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1.
Ophthalmol Retina ; 5(8): 824-830, 2021 08.
Artigo em Inglês | MEDLINE | ID: mdl-33221516

RESUMO

PURPOSE: To evaluate the effect of adding topotecan to melphalan for the treatment of retinoblastoma using intra-arterial chemotherapy (IAC). DESIGN: Single-center, consecutive case series. PARTICIPANTS: All eyes treated with IAC at the University of Siena, Siena, Italy, from 2008 to 2019. METHODS: Eyes were treated via IAC with either melphalan monotherapy or melphalan plus topotecan. The characteristics and outcomes of these 2 groups were compared. MAIN OUTCOME MEASURES: The main outcome measure was globe salvage rate. Additionally, a complete summary of all adverse events for all eyes was compared between groups and included local, regional, and systemic events causing both transient and permanent effects. RESULTS: A total of 193 patients and 208 eyes were treated with IAC between April 2008 and October 2019. Melphalan alone (MA) was used to treat 44 patients and 50 eyes for a total of 191 procedures. The combination of melphalan plus topotecan (MPT) was used to treat 149 patients and 158 eyes for a total of 780 procedures. Groups were similar in terms of age at presentation. The MPT group included more advanced eyes (P < 0.001) and had shorter follow-up time (mean 47 vs. 120 months in the MA group, P < 0.001). The MPT group required less laser and cryotherapy after treatment (32% of eyes vs. 50% of eyes in the MA group, P < 0.001); there was no other difference in the number of adjuvant treatments required between groups. There was no difference in the number of acute adverse events, both systemic and local, between groups. There was no difference in the number of transient or permanent intraocular side effects between groups. Kaplan-Meier survival analysis estimated a better globe salvage rate in the MPT group (66%) compared with the MA group (58%, P = 0.05). CONCLUSIONS: In this case series, the addition of topotecan to melphalan did not alter the IAC side effect profile and may contribute to improved globe salvage.


Assuntos
Melfalan/administração & dosagem , Retina/diagnóstico por imagem , Neoplasias da Retina/tratamento farmacológico , Retinoblastoma/tratamento farmacológico , Topotecan/administração & dosagem , Antineoplásicos Alquilantes/administração & dosagem , Pré-Escolar , Relação Dose-Resposta a Droga , Quimioterapia Combinada , Feminino , Angiofluoresceinografia , Seguimentos , Fundo de Olho , Humanos , Lactente , Injeções Intra-Arteriais , Masculino , Estudos Prospectivos , Neoplasias da Retina/diagnóstico , Retinoblastoma/diagnóstico , Inibidores da Topoisomerase I/administração & dosagem , Resultado do Tratamento
2.
Open Ophthalmol J ; 10: 27-32, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27014384

RESUMO

PURPOSE: To present the case of an 18 month old boy with Coats' disease who was found to have anterior chamber cholesterolosis. METHODS: Case presentation and review of reported cases. RESULTS: An 18 month old boy presented with unilateral stage 3B Coats' disease without other clinical findings. Two weeks after presentation he returned with xanthocoria due to anterior chamber cholesterolosis. He subsequently developed hyphema, neovascular glaucoma, and was enucleated. His case is compared to all previously reported cases of Coats' disease leading to anterior chamber cholesterolosis. CONCLUSION: The presentation of anterior chamber cholesterolosis in Coats' disease can range from the incidental finding in an asymptomatic patient to acute angle closure glaucoma with pain and acutely decreased vision. Clinicians should be aware of this potential complication of Coats' disease as it denotes a poor visual prognosis.

3.
J AAPOS ; 19(5): 474-8, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26486036

RESUMO

Cornelia de Lange syndrome (CdLS) can result in multiple congenital abnormalities and numerous ocular findings. We report the case of a 6-year-old boy with history of CdLS who presented with Coats disease. The findings in this case are compared to those found in the two previously reported cases of concomitant CdLS and Coats disease. The low incidence of these two disorders makes it highly unlikely that the connection is random in these 3 cases. The number of patients with both Cornelia de Lange syndrome and Coats disease is likely underestimated due to the difficulty in examining the peripheral retina in this patient population.


Assuntos
Síndrome de Cornélia de Lange/complicações , Descolamento Retiniano/etiologia , Telangiectasia Retiniana/etiologia , Inibidores da Angiogênese/uso terapêutico , Bevacizumab/uso terapêutico , Criança , Síndrome de Cornélia de Lange/diagnóstico , Síndrome de Cornélia de Lange/tratamento farmacológico , Exsudatos e Transudatos , Humanos , Injeções Intravítreas , Masculino , Descolamento Retiniano/diagnóstico por imagem , Descolamento Retiniano/tratamento farmacológico , Telangiectasia Retiniana/diagnóstico , Telangiectasia Retiniana/tratamento farmacológico , Ultrassonografia , Fator A de Crescimento do Endotélio Vascular/antagonistas & inibidores , Acuidade Visual/efeitos dos fármacos
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