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[PMID]:29400026
[Au] Autor:El Bakkouri W; Blanc R; Benzakin S; Abdellaoui A; Boyeldieu L; Ayache D
[Ti] Título:[Innovations in interventional radiology applied to the field of otolaryngology: A pictorial essay].
[So] Source:Rev Laryngol Otol Rhinol (Bord);136(3):91-5, 2015.
[Is] ISSN:0035-1334
[Cp] País de publicação:France
[La] Idioma:fre
[Ab] Resumo:The management of hypervascular ENT tumors is usually complex and requires a multidisciplinary approach because of the risk of serious intra-operative bleeding and of potential injuries to cranial nerves and/or large cervical vessels. Over the last four decades, advances in neuro-interventional radio­logical procedures have produced a range of adjunctive endo­vascular techniques in addition to conventional surgery. A pictorial essay in ENT specialty is presented in this article highlighting the most relevant innovations in interventional radiology.
[Mh] Termos MeSH primário: Otolaringologia
Radiologia Intervencionista
[Mh] Termos MeSH secundário: Hemorragia/terapia
Seres Humanos
Artéria Oftálmica
Neoplasias da Retina/tratamento farmacológico
Retinoblastoma/tratamento farmacológico
Zumbido/terapia
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1803
[Cu] Atualização por classe:180308
[Lr] Data última revisão:
180308
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:180206
[St] Status:MEDLINE


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[PMID]:29443780
[Au] Autor:Lyu S; Zhang M; Wang RK; Gao Y; Zhang Q; Min X
[Ad] Endereço:Department of Ophthalmology, West China Hospital of Sichuan University, Wuhou District, Chengdu, Sichuan, China.
[Ti] Título:Analysis of the characteristics of optical coherence tomography angiography for retinal cavernous hemangioma: A case report.
[So] Source:Medicine (Baltimore);97(7):e9940, 2018 Feb.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:RATIONALE: Retinal cavernous hemangioma is a rare congenital vascular malformation with typical fundus changes. Optical coherence tomography angiography (OCTA), which is in rise in the recent years, is a rapid and noninvasive technology to assist in obtaining information regarding the blood flow changes in the fundus lesions from different layers without injecting a contrast agent. PATIENT CONCERNS: A 40-year-old male patient with visual occlusion in the right eye for >1 month was reported. DIAGNOSES: Retinal cavernous hemangioma was diagnosed by fundus examination, fluorescein angiography (FA) and OCTA, and the characteristics of OCTA images were analyzed. INTERVENTIONS: The lesion occurred outside the macula, the central vision remained basically normal, and no significant complications were noted in this patient. Therefore, we preferred to regularly follow-up without therapeutic intervention. CONCLUSIONS: OCTA can display fundus blood flow and vascular lesions noninvasively and rapidly. On OCTA, retinal cavernous hemangiomas showed characteristic changes and have good correspondence with fundus imaging and FA examinations. Moreover, OCTA remains more sensitive to vascular abnormalities, and imaging remains clearer, providing new diagnosis and follow-up route for this disease.
[Mh] Termos MeSH primário: Angiofluoresceinografia
Hemangioma Cavernoso/diagnóstico por imagem
Neoplasias da Retina/diagnóstico por imagem
Vasos Retinianos/diagnóstico por imagem
Tomografia de Coerência Óptica
[Mh] Termos MeSH secundário: Adulto
Seres Humanos
Masculino
Fluxo Sanguíneo Regional
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180220
[Lr] Data última revisão:
180220
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:180215
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000009940


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[PMID]:29212524
[Au] Autor:Essadi I; Lalya I; Kriet M; El Omrani A; Belbaraka R; Khouchani M
[Ad] Endereço:Medical Oncology, Ibn Sina Military Hospital, Cadi Ayad University, Marrakesh, Morocco. ismail_onco@yahoo.fr.
[Ti] Título:Successful management of retinal metastasis from renal cancer with everolimus in a monophthalmic patient: a case report.
