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Auteur Amanda Hunter
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Ajouter le résultat dans votre panier Affiner la rechercheCase Report: Glaucoma-associated Peripapillary Retinoschisis with Corresponding Lamina Cribrosa Defect / Justin D. Roberts in OVS : Optometry & Vision Science, vol. 97, 02 (Février 2020)
[article]
in OVS : Optometry & Vision Science > vol. 97, 02 (Février 2020)
Titre : Case Report: Glaucoma-associated Peripapillary Retinoschisis with Corresponding Lamina Cribrosa Defect Type de document : article de périodique Auteurs : Justin D. Roberts ; Amanda Hunter ; Joseph Mega ; Thomas Cesaro ; Paul B. Greenberg Année de publication : 2020 Langues : Français (fre) Descripteurs (mots clés) : [Thésaurus Mesh]Glaucome à angle ouvert
[Thésaurus Mesh]Macula
[Thésaurus Mesh]Présentations de cas
[Thésaurus Mesh]Tomographie par cohérence optiqueMots-clés : case reports rétinoschisis péripapillaire glaucoma lamina cribrosa tomography, optical coherence glaucoma, open-angle Résumé : SIGNIFICANCE: Peripapillary retinoschisis is associated with primary and secondary glaucoma. It is important that clinicians are familiar with the presentation and management of peripapillary retinoschisis to understand its effects on the patient's glaucoma and to avoid unnecessary referral when the macula is not involved. PURPOSE: We present a case of peripapillary retinoschisis found incidentally on routine optical coherence tomographic (OCT) surveillance of primary open-angle glaucoma. CASE REPORT: A 70-year-old man presented for his annual diabetic eye examination. Surveillance with OCT revealed a splitting of the inner peripapillary retina corresponding to a previously noted notch in the right optic nerve. Further imaging of the right eye using enhanced depth imaging OCT revealed a defect in the lamina cribrosa that may have contributed to the formation and persistence of peripapillary retinoschisis. Retinal nerve fiber layer analysis showed a 5-year history of progressive temporal and inferotemporal thickening in the right eye. The patient was managed conservatively with instruction on regular Amsler grid testing. CONCLUSIONS: As seen in this case, peripapillary retinoschisis typically alters retinal nerve fiber layer thickness on OCT and can be mistakenly attributed to glaucomatous change. Glaucoma-associated peripapillary retinoschisis is usually not vision threatening and can be managed conservatively; in rare cases of progression to macular involvement, patients should be referred to a retina specialist. Permalink : https://bibliotheque.helb-prigogine.be/opac_css/index.php?lvl=notice_display&id= [article]Exemplaires
Cote Support Localisation Section Disponibilité aucun exemplaire Ocular Manifestation of Mantle Cell Lymphoma / Sara Hafeez in OVS : Optometry & Vision Science, vol. 99, 02 (février 2022)
[article]
in OVS : Optometry & Vision Science > vol. 99, 02 (février 2022)
Titre : Ocular Manifestation of Mantle Cell Lymphoma Type de document : article de périodique Auteurs : Sara Hafeez ; Alexis Mancini ; Joseph Mega ; Paul B. Greenberg ; Cory Siegel ; Amanda Hunter Année de publication : 2022 Langues : Français (fre) Descripteurs (mots clés) : [Thésaurus Mesh]Diagnostic
[Thésaurus Mesh]Lymphome à cellules du manteau
[Thésaurus Mesh]Maladies de l'oeil
[Thésaurus Mesh]ThérapeutiqueRésumé : SIGNIFICANCE
Mantle cell lymphoma (MCL) is a rare lymphoma that can present even more rarely in the orbit. Diagnosis, differentiation, and systemic treatment with the help of an oncologist are necessary for improved prognosis. Eye care providers must be vigilant when addressing ocular findings to determine next steps.
PURPOSE
We present a case of presumed orbital fat prolapse confirmed as MCL found on routine eye examination.
CASE REPORT
A 72-year-old White man presented for an annual comprehensive eye examination and was found to have conjunctival elevation in the superior and inferior fornices bilaterally. The patient had stable lymphadenopathy on positron emission tomography/computed tomography imaging 1 week before presentation. Coupled with the patient's recent diagnosis of systemic MCL, there was high suspicion that the conjunctival lesions were malignant. Biopsy of the conjunctival lesion confirmed MCL. A reevaluation of the previous imaging with a neuroradiologist confirmed the presence of orbital lesions consistent with MCL. The patient responded to treatment with low-dose focal radiation therapy.
CONCLUSIONS
Primary eye care providers should be aware of limitations of orbital imaging during routine positron emission tomography and computed tomography scans in those with MCL, and consultation with neuroradiology for image review may be useful if the clinical findings are suspicious.Permalink : https://bibliotheque.helb-prigogine.be/opac_css/index.php?lvl=notice_display&id= [article]Exemplaires
Cote Support Localisation Section Disponibilité aucun exemplaire