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1.
Pediatr Crit Care Med ; 18(3): 272-280, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28079652

RESUMO

OBJECTIVE: Extracorporeal membrane oxygenation has been used in patients with severe circulatory or respiratory failure since the 1970s, but the knowledge on long-term survival in this group is scarce. The aim of the present study was to investigate the 10-year survival rates and causes of late death in children treated with extracorporeal membrane oxygenation. DESIGN: Single-center, retrospective cohort study. SETTING: Tertiary referral center for extracorporeal life support. PATIENTS: Neonatal and pediatric patients treated with extracorporeal membrane oxygenation from 1987 to December 2013. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: Survival status was obtained from the national Causes of Death registry. Patient background data along with data on survival and causes of death were collected. Survival rates were calculated using the Kaplan-Meier method. Of 400 subjects, 76% survived to discharge. The median follow-up time in survivors was 7.2 years. There was a high mortality rate within the first months after discharge. In the group of patients who survived the first 90 days after treatment, the 10-year survival rates were 93% in neonates and 89% in pediatric patients and were particularly beneficial in patients whose indication for extracorporeal membrane oxygenation was meconium aspiration syndrome, trauma, or infectious diseases. Late deaths were seen in some diagnostic groups, but the Kaplan-Meier curves plateaued over time. CONCLUSIONS: Children who survive the first months after treatment with extracorporeal membrane oxygenation have a high long-term survival rate. The prognosis is especially favorable in patients with reversible conditions.


Assuntos
Cuidados Críticos , Oxigenação por Membrana Extracorpórea/mortalidade , Insuficiência Respiratória/terapia , Choque/terapia , Adolescente , Causas de Morte , Criança , Pré-Escolar , Feminino , Seguimentos , Humanos , Lactente , Unidades de Terapia Intensiva Pediátrica , Estimativa de Kaplan-Meier , Masculino , Insuficiência Respiratória/mortalidade , Estudos Retrospectivos , Choque/mortalidade , Taxa de Sobrevida
2.
Int J Surg Pathol ; 23(7): 579-84, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26215223

RESUMO

Desmoid tumors, also known as desmoid-type fibromatoses or aggressive fibromatoses, are clonal fibroblastic proliferations that arise in the deep soft tissues. They are characterized by infiltrative growth, a tendency toward local recurrence and the inability to metastasize. We present a case of a 63-year-old woman who complained of abdominal pain, and a contrast-enhanced computed tomography scan revealed a well-circumscribed tumor in the pancreatic tail, measuring 5.1 cm. A left-sided, spleen-preserving pancreatic resection was performed, and pathological analysis showed a mesenchymal tumor. The diagnosis of a pancreatic desmoid tumor was made based on the characteristic morphology and the immune phenotype of the tumor. The English-language literature on pancreatic desmoid tumors was reviewed. In total, 16 previous cases were identified.


Assuntos
Fibromatose Agressiva/patologia , Pâncreas/patologia , Neoplasias Pancreáticas/patologia , Biomarcadores Tumorais/metabolismo , Feminino , Fibromatose Agressiva/metabolismo , Humanos , Pessoa de Meia-Idade , Pâncreas/metabolismo , Neoplasias Pancreáticas/metabolismo
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