[So] Source:J Med Case Rep;11(1):340, 2017 Dec 07.
[Is] ISSN:1752-1947
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: The retina is an uncommon site for metastases, in particular from solid tumors. Some authors have reported a recent increase in the incidence of metastases in infrequent sites, such as brain or bone, probably due to the expanded treatment options and the resulting improved survival. Choroidal metastasis is the most common type of intraocular malignancy. The most common primary sites associated with choroidal metastasis are breast cancer in women and lung cancer in men. Treatment options are limited, but they must be discussed and adapted to the patient profile. CASES PRESENTATION: We report a case of a 62-year-old Moroccan man with a history of monophthalmitis secondary to a war injury of 30 years' duration. He has been followed for 28 months for metastatic clear-cell renal carcinoma. The first-line treatment was effective for 24 months, before disease progression as retinal metastasis and accentuation of lung metastases. A second-line treatment with everolimus resulted in marked improvement of symptoms, complete recovery of visual function, and partial response in retinal localization. CONCLUSIONS: Choroidal metastasis of renal cancer is a rare situation that must be actively sought in order to arrive at a suitable therapeutic approach.
[Mh] Termos MeSH primário: Antineoplásicos/uso terapêutico
Carcinoma de Células Renais/tratamento farmacológico
Everolimo/uso terapêutico
Traumatismos Oculares
Neoplasias Renais/patologia
Neoplasias da Retina/tratamento farmacológico
Lesões Relacionadas à Guerra
[Mh] Termos MeSH secundário: Carcinoma de Células Renais/secundário
Progressão da Doença
Seres Humanos
Neoplasias Pulmonares/diagnóstico por imagem
Neoplasias Pulmonares/secundário
Masculino
Meia-Idade
Neoplasias da Retina/diagnóstico por imagem
Neoplasias da Retina/secundário
Tomografia Computadorizada por Raios X
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Antineoplastic Agents); 9HW64Q8G6G (Everolimus)
[Em] Mês de entrada:1801
[Cu] Atualização por classe:180130
[Lr] Data última revisão:
180130
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171208
[St] Status:MEDLINE
[do] DOI:10.1186/s13256-017-1501-2


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[PMID]:29246122
[Au] Autor:Said AMA; Elbayomi AM; Shaat AAK
[Ad] Endereço:Ophthalmology Department, Faculty of Medicine, Ain Shams University, Corresponding author address: 10 th Fawzy Elmoteay street, Heliopolis, Cairo, Postal code: 11736, Egypt. dr_azza_22@hotmail.com.
[Ti] Título:Structural changes of the macula and optic nerve head in the remaining eyes after enucleation for retinoblastoma: an optical coherence tomography study.
[So] Source:BMC Ophthalmol;17(1):251, 2017 Dec 16.
[Is] ISSN:1471-2415
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: To describe objectively the possible structural changes of the macula and optic nerve head in the free eyes of unilateral cured retinoblastoma patients and, also after enucleation using spectral domain optical coherence tomography. METHODS: A cross sectional study involving 60 patients subdivided into three groups; 15 unilateral RB patients in whom enucleation was indicated as a sole treatment performed earlier in life [(study group (I)], 15 unilateral RB patients who had completely regressed disease with a preserved eye [(study group (II)] and 30 age and sex matched healthy controls. The remaining and free eyes in study groups and right eyes of control group had full ophthalmological examination, static automated perimetry and optical coherence tomography of the macula and optic nerve head. RESULTS: In study group (II); a significant thinning of total macula, central fovea, ganglion cell layer (GCL), ganglion cell complex (GCC), and some sectors of outer nuclear layer (P- values ≤0.05) was found with no significant difference in peripapillary nerve fiber layer (pRNFL) thickness and optic nerve head parameters compared to the control group and the study group (I). A significantly thickened total macula, GCL, GCC, and pRNFL in study group (I) compared to study group (II). Thickened pRNFL was significantly correlated to standard automated perimetry pattern deviations. No significant difference was found between study group (I) and control group. CONCLUSION: Retinoblastoma eyes characterized by thinning of central fovea, GCL, GCC compared to the control group. After unilateral enucleation, increased GCC and pRNFL thicknesses were detected compared to retinoblastoma group.
