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1.
Arch. Soc. Esp. Oftalmol ; 97(11): 655-658, nov. 2022. ilus
Artigo em Espanhol | IBECS | ID: ibc-212047

RESUMO

Se presenta el caso de retinopatía autoinmune en un paciente con carcinoma microcítico de pulmón, no conocido hasta el momento, que se diagnosticó tras la exploración oftalmológica. La serología fue positiva para anticuerpos onconeuronales CV2/CRMP5. La retinopatía autoinmune es una entidad rara que puede pasarse por alto, y ser infradiagnosticada. Se produce por una reacción inmunomediada contra antígenos retinianos. La importancia de su diagnóstico precoz radica en que en muchos de los pacientes la sintomatología ocular aparece antes del diagnóstico del cáncer primario, por lo que su identificación y derivación precoz para estudio de extensión puede suponer el diagnóstico de una neoplasia primaria oculta hasta el momento. (AU)


We present a case of autoimmune retinopathy in a patient with unknown small cell lung cáncer (SCLC), which was diagnosed after ophthalmological examination. Serology was positive for CV2/CRMP5 onconeuronal antibodies. Autoimmune retinopathy is a rare entity that can be missed and underdiagnosed. It is produced by an immune-mediated reaction against retinal antigens. The importance of its early diagnosis lies in the fact that in many of the patients, ocular symptoms appear before the diagnosis of the primary cancer, so its early identification and referral for an extension study may lead to the diagnosis of a hidden primary neoplasm. (AU)


Assuntos
Humanos , Masculino , Idoso , Doenças Retinianas/imunologia , Autoanticorpos/imunologia , Carcinoma de Células Pequenas/diagnóstico , Carcinoma de Células Pequenas/imunologia , Neoplasias Pulmonares/diagnóstico , Neoplasias Pulmonares/imunologia , Detecção Precoce de Câncer , Angiofluoresceinografia
2.
Artigo em Inglês | MEDLINE | ID: mdl-36114140

RESUMO

We present a case of autoimmune retinopathy in a patient with unknown small cell lung cáncer (SCLC), which was diagnosed after ophthalmological examination. Serology was positive for CV2/CRMP5 onconeuronal antibodies. Autoimmune retinopathy is a rare entity that can be missed and underdiagnosed. It is produced by an immune-mediated reaction against retinal antigens. The importance of its early diagnosis lies in the fact that in many of the patients, ocular symptoms appear before the diagnosis of the primary cancer, so its early identification and referral for an extension study may lead to the diagnosis of a hidden primary neoplasm.

4.
Arch Soc Esp Oftalmol (Engl Ed) ; 96(11): 598-601, 2021 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-34756282

RESUMO

Ophthalmological diabetic complications are one of the main causes of blindness worldwide, so careful diagnostic and management is important. The screening plans implemented in our population made possible an early diagnosis and treatment, trying to reduce the consequences. Diabetic retinopathy is widely known, however we present the case of a rare retinal condition, acute panedothelial retinal leakage. It typically affects patients with type 1 DM and poor glycemic control. Its diagnosis is important since a strict metabolic control is sufficient for its resolution, avoiding aggressive therapies.


Assuntos
Diabetes Mellitus Tipo 1 , Retinopatia Diabética , Hiperglicemia , Cegueira , Diabetes Mellitus Tipo 1/complicações , Retinopatia Diabética/diagnóstico , Humanos , Retina
5.
J Fr Ophtalmol ; 44(10): 1536-1544, 2021 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-34728098

RESUMO

PURPOSE: To report the multimodal imaging in multiple evanescent white dot syndrome (MEWDS) during the acute and convalescent stages in order to better understand the focus of the inflammatory process. METHODS: Retrospective cohort study of 4 patients with MEWDS. Each patient underwent: enhanced depth imaging-optical coherence tomography (EDI-OCT), fundus autofluorescence (FAF), fluorescein angiography (FA), indocyanine green angiography (ICGA) and en-face OCT and OCT angiography (OCT-A). Choroidal subfoveal thickness (CST) was measured manually. All patients were studied in the acute stage and convalescent stage after disappearance of OCT abnormalities and resolution of visual symptoms. RESULTS: Four MEWDS patients with a mean age of 23.5years were studied (range: 16-33years). Two patients were women. Initial mean visual acuity (VA) was 80.25 ETDRS. Final mean VA was 84.25 ETDRS. OCT imaging showed disruption of the ellipsoid zone and a slightly elevated RPE layer with overlying hyperreflective material, all of which corresponded to hyperautofluorescent FAF lesions. FA revealed multiple hyperautofluorescent lesions, correlated with hypocyanescent spots on the late ICGA. OCT-A showed normal superficial and deep retinal capillary plexus as well as choriocapillaris. The disease was self-limited in all the cases, with a mean time of 9weeks to resolution (range: 4-16). CONCLUSION: The pathophysiology of MEWDS is still debated. We believe that there is still not enough evidence to implicate the outer retina as the primary cause. For now, we suggest that this transient disease is the consequence of choriocapillaris hypoperfusion, but further studies are required to elucidate this hypothesis.


