Results 131 to 140 of about 358,897 (181)
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Successful treatment of hepatic and mesh Aspergillosis in a neonate with giant omphalocele.
Journal de Mycologie Médicale, 2022Aspergillosis is a rare and life-threatening fungal infection in immunocompetent children, particularly in infants. We present a case of invasive Aspergillosis (IA) that developed hepatic and mesh infection due to Aspergillus flavus following the rupture
S. Arslan +9 more
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Management of Giant Omphalocele: A Case Series
European Journal of Pediatric Surgery, 2012Giant omphalocele (GO) is congenital abdominal wall defect measuring >6 cm and/or containing liver.[1] The omphalocele sac consists of amnion and peritoneum, and is prone to rupture either in utero, during delivery or after birth. The surgical management of neonates with GO is challenging.
Morgan, Robert; id_orcid 0000-0003-0612-0954 +2 more
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Amnion inversion in the treatment of giant omphalocele
Journal of Pediatric Surgery, 1991Operative repair of giant omphaloceles remains a technical challenge to close the wide abdominal wall defect. Currently, most surgeons remove the amnion to approximate the linea alba and/or skin edges or to suture prosthetic material to the abdominal wall and cover the defect with skin flaps.
A A, de Lorimier +2 more
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Breastfeeding Success in Infants With Giant Omphalocele
Advances in Neonatal Care, 2012Infants born with a giant omphalocele often require multiple surgeries requiring a lengthy hospital stay. These vulnerable infants may experience a long period of being NPO (nothing by mouth), followed by slowly advancing to enteral feeds. Human milk is the ideal method of nutrition for all infants and should be used to initiate enteral feeds in ...
Diane L, Spatz, Katherine J, Schmidt
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The use of Alloderm in the closure of a giant omphalocele
Journal of Pediatric Surgery, 2006Giant omphaloceles are associated with a considerable loss of abdominal domain. Early primary repair of the fascia is either not possible or poorly tolerated by the infant. Current surgical options result in a ventral hernia requiring future surgery or involve the chronic use of prosthetic patches with or without tissue expanders.
Samuel M, Alaish, Eric D, Strauch
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Giant Omphalocele Complicated by 9P Minus Syndrome
Journal of the National Medical Association, 2021Omphalocele is characterized as a ventral wall defect in which there exists a midline herniation of abdominal viscera into the base of the umbilical cord. Fetuses with a diagnosis of this entity are at a significantly increased risk of having an aneuploidy, additional anomalies, or associations with other syndromes such as Beckwith Wiederman. Secondary
Gabrielle, Alexander +5 more
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Paint and wait management of giant omphaloceles
Seminars in Pediatric Surgery, 2019Management of the very large defect or those in patients with severe comorbidities has evolved to the use of methods that result in escharification and eventual skin coverage over the viscera. This treatment strategy employs principles that were described in the early 20th century.
Justin P, Wagner, Robert A, Cusick
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Repair of a giant omphalocele by a modified technique
Pediatric Surgery International, 2000Large omphaloceles that contain centrally herniated liver pose challenges to surgical closure, the most significant being the space limitation of the abdominal cavity. In addition, the "pedicled" nature of the liver on the inferior vena cava creates a predisposition to acute hepatic vascular outflow obstruction as the liver is reduced into the ...
M M, Harjai +4 more
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Sequential sac ligation for giant omphalocele
Journal of Pediatric Surgery, 1994The authors describe a technique for the management of giant omphalocele in which the sac is not resected, but used to sequentially reduce the contents into the abdominal cavity. Three patients were treated in this fashion. Delayed primary fascial closure was achieved in two.
A R, Hong +4 more
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Pulmonary hypertension in giant omphalocele infants
Journal of Pediatric Surgery, 2014Pulmonary hypoplasia has been described in cases of giant omphalocele (GO), although pulmonary hypertension (PH) has not been extensively studied in this disorder. In the present study, we describe rates and severity of PH in GO survivors who underwent standardized prenatal and postnatal care at our institution.A retrospective chart review was ...
Emily A, Partridge +7 more
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