[Mh] Termos MeSH primário: Enucleação Ocular
Macula Lutea/patologia
Disco Óptico/patologia
Neoplasias da Retina/patologia
Retinoblastoma/patologia
[Mh] Termos MeSH secundário: Adolescente
Adulto
Estudos de Casos e Controles
Criança
Pré-Escolar
Estudos Transversais
Feminino
Seres Humanos
Masculino
Fibras Nervosas/patologia
Células Ganglionares da Retina/patologia
Neoplasias da Retina/cirurgia
Retinoblastoma/cirurgia
Tomografia de Coerência Óptica/métodos
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1801
[Cu] Atualização por classe:180105
[Lr] Data última revisão:
180105
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171217
[St] Status:MEDLINE
[do] DOI:10.1186/s12886-017-0650-9


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[PMID]:29217028
[Au] Autor:Andreoli MT; Chau FY; Shapiro MJ; Leiderman YI
[Ad] Endereço:Illinois Eye and Ear Infirmary, UIC Department of Ophthalmology and Visual Sciences, University of Illinois, Chicago, IL.. Electronic address: michaelandreoli@gmail.com.
[Ti] Título:Epidemiological trends in 1452 cases of retinoblastoma from the Surveillance, Epidemiology, and End Results (SEER) registry.
[So] Source:Can J Ophthalmol;52(6):592-598, 2017 Dec.
[Is] ISSN:1715-3360
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:OBJECTIVE: To assess retinoblastoma epidemiological trends in the Surveillance, Epidemiology, and End Results (SEER) registry. METHODS: All cases of retinoblastoma in the SEER database from 1973 to 2009 were identified. Kaplan-Meier survival analyses were performed for pathological grade, patient age, sex, year of diagnosis, and treatment modality. Cox proportional hazards regression assessed the impact of patient and tumour characteristics on survival. RESULTS: 1452 cases of retinoblastoma were analyzed. The mean patient age at diagnosis was 1.44 years. The tumour was unilateral in 71.0% and bilateral in 29.0%. The mean follow-up was 129.1 months. Overall survival increased during the study interval. Patients with bilateral tumours were diagnosed at an earlier age (0.46 years) than patients with unilateral disease (1.77 years; p < 0.0001). Bilateral retinoblastoma (90.3% 10-year overall survival) was associated with decreased overall survival than unilateral retinoblastoma (96.1% 10-year overall survival). Bilateral retinoblastoma was also associated with an increased incidence of nonocular malignancies (7.8%) compared with unilateral retinoblastoma (1.3%; p < 0.0001). Grade 1 tumours were diagnosed at a younger age (0.94 years) than grade 3 (2.24 years) and grade 4 tumours (2.14 years; p < 0.0001). Lower grade and lower stage tumours were independently associated with increased survival. In multivariate Cox proportional hazards analysis, T stage and laterality were the only covariates that correlated with overall survival. CONCLUSIONS: There appear to be associations between retinoblastoma tumour features such as tumour stage, pathological grade, and laterality with patient characteristics such as age at diagnosis, overall survival, and second malignancies.
[Mh] Termos MeSH primário: Sistema de Registros
Neoplasias da Retina/epidemiologia
Retinoblastoma/epidemiologia
Programa de SEER/estatística & dados numéricos
[Mh] Termos MeSH secundário: Adolescente
Adulto
Criança
Pré-Escolar
Bases de Dados Factuais
Estudos Epidemiológicos
Feminino
Seres Humanos
Incidência
Lactente
Estimativa de Kaplan-Meier
Masculino
Estadiamento de Neoplasias
Neoplasias da Retina/patologia
Neoplasias da Retina/radioterapia
Retinoblastoma/patologia
Retinoblastoma/radioterapia
Taxa de Sobrevida
Estados Unidos/epidemiologia
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1712
[Cu] Atualização por classe:171226
[Lr] Data última revisão:
171226
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171209
[St] Status:MEDLINE


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[PMID]:29230267
[Au] Autor:Shifa JZ; Gezmu AM
[Ad] Endereço:Department of Surgery, Faculty of Medicine, University of Botswana, Gaborone, Botswana.
