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1.
World J Gastroenterol ; 21(19): 6032-43, 2015 May 21.
Artigo em Inglês | MEDLINE | ID: mdl-26019470

RESUMO

AIM: To evaluate the efficacy and safety of endoscopic submucosal dissection (ESD) for early gastric cancer (EGC) with undifferentiated-type histology. METHODS: A systematic literature review was conducted using the core databases. Complete resection, curative resection, en bloc resection, recurrence and adverse event rate were extracted and analyzed. A random effect model was applied. The methodological quality of the enrolled studies was assessed using the Newcastle-Ottawa Scale. Publication bias was evaluated using a funnel plot, the trim and fill method, Egger's test, and a rank correlation test. RESULTS: Fourteen retrospective studies between 2009 and 2014 were identified (972 EGC lesions with undifferentiated-type histology). The total en bloc and complete resection rates were estimated as 92.1% (95%CI: 87.4%-95.2%) and 77.5% (95%CI: 69.3%-84%), respectively. The total curative resection rate was 61.4% (95%CI: 44.5%-75.9%). The overall recurrence rate was 7.6% (95%CI: 3.4%-16%). Limited to histologically diagnosed expanded-criteria lesions, the en bloc and complete resection rates were 91.2% and 85.6%, respectively. The curative resection rate was 79.8%. CONCLUSION: In this analysis, ESD is a technically feasible treatment modality for EGC with undifferentiated-type histology. Long-term studies are needed to confirm these therapeutic outcomes.


Assuntos
Diferenciação Celular , Dissecação/métodos , Gastrectomia/métodos , Mucosa Gástrica/cirurgia , Gastroscopia/métodos , Neoplasias Gástricas/cirurgia , Distribuição de Qui-Quadrado , Dissecação/efeitos adversos , Gastrectomia/efeitos adversos , Mucosa Gástrica/patologia , Gastroscopia/efeitos adversos , Humanos , Estadiamento de Neoplasias , Razão de Chances , Medição de Risco , Fatores de Risco , Neoplasias Gástricas/patologia , Resultado do Tratamento
2.
Skeletal Radiol ; 39(6): 589-93, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20140429

RESUMO

Systemic hyalinosis is a rare, multisystem, progressive, autosomal recessive disorder of connective tissue characterized by diffuse hyaline deposition in the skin, bone or viscera. Owing to its rarity and initial manifestations that resemble arthrogryposis congenital multiplexa, correct diagnosis can be elusive and often delayed. We present the computed tomography (CT) and whole-body (WB) magnetic resonance (MR) findings in two unrelated children with systemic hyalinosis who came to medical attention because of multiple joint contractures and limitation of motion in early infancy.


Assuntos
Artrogripose/complicações , Artrogripose/diagnóstico , Glomerulosclerose Segmentar e Focal/complicações , Glomerulosclerose Segmentar e Focal/diagnóstico , Tomografia Computadorizada por Raios X , Diagnóstico Diferencial , Humanos , Lactente , Masculino
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