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7.
Br J Ophthalmol ; 101(4): 401-405, 2017 04.
Artigo em Inglês | MEDLINE | ID: mdl-27872047

RESUMO

OBJECTIVE: To compare two methods for diagnosing mild papilloedema (PO) using peripapillary total retinal (PTR) and retinal nerve fibre layer (RNFL) thickness measurement by spectral domain optical coherence tomography (OCT) in patients suffering from posterior uveitis. METHODS: 17 eyes in 17 patients with PO caused by posterior uveitis, 15 eyes in 15 patients with uveitis but with no PO based on slit lamp analysis were studied. High-quality OCT fundus images were analysed and graded by three masked observers using the Modified Frisén Scale. Eyes with PO were divided into two subgroups: mild (n=15) and moderate-severe PO (n=2). Two measurement methods were evaluated and compared: RNFL and PTR thickness measurements centred on the optic disc. Thickness values were calculated overall and for each quadrant and compared between groups. The main outcome measures were RNFL and PTR thickness, and thickness variation between control and affected patients for both protocols. RESULTS: Average RNFL and PTR thickness in the moderate-severe PO, mild PO and control groups were 274.5±54.45 µm, 134±31.69 µm, 97.4±14.43 µm and 722.25±29.34 µm, 437.53±84.47 µm, 327.8±25.92 µm, respectively. Mild PO differed from the control groups according to both the RNLF (p=0.0006) and the PTR (p=0.0002) measurements. The average thickness variation between control and mild PO was significantly different between RNFL and PTR measurements: 36.6 µm vs 109.73 µm (p<0.0001), respectively. CONCLUSIONS: PTR thickness measurement increases the sensitivity of detection of mild PO and could be useful for diagnosing and monitoring papillitis. A new protocol should be developed to measure PTR in the same 3.5 mm disc as the RNFL measurement.


Assuntos
Fibras Nervosas/patologia , Papiledema/patologia , Retina/patologia , Tomografia de Coerência Óptica , Uveíte Posterior/patologia , Adolescente , Adulto , Criança , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Papiledema/diagnóstico por imagem , Papiledema/etiologia , Reprodutibilidade dos Testes , Retina/diagnóstico por imagem , Células Ganglionares da Retina , Uveíte Posterior/complicações , Uveíte Posterior/diagnóstico por imagem , Uveíte Posterior/fisiopatologia
11.
J Fr Ophtalmol ; 36(4): 362-7, 2013 Apr.
Artigo em Francês | MEDLINE | ID: mdl-23318000

RESUMO

INTRODUCTION: Intravitreal implantation of Ozurdex(®) (Allergan Inc., Irvine, CA, USA) is being used widely for the treatment of macular edema secondary to retinal vein occlusion and in the setting of non-infectious posterior uveitis. We describe a complication little reported in the literature until now: migration of the dexamethasone implant into the anterior chamber. PATIENTS AND METHODS: We report three cases of migration in two pseudophakic patients with iris claw lenses (on the anterior and posterior aspects of the iris) and in one pseudophakic patient with a posterior chamber IOL and zonular rupture. DISCUSSION: The risk of anterior chamber migration of the Ozurdex(®) implant is increased in cases of prior vitrectomy (three cases), prone positioning and dilation of the pupil (mydriasis). Clinical tolerability of the implant in the anterior chamber is poor in all cases, with diffuse corneal edema. Endothelial cell loss occurs, as demonstrated by specular microscopy performed in two of our patients. Removal or repositioning of the Ozurdex(®) implant into the posterior segment must be performed without delay because of the risk of endothelial toxicity. CONCLUSION: Patients without perfect zonular/posterior capsular integrity present a high risk of anterior chamber migration of the Ozurdex(®) implant. In such cases, anti-VEGF therapies should be discussed as an alternative.


Assuntos
Câmara Anterior/patologia , Migração do Implante de Lente Intraocular/diagnóstico , Dexametasona/administração & dosagem , Implantes de Medicamento , Falha de Prótese , Pseudofacia , Idoso , Migração do Implante de Lente Intraocular/complicações , Migração do Implante de Lente Intraocular/cirurgia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Falha de Prótese/efeitos adversos , Pseudofacia/complicações , Pseudofacia/diagnóstico , Pseudofacia/cirurgia , Corpo Vítreo
12.
J Fr Ophtalmol ; 36(4): 368-71, 2013 Apr.
Artigo em Francês | MEDLINE | ID: mdl-23261208

RESUMO

Iridoschisis is a rare degenerative disease characterized by the separation of the anterior iris stroma from the posterior layer. The anterior layer splits into strands, and the free ends float freely in the anterior chamber. We report the case of a 57-year-old man, in whom we incidentally discovered isolated unilateral iris atrophy. The patient had no history of the common causes of atrophy (herpes, pigment dispersion, ocular trauma, etc.). During follow-up, the atrophy gradually worsened, with an increase in the number and bilaterality of the lesions. Ultrasound biomicroscopy (UBM) and optical coherence tomography (OCT) of anterior chamber showed thinning of the anterior iris and cleavage of the iris into two layers, an imaging result which, to our knowledge, has not yet been reported in the literature. Familiarity with iridoschisis is important, due to its frequent association with glaucoma, so that appropriate screening can be carried out at the time of diagnosis and on follow-up.


Assuntos
Doenças da Íris/diagnóstico , Iris/patologia , Câmara Anterior/diagnóstico por imagem , Câmara Anterior/patologia , Atrofia/diagnóstico , Atrofia/diagnóstico por imagem , Humanos , Iris/diagnóstico por imagem , Doenças da Íris/diagnóstico por imagem , Doenças da Íris/patologia , Masculino , Microscopia Acústica , Pessoa de Meia-Idade , Radiografia , Tomografia de Coerência Óptica
13.
Cesk Slov Oftalmol ; 69(3): 134-7, 2013 Aug.
Artigo em Tcheco | MEDLINE | ID: mdl-24437961

RESUMO

PURPOSE: To present data pointing out that small tumour size might not be a sufficient predictor of good prognosis of choroidal melanoma and present a new promising therapy of hepatic metastasis. METHODS: Retrospective, noncomparative case report of two patients with small choroidal melanoma. RESULTS: Two cases of small choroidal melanoma which developed metastases are described. Both patients underwent radiotherapy of the primary tumour. Metastases were treated by combined therapy in patient 1 while in patient 2 a new therapeutic modality of stereotactic radiotherapy, Cyberknife, was applied. Patient 1 died from metastatic spread 7,6 years after primary therapy despite a very good local tumour control. Patient 2 died 11,3 years after primary therapy due to intercurrent disease with a very good local eye findings and hepatic metastasis in regression. CONCLUSION: Choroidal melanoma of a small size can develop into metastatic disease even long time after satisfactory primary treatment. Further studies are required to assess the risk factors of metastatic spread in small uveal melanomas. Cyberknife stereotactic radiotherapy seems to be a promising therapeutic method of a solitary hepatic metastasis. Key words: choroidal melanoma, metastasis, prognostic factors, stereotactic radiotherapy.


Assuntos
Neoplasias da Coroide/secundário , Melanoma/secundário , Radiocirurgia/métodos , Neoplasias Uveais/secundário , Adulto , Neoplasias da Coroide/diagnóstico , Neoplasias da Coroide/cirurgia , Diagnóstico Diferencial , Evolução Fatal , Seguimentos , Humanos , Masculino , Melanoma/diagnóstico , Melanoma/cirurgia , Metástase Neoplásica , Neoplasias Uveais/diagnóstico , Neoplasias Uveais/cirurgia
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