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The role of radiation therapy in the management of ocular reticulum cell sarcoma

โœ Scribed by Lawrence Margolis; Robert Fraser; Allen Lichter; Devron H. Char


Publisher
John Wiley and Sons
Year
1980
Tongue
English
Weight
429 KB
Volume
45
Category
Article
ISSN
0008-543X

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โœฆ Synopsis


Francisco, from 1978 through 1974. Six of the 9 patients had visual symptoms as the first manifestation of their disease. Eight of the Y patients developed intracranial lymphoma at some time during the course of the disease. Despite lymphoma work-up including bone marrow biopsies and lymphangiogram, only 1 patient was found to have documented systemic involvement. The diagnosis of ocular lymphoma was based on pathologic material from the eye in 5 cases or from central nervous system biopsy in 4 patients in association with tumor cell infiltrates in the retina and vitreous clouding. Radiation therapy to the eyes improved vision in 10 of 13 eyes treated in 8 patients. The usual dose was in the range of 3500 to 4500 rads given over 4-5 weeks. In addition, 7 patients received central nervous system irradiation. Review of the literature reinforced the findings of this series showing the frequent association of ocular lymphoma with intracranial lymphoma and the rare systemic dissemination. This disease process has previously been referred to as ocular reticulum cell sarcoma.


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Radiation therapy in the palliative mana
โœ Harold Perry; Florence C. H. Chu ๐Ÿ“‚ Article ๐Ÿ“… 1962 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 397 KB ๐Ÿ‘ 1 views

OFT TISSUE SARCOMAS are relatively uncom-S mon. The management of this group of sarcomas has been primarily surgical.1-\* Although radiation therapy has been used preoperatively, postoperatively, and for the treatment of recurrent, residual, or metastatic disease, its efficacy has not been fully ass