[Ti] Título:Presenting signs of retinoblastoma at a tertiary level teaching hospital in Ethiopia.
[So] Source:Pan Afr Med J;28:66, 2017.
[Is] ISSN:1937-8688
[Cp] País de publicação:Uganda
[La] Idioma:eng
[Ab] Resumo:Introduction: Retinoblastoma is a primary malignant intraocular neoplasm that arise from immature retinoblasts with in developing retina. The commonest presenting sign in developing country is proptosis which is the late presenting sign. We report presenting signs of retinoblastoma in Ethiopian children seen at a tertiary level teaching hospitals in Ethiopia. Methods: Prospective case series study was done on children who presented with retinoblastoma between May 1, 2005 and September 1, 2006. This study was done as part of requirement for partial fulfilment of certificate of specialty study in ophthalmology during the year 2005 to 2006. SPSS 11 statistical package was used to analyse the data. Results: Among 41 patients seen during the study period, 24 (58.5%) were males and 17(41%) were females. Unilateral retinoblastoma was found in 32 (78%) patients and bilateral cases were found in 9(22%). Mean age of onset for right eye was 27.5 months and left eye 33.7 months. The mean ages of presentation at time of diagnosis for right and left eye were 34.4 and 40.2 months, respectively .In bilateral retinoblastoma mean age of presentation was 33.3 months. The commonest presenting sign was proptosis 22(53.7%) followed by leucocorea nine (22%),ocular inflammation four (9.0 %), strabismus three (7.3%), glaucoma one (2.4%), loss of vision one (2.4%)and hyphemaone (2.4%). Conclusion: The commonest presenting signs of retinoblastoma in our set up were Proptosis followed by leucocorea. This is due to late presentation of patient and late referral by medical professionals. Health education to the public and health professionals will help early detection of retinoblastoma.
[Mh] Termos MeSH primário: Exoftalmia/etiologia
Neoplasias da Retina/diagnóstico
Retinoblastoma/diagnóstico
[Mh] Termos MeSH secundário: Idade de Início
Pré-Escolar
Detecção Precoce de Câncer
Etiópia
Exoftalmia/epidemiologia
Feminino
Hospitais de Ensino
Seres Humanos
Masculino
Estudos Prospectivos
Encaminhamento e Consulta
Neoplasias da Retina/epidemiologia
Neoplasias da Retina/patologia
Retinoblastoma/epidemiologia
Retinoblastoma/patologia
Estrabismo/epidemiologia
Estrabismo/etiologia
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1712
[Cu] Atualização por classe:171222
[Lr] Data última revisão:
171222
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171213
[St] Status:MEDLINE
[do] DOI:10.11604/pamj.2017.28.66.11199


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[PMID]:29197363
[Au] Autor:Wang P; Li YJ; Zhang SB; Cheng QL; Zhang Q; He LS
[Ad] Endereço:Department of Ophthalmology, Tangdu Hospital of Fourth Military Medical University, Xi'an, Shaanxi, China.
[Ti] Título:Metastatic retinoblastoma of the parotid and submandibular glands: a rare case report.
[So] Source:BMC Ophthalmol;17(1):229, 2017 Dec 02.
