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1.
JSLS ; 19(1): e2015.00002, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-25848198

RESUMEN

BACKGROUND AND OBJECTIVES: Placement of surgical gastric access is a common operative procedure, with multiple techniques. We describe a cost-effective, safe, and easy-to-perform primary endoscopic gastrostomy button placement in the pediatric population, using a novel double-transcutaneous lasso U-stitch push technique. METHODS: This is a retrospective review of a single center's experience of 24 consecutively performed primary gastrostomy button placements in infants and children aged 3 weeks to 20 years, from October 2012 through October 2014. RESULTS: The procedure was generally well tolerated, with no intraoperative complications. No conversions to laparoscopic or open procedures were necessary. There were no early tube dislodgements and no postoperative complications within the first 4 weeks. CONCLUSION: The endoscopic primary gastrostomy button placement with a transcutaneous lasso U-stitch is a safe, fast, elegant, and cost-effective alternative to a standard percutaneous endoscopic gastrostomy placement.


Asunto(s)
Endoscopía Gastrointestinal/métodos , Gastrostomía/métodos , Técnicas de Sutura , Adolescente , Niño , Preescolar , Endoscopía Gastrointestinal/instrumentación , Femenino , Gastrostomía/instrumentación , Humanos , Lactante , Recién Nacido , Masculino , Evaluación de Resultado en la Atención de Salud , Estudios Retrospectivos , Adulto Joven
2.
Pediatr Surg Int ; 31(4): 417-9, 2015 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-25623596

RESUMEN

Serous microcystic adenoma of the pancreas is an uncommon tumor in adults, and reported in pediatric patients only a handful of times. The authors present a case of a 6 month patient with incidental finding of a large cystic mass on the tail of the pancreas during an operation for Hirschsprung's disease. Final pathology was consistent with serous microcystic adenoma. This is the second case report describing this lesion in an infant, and the first time it has been associated with Hirschsprung's disease.


Asunto(s)
Cistadenoma Seroso/etiología , Anomalías del Sistema Digestivo/complicaciones , Enfermedad de Hirschsprung/complicaciones , Vólvulo Intestinal/complicaciones , Neoplasias Pancreáticas/etiología , Cistadenoma Seroso/diagnóstico , Cistadenoma Seroso/cirugía , Anomalías del Sistema Digestivo/diagnóstico , Femenino , Enfermedad de Hirschsprung/diagnóstico , Humanos , Hallazgos Incidentales , Recién Nacido , Vólvulo Intestinal/diagnóstico , Pancreatectomía , Neoplasias Pancreáticas/diagnóstico , Neoplasias Pancreáticas/cirugía
3.
Ann Med Surg (Lond) ; 4(4): 467-9, 2015 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-26779336

RESUMEN

INTRODUCTION: Ciliated hepatic foregut cysts (CHFC) are rare congenital hepatic lesions derived from the embryonic foregut. Because of potential transformation to squamous cell carcinoma in adulthood, the mainstay of therapy is surgical resection. To our knowledge, we report the first case of CHFC in a child that was successfully excised laparoscopically. PRESENTATION OF CASE: We report a case of a 4-year-old boy that was diagnosed with an asymptomatic 5-cm liver cyst. After surveillance for 3 years, the cyst grew to 7 cm at which time it was successfully resected laparoscopically. The pathology was consistent with CHFC. DISCUSSION: There have been few previous reports of CHFCs in children, all of which described excision via a laparotomy. This is the first case report of laparoscopic resection of CHFC in a child. CONCLUSION: This case report suggests that laparoscopy may be safe and effective for resection of CHFCs with favorable anatomy such as peripheral location and noninvolvement of key vascular and biliary structures.

5.
JSLS ; 16(3): 401-5, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-23318065

RESUMEN

BACKGROUND AND OBJECTIVES: Multiple single-port or single-incision techniques have been successfully implemented for laparoscopic cholecystectomy in adults and children. These techniques require either a large multichannel port or a larger skin incision to accommodate multiple ports or instruments. Inspired by a first generation single-port instrument, we developed a safe and effective technique for a single-port laparoscopic cholecystectomy with virtually scarless results. METHODS: Over a 14-mo period, 20 patients (19 females, 1 male) underwent the hybrid single-port cholecystectomy. A straight 10-mm Storz telescope with inbuilt 6-mm working channel in combination with 2 portless 2.3-mm percutaneous graspers was used. The dissection is carried out with 43-cm bariatric length instruments. The cystic artery and duct are sealed with WECK Hem-o-lok clips or the Harmonic scalpel. RESULTS: Range (mean) age: 7.7 y to 19.5 y (15.5), BMI: 11.6kg/m(2) to 42.3kg/m(2) (27), operative duration 48 min to 120 min (79), postoperative length of stay: 5 h to 78 h (24). DIAGNOSIS: 13 patients cholecystolithiasis, 7 patients biliary dyskinesia. Conversion to conventional 4-port cholecystectomy was required in 2 patients. No intra- or postoperative complications occurred. CONCLUSION: The hybrid single-port technique is easy to master. It provides traditional anatomical exposure and allows application of conventional laparoscopic principles.


