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Macular Hole With Retinal Pigment Epithelium Hyperplasia Simulating Neoplasm
Ophthalmic Surgery, Lasers and Imaging Retina, 2006 <P>A case in which a retinal pigment epithelium migration through a stage IV macular hole onto the retinal surface simulated a retinal pigment epithelium neoplasm is described. A 69-year-old woman presented with a hyperpigmented membranous retinal surface growth temporal to a stage IV macular hole in the left eye. Clinical examination and optical
Svetlana A, Pilyugina +3 more
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Archives of Ophthalmology, 1972
Eleven primary neoplasms of the retinal pigment epithelium (RPE) were studied histopathologically. These tumors presented a variety of histologic patterns, namely mosaic, tubular, papillary, or a patternless arrangement of vacuolated or anaplastic cells.
Mark O. M. Tso, Daniel M. Albert
semanticscholar +3 more sources
Eleven primary neoplasms of the retinal pigment epithelium (RPE) were studied histopathologically. These tumors presented a variety of histologic patterns, namely mosaic, tubular, papillary, or a patternless arrangement of vacuolated or anaplastic cells.
Mark O. M. Tso, Daniel M. Albert
semanticscholar +3 more sources
CHORIO‐RETINAL RESECTION OF A NEOPLASM FROM THE HUMAN EYE
Acta Ophthalmologica, 1976 An epithelioma was removed from the iris and ciliary body of a six‐year‐old girl by a partial irido‐cyclectomy. Three months later recurrence of the tumour was seen in the equatorial zone of the fundus.Three weeks after application of transscleral cryotherapy around the neoplasm, a chorio‐retinal resection of the tumour area in the fundus was performed.
P, Algvere, E, Kock
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Latent Myeloproliferative Neoplasm May Underlie Retinal Vein Occlusion In Older Patients
Blood, 2013 Abstract Background Myeloproliferative neoplasms (MPNs) have been associated with a high incidence of thrombosis and bleeding episodes, which significantly contribute to disease-related morbidity and mortality.
Katerina Zoi +10 more
openaire +2 more sources
Retinal haemorrhage as a complication of blastic plasmacytoid dendritic cell neoplasm
The Lancet Haematology, 2021 Daniel A, Balikov +2 more
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Ophthalmic Surgery Lasers and Imaging Retina, 2022
Gorlin syndrome is a rare autosomal dominant disorder with near complete penetrance. The underlying genetic mechanism is a mutation in a tumor suppressor gene.
Ashley López-Cañizares +4 more
semanticscholar +1 more source
Gorlin syndrome is a rare autosomal dominant disorder with near complete penetrance. The underlying genetic mechanism is a mutation in a tumor suppressor gene.
Ashley López-Cañizares +4 more
semanticscholar +1 more source
121 HUMAN ADENOVIRUS 12-INDUCED RETINAL NEOPLASM IN OLIVE BABOON
Journal of Neuropathology and Experimental Neurology, 1980 N. Mukai +5 more
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Aggressive-fungating retinal hemangioblastoma
Journal of Cancer Research and Therapeutics, 2021Retinal hemangioblastomas are one of the most common and early manifestations of Von Hippel–Lindau disease. Early detection is the key in their management.
S. Menon +4 more
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CALRETICULIN MUTATION ASSOCIATED WITH BILATERAL CENTRAL RETINAL VEIN OCCLUSION IN A YOUNG WOMAN
Retinal cases & brief reports, 2021We describe a young patient with bilateral central retinal vein occlusion, found to have calreticulin mutation on work-up for hypercoagulability. Calreticulin and Janus Kinase 2 mutations are prothrombotic driver mutations in myeloproliferative neoplasms
Anna Kabanovski +3 more
semanticscholar +1 more source