[Is] ISSN:1471-2415
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Retinoblastoma is the most common intraocular malignancy occurring in children. It can metastasize to the regional lymph nodes, central nervous system and distant organs usually the bones and bone marrow and very rarely to the soft tissue. Here, we report a case of unilateral retinoblastoma in a 4-year-old girl accompanied by a large metastasis of the parotid and submandibular glands that developed about 6 months previously and gradually increased in size 5 months after enucleation of the left eye. CASE PRESENTATION: A 4-year-old girl with a history of unilateral retinoblastoma presented with a large, painful and worsening mass (about 20 × 23 cm) of the left side of the neck. Following surgery, the orbital tumour was completely resected, and the large tumour invasion range in the left side of the neck was not resected completely. Histopathological examination revealed retinoblastoma of the orbit and the parotid and submandibular glands. After chemotherapy and additional local radiotherapy on the parotid and submandibular glands, the tumour was inactive and stable. CONCLUSIONS: Delayed detection and inappropriate management contribute to poor outcomes. Fundus examinations, education regarding the early signs of RB, and optimization of the therapeutic strategy for RB may play important roles in ocular health.
[Mh] Termos MeSH primário: Neoplasias Mandibulares/secundário
Neoplasias Orbitárias/patologia
Neoplasias Parotídeas/secundário
Neoplasias da Retina/patologia
Retinoblastoma/patologia
[Mh] Termos MeSH secundário: Pré-Escolar
Feminino
Seres Humanos
Glândula Submandibular/patologia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1712
[Cu] Atualização por classe:171220
[Lr] Data última revisão:
171220
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171204
[St] Status:MEDLINE
[do] DOI:10.1186/s12886-017-0627-8


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[PMID]:28903151
[Au] Autor:Sreelakshmi KV; Chandra A; Krishnakumar S; Natarajan V; Khetan V
[Ad] Endereço:Shri Bhagawan Mahavir Vitreoretinal Services, Sankara Nethralaya, Chennai, India.
[Ti] Título:Anterior Chamber Invasion in Retinoblastoma: Not an Indication for Adjuvant Chemotherapy.
[So] Source:Invest Ophthalmol Vis Sci;58(11):4654-4661, 2017 Sep 01.
[Is] ISSN:1552-5783
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Purpose: In retinoblastoma, adjuvant chemotherapy after enucleation is given in eyes with histopathological high-risk features (HRFs) to reduced mortality. Anterior chamber seeds (AC seeds) on histopathological evaluation are a contentious finding. This study attempts to determine the effect of AC seeds on the survival rate. Methods: This is a retrospective case record review. Eyes were divided into four groups: those with neither AC seeds nor HRFs, those with only HRFs, those with only AC seeds, and those with both HRFs and AC seeds. The groups were compared for demographic and clinical features and survival curves were plotted for each. Results: For the 212 eyes included in the study, mean age was 30.5 ± 36.8 months. Children with only AC seeds were significantly older (75.3 ± 94.6 months) (P = 0.004). Chemotherapy was administered in 81 (38.2%) of 212 eyes; 16 (13.7%) of 117 eyes without HRF and in 65 (68.4%) of 95 eyes with HRFs (P < 0.001). The survival rate at 1, 3, and 5 years was the highest for the group with only AC seeds, although the difference was not statistically significant. Conclusions: We conclude that AC seeds do not, by themselves, constitute an independent risk factor for metastasis. These children need not be treated with immediate adjuvant chemotherapy, but, instead, can be followed with regular screening for metastasis. However, AC seeds are seen in only a small proportion of enucleated eyes. A larger study would better validate our study results.
