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1.
Pediatr Surg Int ; 27(1): 103-6, 2011 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-20857299

RESUMEN

Tracheal agenesis is a very rare disorder which leads to severe respiratory disorders immediately after birth. Reports are very limited on long-term survival cases. We report here a long-term survival case with Floyd's type I tracheal agenesis. During the neonatal stage, the patient underwent abdominal esophageal banding to substitute esophagus for trachea and transection at the cervical esophagus with esophagostomy. Subsequently, airway management was difficult due to a fragile tracheoesophageal fistula, but the fistula was conservatively treated and stabilized with the patient's growth. This patient is a very rare case in whom oral feeding was achieved after esophageal reconstruction using a gastric tube. For this case, we describe mainly (1) the management method of the tracheoesophageal fistula and (2) esophageal reconstruction without thoracotomy.


Asunto(s)
Manejo de la Vía Aérea/métodos , Esófago/cirugía , Sobrevivientes , Fístula Traqueoesofágica/terapia , Constricción Patológica/complicaciones , Constricción Patológica/cirugía , Estudios de Seguimiento , Humanos , Recién Nacido , Masculino , Respiración con Presión Positiva/métodos , Tráquea/anomalías , Tráquea/cirugía , Fístula Traqueoesofágica/complicaciones , Resultado del Tratamiento
2.
Am J Case Rep ; 18: 1215-1219, 2017 Nov 16.
Artículo en Inglés | MEDLINE | ID: mdl-29142192

RESUMEN

BACKGROUND Around 20-30% of patients who undergo liver transplantation (LT) for alcoholic liver disease (ALD) will resume heavy drinking after LT. It is crucial to control post-transplant relapse of alcohol use, because alcoholic recidivism has been shown to have a negative impact on post-transplant compliance and long-term outcomes of LT recipients. However, there is currently no specific, effective psychiatric intervention for preventing additional alcohol consumption in clinical practice. CASE REPORT We present 3 patients who underwent LT for ALD at Nagoya University Hospital who were followed up for prolonged periods (7.2, 8.8, and 11.3 years, respectively), and review the psychiatric interventions employed to address critical situations. Additional alcohol consumption was noted in Case 1, but prompt collaborative care led to stable abstinence. In Case 2, marked anger and irritation were exacerbated as a result of work, but the anger was controlled by anger management. Case 3 abused a minor tranquilizer, but limit-setting resulted in adequate medical adherence. CONCLUSIONS Transplant teams need to provide comprehensive treatment for alcoholic recidivism to improve long-term health after LT for ALD.


Asunto(s)
Consumo de Bebidas Alcohólicas/prevención & control , Hepatopatías Alcohólicas/cirugía , Trasplante de Hígado , Receptores de Trasplantes/psicología , Adulto , Abstinencia de Alcohol , Alcoholismo/psicología , Continuidad de la Atención al Paciente , Femenino , Humanos , Masculino , Cooperación del Paciente
4.
PLoS One ; 9(2): e87722, 2014.
Artículo en Inglés | MEDLINE | ID: mdl-24498362

RESUMEN

The rate of graft survival has dramatically increased using calcineurin inhibitors, however chronic graft rejection and risk of infection are difficult to manage. Induction of allograft-specific regulatory T-cells (Tregs) is considered an ideal way to achieve long-term tolerance for allografts. However, efficient in vitro methods for developing allograft-specific Tregs which is applicable to MHC full-mismatched cardiac transplant models have not been established. We compared antigen-nonspecific polyclonal-induced Tregs (iTregs) as well as antigen-specific iTregs and thymus-derived Tregs (nTregs) that were expanded via direct and indirect pathways. We found that iTregs induced via the indirect pathway had the greatest ability to prolong graft survival and suppress angiitis. Antigen-specific iTregs generated ex vivo via both direct and indirect pathways using dendritic cells from F1 mice also induced long-term engraftment without using MHC peptides. In antigen-specific Treg transferred models, activation of dendritic cells and allograft-specific CTL generation were suppressed. The present study demonstrated the potential of ex vivo antigen-specific Treg expansion for clinical cell-based therapeutic approaches to induce lifelong immunological tolerance for allogeneic cardiac transplants.


Asunto(s)
Presentación de Antígeno/inmunología , Rechazo de Injerto/prevención & control , Enfermedad Injerto contra Huésped/prevención & control , Trasplante de Corazón , Linfocitos T Reguladores/inmunología , Linfocitos T Reguladores/trasplante , Traslado Adoptivo , Animales , Células Dendríticas/citología , Células Dendríticas/inmunología , Células Dendríticas/metabolismo , Rechazo de Injerto/inmunología , Supervivencia de Injerto , Enfermedad Injerto contra Huésped/inmunología , Ratones , Ratones Endogámicos BALB C , Ratones Endogámicos C57BL , Ratones Endogámicos CBA , Linfocitos T Reguladores/metabolismo , Trasplante Homólogo
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