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Terson syndrome and leukemia: a case report

BACKGROUND: Terson syndrome is defined as intraocular hemorrhage associated with intracranial bleeding. This syndrome can occur in the event of intracranial hemorrhage or elevated intracranial pressure. To our knowledge, it has never been associated with chronic myeloid leukemia. A 45-year-old woman...

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Autores principales: Lorenzi, Umberto, Buschini, Elisa, Fea, Antonio, Machetta, Federica, Grignolo, Federico Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979781/
https://www.ncbi.nlm.nih.gov/pubmed/24729684
http://dx.doi.org/10.2147/OPTH.S52548
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author Lorenzi, Umberto
Buschini, Elisa
Fea, Antonio
Machetta, Federica
Grignolo, Federico Maria
author_facet Lorenzi, Umberto
Buschini, Elisa
Fea, Antonio
Machetta, Federica
Grignolo, Federico Maria
author_sort Lorenzi, Umberto
collection PubMed
description BACKGROUND: Terson syndrome is defined as intraocular hemorrhage associated with intracranial bleeding. This syndrome can occur in the event of intracranial hemorrhage or elevated intracranial pressure. To our knowledge, it has never been associated with chronic myeloid leukemia. A 45-year-old woman suffering from chronic myeloid leukemia was referred to our clinic with Terson syndrome after intracranial bleeding. We followed this patient for a year, performing visual acuity assessment, fundus examination, color retinography, and A-scan and B-scan ultrasonography. At presentation, her best-corrected visual acuity on the right was 20/63 and on the left was 20/320. In the right eye, retinoscopy showed blurring of the optic margins surrounded by retinal and preretinal hemorrhages, preretinal fibrosis of the optic disc along the vascular arcades, and perivascular retinal infiltrates. In the left eye, the optic disc was surrounded by retinal and preretinal hemorrhages, and massive fibrosis with hard exudates and severe preretinal hemorrhage were observed at the posterior pole. Roth spots and many circular hemorrhages were noted at the periphery of the retina. A-scan and B-scan ultrasonography did not show intraocular leukemic infiltration. The clinical picture remained stable over the following 12 months. In this patient, we observed the ophthalmoscopic features of chronic myeloid leukemia, but also coexistence of features typical of Terson syndrome. To our knowledge, no similar cases have been reported previously.
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spelling pubmed-39797812014-04-11 Terson syndrome and leukemia: a case report Lorenzi, Umberto Buschini, Elisa Fea, Antonio Machetta, Federica Grignolo, Federico Maria Clin Ophthalmol Case Report BACKGROUND: Terson syndrome is defined as intraocular hemorrhage associated with intracranial bleeding. This syndrome can occur in the event of intracranial hemorrhage or elevated intracranial pressure. To our knowledge, it has never been associated with chronic myeloid leukemia. A 45-year-old woman suffering from chronic myeloid leukemia was referred to our clinic with Terson syndrome after intracranial bleeding. We followed this patient for a year, performing visual acuity assessment, fundus examination, color retinography, and A-scan and B-scan ultrasonography. At presentation, her best-corrected visual acuity on the right was 20/63 and on the left was 20/320. In the right eye, retinoscopy showed blurring of the optic margins surrounded by retinal and preretinal hemorrhages, preretinal fibrosis of the optic disc along the vascular arcades, and perivascular retinal infiltrates. In the left eye, the optic disc was surrounded by retinal and preretinal hemorrhages, and massive fibrosis with hard exudates and severe preretinal hemorrhage were observed at the posterior pole. Roth spots and many circular hemorrhages were noted at the periphery of the retina. A-scan and B-scan ultrasonography did not show intraocular leukemic infiltration. The clinical picture remained stable over the following 12 months. In this patient, we observed the ophthalmoscopic features of chronic myeloid leukemia, but also coexistence of features typical of Terson syndrome. To our knowledge, no similar cases have been reported previously. Dove Medical Press 2014-04-03 /pmc/articles/PMC3979781/ /pubmed/24729684 http://dx.doi.org/10.2147/OPTH.S52548 Text en © 2014 Lorenzi et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Case Report
Lorenzi, Umberto
Buschini, Elisa
Fea, Antonio
Machetta, Federica
Grignolo, Federico Maria
Terson syndrome and leukemia: a case report
title Terson syndrome and leukemia: a case report
title_full Terson syndrome and leukemia: a case report
title_fullStr Terson syndrome and leukemia: a case report
title_full_unstemmed Terson syndrome and leukemia: a case report
title_short Terson syndrome and leukemia: a case report
title_sort terson syndrome and leukemia: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979781/
https://www.ncbi.nlm.nih.gov/pubmed/24729684
http://dx.doi.org/10.2147/OPTH.S52548
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