primary tumour was found so there was a strong possibility of it being a primary orbito–cranial neurogenic tumour. Neuroblastomas and neuroendocrine tumours are very rare in adults. The orbit is an unusual site for a primary of this nature. In addition, it is quite difficult to make a specific diagnosis in a less differentiated tumour.

Today in Oculoplastics...keeping you current

Optic Disc Diameter Increases During Acute Elevations of Intraocular Pressure
Investigative Ophthalmology and Visual Science, 11/24/09

Increased Generation of Fibrocytes in Thyroid-Associated Ophthalmopathy
Journal of Clinical Endocrinology and Metabolism, 11/24/09

A modified technique of retrograde intubation dacryocystorhinostomy for proximal canalicular obstruction
Clinical Ophthalmology, 11/23/09

Today in Oncology...keeping you current

Differential roles of matrix metalloproteinase -9 and -2 depending on proliferation or differentiation of retinoblastoma cells
Investigative Ophthalmology and Visual Science, 11/24/09

Role of the Ubiquitin-Proteasome Pathway in Down-Regulation of the Gap-Junction Protein Connexin43 by TNF-alpha in Human Corneal Fibroblasts
Investigative Ophthalmology and Visual Science, 11/20/09

OCT and In Vivo Confocal Microscopy of a Pigmented Corneal Tumor-like Lesion
Ophthalmic Surgery, Lasers and Imaging, 11/19/09

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