Assuntos
Síndrome dos Pontos Brancos , Adulto , Feminino , Angiofluoresceinografia , Humanos , Imagem Multimodal , Estudos Retrospectivos , Tomografia de Coerência Óptica , Adulto Jovem
6.
Arch. Soc. Esp. Oftalmol ; 96(11): 598-601, nov. 2021. ilus
Artigo em Espanhol | IBECS | ID: ibc-218285

RESUMO

Las complicaciones oftalmológicas derivadas de la diabetes son una de las principales causas de ceguera en edad laboral a nivel mundial, por lo que es importante un manejo minucioso. Gracias a los planes de cribado implantados en nuestra población, es posible un diagnóstico y tratamiento precoz con el fin de disminuir las secuelas. La retinopatía diabética (RD) es una entidad conocida por todos nosotros, no obstante, presentamos el caso de una rara afectación retiniana, la capilaropatía edematosa aguda. Típicamente afecta a pacientes con diabetes mellitus tipo 1 (DM1) y mal control glucémico. Es importante su diagnóstico puesto que llevar un estricto control metabólico es suficiente para la resolución de la misma, evitando terapias agresivas (AU)


Ophthalmological diabetic complications are one of the main causes of blindness worldwide, so careful diagnostic and management is important. The screening plans implemented in our population made possible an early diagnosis and treatment, trying to reduce the consequences. Diabetic retinopathy is widely known, however we present the case of a rare retinal condition, acute panedothelial retinal leakage. It typically affects patients with diabetes mellitus (DM) type 1 and poor glycemic control. Its diagnosis is important since a strict metabolic control is sufficient for its resolution, avoiding aggressive therapies (AU)


Assuntos
Humanos , Feminino , Adolescente , Diabetes Mellitus Tipo 1/complicações , Retinopatia Diabética/diagnóstico , Edema , Doença Aguda
8.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-33298352

RESUMO

Ophthalmological diabetic complications are one of the main causes of blindness worldwide, so careful diagnostic and management is important. The screening plans implemented in our population made possible an early diagnosis and treatment, trying to reduce the consequences. Diabetic retinopathy is widely known, however we present the case of a rare retinal condition, acute panedothelial retinal leakage. It typically affects patients with diabetes mellitus (DM) type 1 and poor glycemic control. Its diagnosis is important since a strict metabolic control is sufficient for its resolution, avoiding aggressive therapies.

9.
Arch Soc Esp Oftalmol (Engl Ed) ; 95(11): 555-558, 2020 Nov.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-32593604

RESUMO

Pseudoxanthoma elasticum (PXE) is a rare genetic disorder characterised by elastic tissue alterations and caused by mutations in a single gene, ABCC6, on chromosome 16p that includes manifestations that are predominantly cutaneous, ocular and cardiovascular. PXE-like lesions in association with ß-thalassemia have previously been reported in the literature in patients with ß-thalassaemia intermediate and major, being clinically indistinguishable from classic PXE. The case is presented of a 10-year-old boy with ß-thalassaemia minor and characteristic lesions of PXE. It is worth noting the benefit of multimodal imaging in the diagnosis and monitoring of the lesions.

12.
Arch Soc Esp Oftalmol ; 79(12): 593-8, 2004 Dec.
Artigo em Espanhol | MEDLINE | ID: mdl-15627927

RESUMO

PURPOSE: Assess the efficacy of monoclonal antibody (daclizumab) therapy in the treatment of patients with non-infectious uveitis who do not respond to other immunosuppressive agents. MATERIAL AND METHOD: Ten patients with non-infectious intermediate and posterior uveitis were treated with intravenous daclizumab (humanized anti-IL-2 receptor monoclonal antibody) monthly for two years. RESULTS: 70% of the patients have had some improvement in their inflammatory activity being maintained without recurrence. 10% of the patients improved their visual acuity in two lines and the macular edema decreased. 20% of the patients continued to have recurrences, but not worse than the year before. 40% of the patients gave up having the treatment with corticosteroids and 30% with minimum dose (5 mg). No secondary effects were noted during the treatment. CONCLUSIONS: Daclizumab is effective and safe for long-term use in the treatment of uveitis which cannot be kept under control by other treatments. In time, it allows the dose of corticosteroids to be decreased or even discontinued.


Assuntos
Anticorpos Monoclonais/uso terapêutico , Imunoglobulina G/uso terapêutico , Imunossupressores/uso terapêutico , Uveíte/tratamento farmacológico , Adolescente , Adulto , Anticorpos Monoclonais Humanizados , Daclizumabe , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Recidiva
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