RESUMEN
BACKGROUND: Laparoscopic Kasai portoenterostomy (LKPE) is generally regarded to have a poorer outcome for surgical treatment of uncorrectable biliary atresia. We herein described our initial experience of some modifications to make LKPE easier in the treatment of type III biliary atresia (BA). METHODS: During the period July 2012-October 2016, a total of 25 infants with type III BA were treated with a modified LKPE technique. A percutaneous suture was introduced just below the xiphoid process to snare the round ligament and retract the liver; other percutaneous stay sutures were then introduced to the fundus and neck of the gallbladder to elevate the liver and expose the porta hepatis. In 15 cases, part of the hepatic lobus quadratus was removed laparoscopically to expose the porta hepatis. The two elastic rubber bands were put around the portal vein and hepatic artery, and the porta hepatis was exposed by stretching the two rubber bands laterally to facilitate laparoscopic portoenterostomy. RESULTS: Patients were divided into two groups according to their ages at operation: group I: age between 30 and 75 days (n = 18), and group II: age between 76 and 85 days (n = 8). There were no operative deaths, but two patients died of repeated cholangitis and liver failure. Blood loss during operation was minimal and no blood transfusions were required. Operating times varied from 210 to 270 min (mean 232.4 ± 19.0 min). Among the two groups, there were no differences in blood loss (P > 0.05), but there were differences in operating time (P < 0.05). All patients survived the surgery without any intraoperative complications, and the median follow-up time was 25.3 months. Total bilirubin dropped to normal in 18 patients with an additional 5 patients showing a significant overall drop after surgery. CONCLUSIONS: With the original concepts of Kasai portoenterostomy, perfect laparoscopic skills and some key modifications to expose the porta hepatis, our LKPE can be performed safely and successfully with improved outcome for infants with type III BA.
Asunto(s)
Atresia Biliar/cirugía , Laparoscopía/métodos , Portoenterostomía Hepática/métodos , Atresia Biliar/mortalidad , Pérdida de Sangre Quirúrgica/estadística & datos numéricos , Preescolar , Colangitis/epidemiología , Colangitis/etiología , Femenino , Estudios de Seguimiento , Humanos , Incidencia , Lactante , Laparoscopía/efectos adversos , Hígado/cirugía , Masculino , Tempo Operativo , Portoenterostomía Hepática/efectos adversos , Complicaciones Posoperatorias/epidemiología , Complicaciones Posoperatorias/etiología , Resultado del TratamientoRESUMEN
OBJECTIVES: Superior mesenteric artery syndrome (SMAS) is an uncommon cause of duodenal obstruction in pediatric patients. It is extremely rare in young infants. The classic treatment for SMAS has been an open or laparoscopic duodenojejunostomy when conservative medical therapy failed to resolve the obstruction. We herein reported 3 cases of SMAS in infants treated by laparoscopic Ladd's procedure. The advantages and feasibility of laparoscopic Ladd's procedure applied for SMAS in infants were discussed. METHODS: Three cases of infants with SMAS subjected to laparoscopic Ladd's procedure in our hospital were collected from January 2014 to December 2015. The patients' age, operative time, postoperative hospital observation, resumption of full diet, and postoperative complications were analyzed. RESULTS: The median age at operation was 8â¯months (range, 6-9â¯months). The mean body weight was 7.9â¯kg (range, 6.5-8.8â¯kg). The mean operative time was 66.7â¯min (range, 65-75â¯min). The mean postoperative hospital stay was 4.3â¯days (range, 4-5â¯days) and the follow-up was 20.7â¯months (range, 12-34â¯months) without any specific postoperative complications. CONCLUSION: Based on our reports, laparoscopic Ladd's procedure is a reliable and practicable minimally invasive surgery for in infants with SMAS.
Asunto(s)
Laparoscopía , Síndrome de la Arteria Mesentérica Superior , Femenino , Humanos , Lactante , Laparoscopía/efectos adversos , Laparoscopía/métodos , Tiempo de Internación/estadística & datos numéricos , Masculino , Nutrición Parenteral , Complicaciones Posoperatorias , Síndrome de la Arteria Mesentérica Superior/epidemiología , Síndrome de la Arteria Mesentérica Superior/cirugíaRESUMEN
Three female infants, aged 13, 7 and 18 mo respectively with acquired ileal atresia induced by adhesive small bowel obstruction are reported. Case 1 was diagnosed with urachal cyst and cyst excision was performed when she was 7-mo-old. Case 2 was diagnosed with mesenteric cyst and cyst excision was performed by laparoscopic-assisted procedure when she was 3-mo-old. Case 3 had no history of abdominal operation previously. At laparotomy ileal atresia induced by adhesive band was found.
Asunto(s)
Enfermedades del Íleon/etiología , Atresia Intestinal/complicaciones , Obstrucción Intestinal/complicaciones , Intestino Delgado/anomalías , Femenino , Humanos , Íleon , Lactante , Atresia Intestinal/etiología , Atresia Intestinal/patología , Obstrucción Intestinal/patología , Complicaciones PosoperatoriasRESUMEN
Prepyloric web is a rare diagnosis in pediatrics; only sporadic cases were described in the literature. Treatment is classically performed by open surgery; laparoscope-assisted diagnosis and treatment of prepyloric web in children have not been reported. Three cases with prepyloric web were diagnosed and treated by laparoscope-assisted procedure in our hospital from June 2009 to October 2010. There were no conversions to open surgery and no intraoperative various complications. After following up for 31-42 (mean 36.3) months postoperatively, the 3 infants remained asymptomatic and thriving. The early experiences suggest that the outcomes are excellent.
Asunto(s)
Laparoscopios , Píloro/anomalías , Píloro/cirugía , Anomalías Congénitas/diagnóstico , Obstrucción de la Salida Gástrica/diagnóstico , Obstrucción de la Salida Gástrica/etiología , Obstrucción de la Salida Gástrica/cirugía , Humanos , Lactante , MasculinoRESUMEN
Red blood cell transfusion is an effective method to treat acute hemorrhage and severe anemia. However, blood source from donors is very limited, and transfusion-transmitted diseases occurred frequently, thus threatening human health. Therefore, the safe, abundant and functional blood source is needed. Generation of blood cells from human pluripotent stem cells(hPSC) will offer alternative approach. Lots of studies have been focused on erythroid cell differentiation in vitro, including how to enhance efficiency and improve their function. In this review, the research advances on differentiation methods and the regulatory mechanism are summarized. In addition, the progress in PSC differentiation into erythrocytes and the problems to be solved are discussed briefly.