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1.
Bone Marrow Transplant ; 23(12): 1317-20, 1999 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-10414922

RESUMO

Varicella zoster virus (VZV) infection is a frequent complication following bone marrow transplantation (BMT). Involvement of the ophthalmic division of the trigeminal nerve, herpes zoster ophthalmicus (HZO), can result in significant and potentially vision-threatening ocular complications. We report the frequency and characteristics of HZO following BMT, including the timing of infection, treatment, ocular complications, and visual outcome. Between 1983 and 1997, 572 patients underwent BMT and seven children developed HZO at a median of 150 days following transplantation. All but one of the children had undergone allogeneic BMT. All of the children were treated with acyclovir after onset of the rash but none had received prophylactic therapy. All seven children developed ocular complications within the first 4 weeks following the onset of the dermatomal rash but none reported any symptoms during this period. Complications included keratitis in six, anterior uveitis in three and scleritis in one. Keratitis was an early complication developing within the first 4 weeks, while anterior uveitis and scleritis occurred later in the course of the disease. The high frequency of ocular complications and lack of symptoms in children with HZO following BMT suggests that early ophthalmologic evaluation is warranted in this group of patients. Prompt diagnosis and treatment of ocular complications is essential in the prevention of acute and long-term ocular sequelae in these children.


Assuntos
Transplante de Medula Óssea/efeitos adversos , Herpes Zoster Oftálmico/etiologia , Adolescente , Criança , Feminino , Humanos , Leucemia Mielogênica Crônica BCR-ABL Positiva/complicações , Leucemia Mielogênica Crônica BCR-ABL Positiva/terapia , Masculino , Leucemia-Linfoma Linfoblástico de Células Precursoras/complicações , Leucemia-Linfoma Linfoblástico de Células Precursoras/terapia
3.
Am J Ophthalmol ; 125(3): 292-300, 1998 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-9512145

RESUMO

PURPOSE: To report the observation that a transient vitreous inflammatory reaction may develop in the eyes of patients with acquired immunodeficiency syndrome (AIDS), cytomegalovirus retinitis, and an increased CD4+ T-lymphocyte count during treatment with antiretroviral therapy including a protease inhibitor. METHODS: We reviewed the medical records of eight patients with AIDS and cytomegalovirus retinitis who developed vitreous inflammatory reactions greater than those usually seen with this disease. RESULTS: Vitreous inflammatory reactions obscured the view of the posterior pole in all patients. No iris nodules, synechiae, glaucoma, or cystoid macular edema were observed. Six patients had unilateral cytomegalovirus retinitis, and, in each, the inflammation occurred only in the eye with cytomegalovirus retinitis. The vitreous inflammatory reactions were associated with clinically inactive cytomegalovirus retinitis in six patients, with disease reactivation in one patient, and were present at diagnosis of active disease in one patient. Cytomegalovirus retinitis has not recurred in any of these patients since their episodes of vitreous inflammation. Vitreous inflammation developed in all eight patients after a substantial increase in CD4+ T-lymphocyte counts caused by combination antiretroviral therapy. Five patients had CD4+ T-lymphocyte counts of greater than 100 cells per microl at the time the vitreous inflammatory reaction developed. No other causes of uveitis were found. CONCLUSIONS: Patients with AIDS and cytomegalovirus retinitis may develop transient intraocular inflammation associated with combination antiretroviral therapy. We believe that this inflammation reflects an improved immune response against cytomegalovirus.


Assuntos
Infecções Oportunistas Relacionadas com a AIDS/tratamento farmacológico , Fármacos Anti-HIV/efeitos adversos , Retinite por Citomegalovirus/tratamento farmacológico , Uveíte Posterior/induzido quimicamente , Corpo Vítreo/efeitos dos fármacos , Infecções Oportunistas Relacionadas com a AIDS/imunologia , Adulto , Fármacos Anti-HIV/uso terapêutico , Contagem de Linfócito CD4 , Linfócitos T CD4-Positivos/imunologia , Retinite por Citomegalovirus/imunologia , Quimioterapia Combinada , Oftalmopatias/induzido quimicamente , Feminino , Fundo de Olho , Humanos , Masculino , Recidiva
4.
Arch Ophthalmol ; 115(11): 1389-94, 1997 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-9366668

RESUMO

BACKGROUND: The ganciclovir implant is effective for the treatment of cytomegalovirus (CMV) retinitis. The device eventually runs out of drug, however, and must be replaced. We report our experience with exchanging ganciclovir implants during the course of a randomized clinical trial. METHODS: During our study, patients with newly diagnosed peripheral CMV retinitis were treated with a ganciclovir implant. The implant was scheduled for exchange at 32 weeks. It was exchanged earlier if progression of CMV retinitis occurred. Patient examinations and standard fundus photography were performed at 2-week intervals after the exchange procedure. RESULTS: Twenty-six exchange procedures were performed. Twenty-two eyes in 15 patients received a second implant and 4 eyes in 4 patients later received a third implant. Cytomegalovirus retinitis was rendered or maintained inactive in 22 of 23 cases with more than 1 month of follow-up after the second or third implants. Complications after the second implant procedure included transient vitreous hemorrhage in 5 eyes, postoperative inflammation in 1 eye, and retinal detachment in 1 eye. Median visual acuity returned to 20/25 by 28 days and to 20/20 by 42 days. Complications after the third implant procedure included dense vitreous hemorrhage in 3 of 4 eyes. Median survival time after a second implant procedure was 89 days. CONCLUSIONS: The initial ganciclovir implant exchange procedure is well tolerated with continued long-term control of CMV retinitis. Multiple reentries through the same wound may be associated with an increased risk for vitreous hemorrhage.