[Mh] Termos MeSH primário: Câmara Anterior/patologia
Inoculação de Neoplasia
Neoplasias da Retina/patologia
Retinoblastoma/patologia
[Mh] Termos MeSH secundário: Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico
Carboplatina/uso terapêutico
Quimioterapia Adjuvante
Criança
Pré-Escolar
Etoposídeo/uso terapêutico
Enucleação Ocular
Feminino
Seres Humanos
Lactente
Masculino
Invasividade Neoplásica
Neoplasias da Retina/tratamento farmacológico
Neoplasias da Retina/mortalidade
Retinoblastoma/tratamento farmacológico
Retinoblastoma/mortalidade
Estudos Retrospectivos
Fatores de Risco
Taxa de Sobrevida
Vincristina/uso terapêutico
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
5J49Q6B70F (Vincristine); 6PLQ3CP4P3 (Etoposide); BG3F62OND5 (Carboplatin)
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170922
[Lr] Data última revisão:
170922
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170914
[St] Status:MEDLINE
[do] DOI:10.1167/iovs.17-22111


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[PMID]:28810047
[Au] Autor:Pierro L; Marchese A; Gagliardi M; Bandello F
[Ti] Título:Optical Coherence Tomography Angiography of Retinal Cavernous Hemangioma.
[So] Source:Ophthalmic Surg Lasers Imaging Retina;48(8):684-685, 2017 Aug 01.
[Is] ISSN:2325-8179
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Retinal cavernous hemangioma is a rare, benign, retinal tumor characterized by angiomatous proliferation of vessels within the inner retina or the optic disc.1 Here we report a case of retinal cavernous hemangioma on the margin of the optic disc in the right eye of a 61-year-old asymptomatic female. The lesion was studied with multimodal imaging which included structural optical coherence tomography, fluorescein angiography, blue fundus auto-fluorescence, optical coherence tomography angiography (OCTA) (DRI OCT Triton; Topcon, Tokyo, Japan) and visual field examination. Blood circulation inside retinal cavernous hemangioma lesion is typically low-stagnant.2 However, OCTA demonstrated blood flow inside the lesion, illustrating its vascular circulation.3 Visual field was within the normal limits, except from a slight enlargement of the blind spot. [Ophthalmic Surg Lasers Imaging Retina. 2017;48:684-685.].
[Mh] Termos MeSH primário: Angiofluoresceinografia/métodos
Hemangioma Cavernoso/diagnóstico
Retina/patologia
Neoplasias da Retina/diagnóstico
Tomografia de Coerência Óptica/métodos
[Mh] Termos MeSH secundário: Diagnóstico Diferencial
Feminino
Fundo de Olho
Seres Humanos
Meia-Idade
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170929
[Lr] Data última revisão:
170929
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170816
[St] Status:MEDLINE
[do] DOI:10.3928/23258160-20170802-14


  10 / 2749 MEDLINE  
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[PMID]:28728187
[Au] Autor:Thirumalesh MB; Jain A; Agrawal S; Bhujang Shetty K
[Ti] Título:In Vivo Microvascular Pattern of Solitary Juxtapapillary Capillary Hemangioma on OCT Angiography.
[So] Source:Ophthalmic Surg Lasers Imaging Retina;48(7):592-595, 2017 Jul 01.
[Is] ISSN:2325-8179
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Juxtapapillary capillary hemangioma (JCH) is a vascular hamartoma. Fluorescein fundus angiography aids in diagnosis. The vascular morphology of this tumor has not been documented with optical coherence tomography angiography (OCTA), a new, noninvasive diagnostic modality that provides high-resolution images of vascular pattern based on blood flow in the retina and choroid. Although mainly a clinical diagnosis, OCTA helps in studying the intrinsic vascularity of the tumor and helps in differentiating it from other vascular tumors. The authors report the case of a young male with unilateral solitary JCH and its microvascular pattern, as seen on OCTA. [Ophthalmic Surg Lasers Imaging Retina. 2017;48:592-595.].
[Mh] Termos MeSH primário: Corioide/patologia
Angiofluoresceinografia/métodos
Hemangioma Capilar/diagnóstico
Neoplasias da Retina/diagnóstico
Vasos Retinianos/patologia
Tomografia de Coerência Óptica/métodos
[Mh] Termos MeSH secundário: Adulto
Diagnóstico Diferencial
Fundo de Olho
Seres Humanos
Masculino
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170929
[Lr] Data última revisão:
170929
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170721
[St] Status:MEDLINE
[do] DOI:10.3928/23258160-20170630-12



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