Results 251 to 260 of about 614,157 (313)

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.
Peep V. Algvere, Erik Kock
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Pathological Condition of the Retinal Pigment Epithelium

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.
Daniel M. Albert, Maj Mark O.M. Tso
openaire   +4 more sources

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
Darius M. Moshfeghi, Peter K. Kaiser, Jason A. Goldsmith, Svetlana A. Pilyugina   +3 more
openaire   +4 more sources

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.
Christine Zoi, Argyri Gialeraki, Andreas Giannopoulos, Niki Rougkala, Katerina Zoi, Panagiotis G. Theodosiadis, Nicholas C.P. Cross, Kassiani Giannaki, Marianna Politou, Dimitris Loukopoulos, John Vergados   +10 more
openaire   +3 more sources

Retinal haemorrhage as a complication of blastic plasmacytoid dendritic cell neoplasm

The Lancet Haematology, 2021
Daniel A. Balikov, Dale L. Bixby, Rajesh C. Rao   +2 more
openaire   +4 more sources

A Malignant, Melanotic Neoplasm of the Uterus, Resembling the “Retinal Anlage” Tumors: Report of a Case

American Journal of Clinical Pathology, 1957
Dale M. Schulz
openaire   +4 more sources

121 HUMAN ADENOVIRUS 12-INDUCED RETINAL NEOPLASM IN OLIVE BABOON

Journal of Neuropathology and Experimental Neurology, 1980
Teruo Nishida, B. Cummins, Noritsugu Mukai, S. Kalter, V. Matthews, T. Nakajima   +5 more
openaire   +3 more sources

Gorlin Syndrome Associated With a Solitary Circumscribed Retinal Astrocytic Proliferation in a Pediatric Patient.

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, Hasenin Al-khersan, Piero Carletti, C. Shields, A. Berrocal   +4 more
semanticscholar   +1 more source

Acute Bilateral Retinal Vasculitis Revealing a Serotonin-Secreting Neuroendocrine Neoplasm

Pancreas, 2017
Vincent Gualino, Vincent Soler, Grégory Pugnet, Leonardo Astudillo   +3 more
openaire   +3 more sources

Aggressive-fungating retinal hemangioblastoma

Journal of Cancer Research and Therapeutics, 2021
Retinal 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, G. Ramachandran, Mridula Jacob, Ajay Hegde, K. Pai   +4 more
semanticscholar   +1 more source