Assuntos
Antivirais/administração & dosagem , Retinite por Citomegalovirus/tratamento farmacológico , Ganciclovir/administração & dosagem , Complicações Pós-Operatórias , Antivirais/efeitos adversos , Retinite por Citomegalovirus/mortalidade , Retinite por Citomegalovirus/fisiopatologia , Implantes de Medicamento , Ganciclovir/efeitos adversos , Humanos , Procedimentos Cirúrgicos Oftalmológicos , Reoperação , Segurança , Taxa de Sobrevida , Fatores de Tempo , Acuidade Visual , Corpo Vítreo/efeitos dos fármacos
5.
Ophthalmology ; 103(9): 1512-6, 1996 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-8841315

RESUMO

BACKGROUND: Orbital metastasis from rhabdomyosarcoma is a rare disorder with a poor prognosis for long-term survival. Only one other detailed account of this disorder has appeared in the ophthalmic literature. METHODS: The authors report the clinical features of four patients with presumed orbital metastasis from alveolar and embryonal rhabdomyosarcoma. RESULTS: The most common ophthalmic manifestations of orbital metastasis from rhabdomyosarcoma in these patients included proptosis, reduced visual acuity, orbital pain, and motility disorders. Computed tomography documented orbital masses in all of the patients. In those patients with a primary tumor of the maxillary sinus, there was no evidence of direct extension into the orbit. Despite combination chemotherapy and radiation, all four patients died of their illness within 6 months of orbital metastasis. CONCLUSIONS: Although uncommon, rhabdomyosarcoma should be considered in the differential diagnosis of metastatic tumors to the orbit in children and adults. Despite the poor prognosis, prompt diagnosis and palliative radiotherapy may improve the quality of life for these patients with terminal disease.


Assuntos
Neoplasias do Seio Maxilar/patologia , Neoplasias Orbitárias/secundário , Neoplasias dos Seios Paranasais/patologia , Rabdomiossarcoma Alveolar/secundário , Rabdomiossarcoma Embrionário/secundário , Adolescente , Adulto , Pré-Escolar , Exoftalmia/etiologia , Evolução Fatal , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Transtornos da Motilidade Ocular/etiologia , Órbita/patologia , Dor/etiologia , Tomografia Computadorizada por Raios X , Transtornos da Visão/etiologia , Acuidade Visual
7.
Arch Ophthalmol ; 112(12): 1531-9, 1994 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-7993207

RESUMO

BACKGROUND AND METHODS: We performed a randomized controlled clinical trial to assess the safety and efficacy of a 1 microgram/h ganciclovir implant for the treatment of newly diagnosed cytomegalovirus (CMV) retinitis in patients with the acquired immunodeficiency syndrome (AIDS). Patients with previously untreated peripheral CMV retinitis were randomly assigned either to immediate treatment with the ganciclovir implant or to deferred treatment. Standardized fundus photographs were taken at 2-week intervals and analyzed in a masked fashion. The study end point was progression of retinitis based on the photographic assessment. RESULTS: Twenty-six patients (30 eyes) were enrolled. The median time to progression of retinitis was 15 days in the deferred treatment group (n = 16) vs 226 days in the immediate treatment group (n = 14) (P < .00001, log-rank test). During the study, 39 primary implants and 12 exchange implants were placed in immediate-treatment eyes, deferred-treatment eyes that progressed, or contralateral eyes that developed CMV retinitis. Postoperative complications in the total series included seven late retinal detachments and one retinal tear without detachment. Final visual acuity was 20/25 or better in 34 of 39 eyes. The estimated risk of developing CMV retinitis in the fellow eye was 50% at 6 months. Biopsy-proven visceral CMV disease developed in eight (31%) of 26 patients. The median survival was 295 days. CONCLUSION: The ganciclovir implant is effective for the treatment of CMV retinitis. Patients with unilateral CMV retinitis treated with the implant are likely to develop CMV retinitis in the fellow eye, and some patients will develop visceral CMV disease.


Assuntos
Infecções Oportunistas Relacionadas com a AIDS/tratamento farmacológico , Retinite por Citomegalovirus/tratamento farmacológico , Ganciclovir/uso terapêutico , Infecções Oportunistas Relacionadas com a AIDS/mortalidade , Adulto , Viés , Retinite por Citomegalovirus/mortalidade , Preparações de Ação Retardada , Progressão da Doença , Implantes de Medicamento/efeitos adversos , Feminino , Seguimentos , Ganciclovir/administração & dosagem , Humanos , Masculino , Pessoa de Meia-Idade , Perfurações Retinianas
8.
Ophthalmic Surg ; 21(6): 413-5, 1990 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-2381676

RESUMO

We present a case of pupillary block glaucoma that developed after cataract extraction in a pediatric patient. To prevent pupillary block and secondary glaucoma after cataract surgery we recommend that all pediatric cataract patients be given a prophylactic peripheral iridectomy.


Assuntos
Extração de Catarata/efeitos adversos , Glaucoma/etiologia , Criança , Feminino , Glaucoma/prevenção & controle , Humanos , Pressão Intraocular , Iris/cirurgia , Terapia a Laser , Acuidade Visual
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