Asunto(s)
Colecistectomía Laparoscópica/instrumentación , Enfermedades de la Vesícula Biliar/cirugía , Laparoscopios , Adolescente , Niño , Diseño de Equipo , Femenino , Estudios de Seguimiento , Humanos , Masculino , Estudios Retrospectivos , Resultado del Tratamiento , Adulto Joven
6.
J Neurotrauma ; 28(8): 1525-43, 2011 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-20507235

RESUMEN

The past three decades have seen an explosion of research interest in spinal cord injury (SCI) and the development of hundreds of potential therapies that have demonstrated some promise in pre-clinical experimental animal models. A growing number of these treatments are seeking to be translated into human clinical trials. Conducting such a clinical trial, however, is extremely costly, not only for the time and money required to execute it, but also for the limited resources that will then no longer be available to evaluate other promising therapies. The decision about what therapies have sufficient pre-clinical evidence of efficacy to justify testing in humans is therefore of utmost importance. Here, we have developed a scoring system for objectively grading the body of pre-clinical literature on neuroprotective treatments for acute SCI. The components of the system include an evaluation of a number of factors that are thought to be important in considering the "robustness" of a therapy's efficacy, including the animal species and injury models that have been used to test it, the time window of efficacy, the types of functional improvements effected by it, and whether efficacy has been independently replicated. The selection of these factors was based on the results of a questionnaire that was performed within the SCI research community. A modified Delphi consensus-building exercise was then conducted with experts in pre-clinical SCI research to refine the criteria and decide upon how to score them. Finally, the grading system was applied to a series of potential neuroprotective treatments for acute SCI. This represents a systematic approach to developing an objective method of evaluating the extent to which the pre-clinical literature supports the translation of a particular experimental treatment into human trials.


Asunto(s)
Fármacos Neuroprotectores/uso terapéutico , Traumatismos de la Médula Espinal/terapia , Animales , Modelos Animales de Enfermedad , Humanos , Traumatismos de la Médula Espinal/tratamiento farmacológico
7.
J Pediatr Surg ; 42(11): 1841-4, 2007 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-18022433

RESUMEN

PURPOSE: Many different prosthetic materials have been used for repair of large posterolateral congenital diaphragmatic hernias (CDH), with high recurrence rates for hernias that cannot be primarily repaired. Since 1993, we have used a composite patch of Gore-Tex/Marlex to repair large CDHs and hypothesized that this repair leads to fewer recurrences. METHODS: This is a retrospective review of 137 consecutive patients with CDH cared for at a single institution from 1993 to 2004. Data collected include timing and method of repair and use of extracorporeal membrane oxygenation. Outcomes include hernia recurrence, complications, and death. RESULTS: One hundred thirty-seven patients with CDH were analyzed. Repair was not attempted in 12 because of disease severity. Primary repair was accomplished in 79 and 46 required patch repair. Of the 46 patients with patch repairs, 32 required extracorporeal membrane oxygenation, and 18 died before discharge. Of the 28 patch repair survivors, 1 (3.57%) developed a recurrence over a median follow-up of 47 months (range, 2-115 months). Overall survival was 77%. CONCLUSIONS: Gore-Tex/Marlex composite patch repair of large CDHs in this complex patient population results in a lower recurrence rate than has been reported for other types of prosthetic diaphragm repair.


Asunto(s)
Hernia Diafragmática/genética , Hernia Diafragmática/cirugía , Polipropilenos , Politetrafluoroetileno , Implantación de Prótesis/métodos , Estudios de Cohortes , Femenino , Estudios de Seguimiento , Hernia Diafragmática/mortalidad , Hernia Diafragmática/patología , Humanos , Recién Nacido , Laparotomía/métodos , Masculino , Recurrencia , Estudios Retrospectivos , Medición de Riesgo , Índice de Severidad de la Enfermedad , Mallas Quirúrgicas , Tasa de Supervivencia , Resistencia a la Tracción , Resultado del Tratamiento
8.
Mod Pathol ; 15(2): 172-80, 2002 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-11850547

RESUMEN

Proteus syndrome is a rare, sporadic disorder that causes postnatal overgrowth of multiple tissues in a mosaic pattern. Characteristic manifestations include: overgrowth and hypertrophy of limbs and digits, connective tissue nevus, epidermal nevus and hyperostoses. Various benign and malignant tumors and hamartomas may complicate the clinical course of patients with the syndrome. Commonly encountered tumors include hemangiomas, lymphangiomas and lipomas. Tumors of the genital tract occur less often. Bilateral ovarian cystadenomas are regarded as having diagnostic value in Proteus syndrome when occurring within the first two decades of life. We describe a 3-year-old girl with Proteus syndrome who developed bilateral paraovarian villoglandular endometrioid cystadenomatous tumors of borderline malignancy (low malignant potential) of the broad ligament. Desmoplastic tumor implants, presumably noninvasive, were present in biopsies from the pelvic floor, cul-de-sac and omentum. This is the first recognized example of a cystic borderline epithelial tumor of the female genital tract and the first paraovarian tumor reported in a patient with Proteus syndrome. Previously reported tumors and cystic lesions involving the female genital tract and the male genital tract in patients with Proteus syndrome are reviewed. We suspect that specific testicular and paratesticular tumors may prove to have the same diagnostic value in Proteus syndrome as do bilateral cystic ovarian and paraovarian tumors.


Asunto(s)
Carcinoma Endometrioide/patología , Quistes Ováricos/patología , Neoplasias Ováricas/patología , Síndrome de Proteo/patología , Preescolar , Femenino , Humanos
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