Search results for "abdominal wall defect"

showing 6 items of 6 documents

Predictive Factors of Abdominal Compartment Syndrome in Neonatal Age

2014

In the pediatric population, abdominal compartment syndrome (ACS) is a known complication of abdominal wall defect repair. However, there are only few reports on ACS in newborns and only a proposal of critical intra-abdominal pressure value (IAP) in term newborns, absent in preterm newborns. Although the prevalent clinical sign is tense abdominal distension, it may be difficult to distinguish ACS from pathologies that will not require decompression. The purpose of this study was to identify predictors for ACS and therefore morbidity or mortality indicators. We reviewed newborns presenting with tense abdominal distension and end organ failure. Anamnestic, clinical, laboratory, and instrument…

MalePediatricsmedicine.medical_specialtyNeonatal intensive care unitAbdominal compartment syndromePopulationGestational AgeAbdominal wallSettore MED/38 - Pediatria Generale E SpecialisticaIntubation IntratrachealHumansMedicineLactic AcideducationAbdominal Compartment Syndrome Predictive Factors in Neonatal AgeRetrospective Studieseducation.field_of_studybusiness.industryIncidenceAbdominal wall defectAbdominal WallInfant NewbornObstetrics and GynecologyGestational ageAbdominal distensionmedicine.diseaseRespiration ArtificialSurgerymedicine.anatomical_structureCase-Control StudiesPediatrics Perinatology and Child HealthApgar ScoreFemaleIntra-Abdominal HypertensionIntra-Abdominal Hypertensionmedicine.symptombusinessAmerican Journal of Perinatology
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An unusual association of left‐sided gastroschisis and persistent right umbilical vein

2018

Key Clinical Message Gastroschisis is a full‐thickness congenital abdominal wall defect usually occurring to the right of the umbilicus. About twenty cases of left‐sided gastroschisis have been reported, without reference to the laterality of the umbilical vein. This first case highlights the importance of considering and reporting this association by the perinatal team.

medicine.medical_specialtyprenatal diagnosisGastroschisisbusiness.industryUmbilicus (mollusc)Abdominal wall defectPrenatal diagnosisGeneral Medicinegastrointestinal malformation030204 cardiovascular system & hematologymedicine.diseaseLeft sidedUmbilical veinRight umbilical veinSurgery03 medical and health sciencesabdominal wall defect0302 clinical medicineClinical Images030220 oncology & carcinogenesisClinical ImageLateralitymedicinebusinessClinical Case Reports
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Meconial peritonitis in a rare association of partial ileal apple-peel atresia with small abdominal wall defect.

2014

Intestinal atresia type III B (apple peel) and gastroschisis are both congenital malformations who require early surgical correction in neonatal age. Their association is very rare. We present the case of a full term infant with partial apple peel ileal atresia and a small defect of the anterior abdominal wall, complicated by in utero intestinal perforation and subsequent meconial peritonitis. We observed a partial atresia of small intestine, with involvement of terminal ileus savings of jejunum and a large part of the proximal ileum, small anterior abdominal wall defect with herniation of few bowel loops, intestinal malrotation. Paralytic ileus and infections are the main causes of morbidi…

MaleMeconiummedicine.medical_specialtyIleuslcsh:SurgeryIntestinal AtresiaBacteremiaPeritonitisAbdominal wallFatal Outcomeapple-peelnewbornIleummedicinemeconial peritonitisHumansmeconium peritonitis neonatebusiness.industryGastroschisisAbdominal wall defectSettore MED/20 - Chirurgia Pediatrica E InfantileIntestinal atresiaAbdominal Wallgastroschisislcsh:RJ1-570Infant NewbornIleal Atresialcsh:Pediatricslcsh:RD1-811medicine.diseaseSurgeryHernia AbdominalAbdominal wall defectmedicine.anatomical_structureIntestinal malrotationIntestinal PerforationAtresiaPediatrics Perinatology and Child HealthUterine PerforationSurgeryFemalebusinessLa Pediatria medica e chirurgica : Medical and surgical pediatrics
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Recognizable neonatal clinical features of aplasia cutis congenita

2020

Abstract Background Aplasia cutis congenita (ACC), classified in nine groups, is likely to be underreported, since milder isolated lesions in wellbeing newborns could often be undetected, and solitary lesions in the context of polymalformative syndromes could not always be reported. Regardless of form and cause, therapeutic options have in common the aim to restore the deficient mechanical and immunological cutaneous protection and to limit the risk of fluid leakage or rupture of the exposed organs. We aimed to review our institutional prevalence, comorbidities, treatment and outcome of newborns with ACC. Methods We conducted a retrospective study including all newborns affected by ACC and …

Male0301 basic medicinePediatricsmedicine.medical_specialtyMeningomyeloceleAbdominal compartment syndromeContext (language use)030105 genetics & heredityAplasia cutis congenita03 medical and health sciencesEctodermal DysplasiaPrevalenceHumansMedicineBody Weights and MeasuresRetrospective StudiesPregnancybusiness.industryResearchAbdominal wall defectInfant Newbornlcsh:RJ1-570Gestational agelcsh:PediatricsRetrospective cohort studyPrognosismedicine.diseaseSurvival RateAbdominal wall defectRetrospective study030104 developmental biologyItalyScalp defectFemaleApgar scoreJunctional epidermolysis bullosamedicine.symptombusiness
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Perinatal management of gastroschisis

2014

Gastroschisis is an abdominal wall defect, typically located to the right of the umbilical cord, requiring an early surgical treatment shortly after birth. Affected patients can be identified during intrauterine life with US and should be delivered in referral hospitals where a multisciplinary approach can be provided, involving neonatologists, clinical geneticists, surgeons and other specialists. These patients require a complex management in Neonatal Intensive Care Unit (NICU) and a long term follow-up after discharge. Exceed the acute neonatal condition, gastroschisis has a good prognosis, if there are no overlapping complications, and it should be differentiated from omphalocele, burden…

abdominal wall defectmalformationprenatal diagnosisSettore MED/38 - Pediatria Generale E Specialisticanewbornsurgical treatmentlcsh:RSettore MED/20 - Chirurgia Pediatrica E Infantilelcsh:RJ1-570Abdominal wall defect prenatal diagnosis newborn malformation intensive care surgical treatmentlcsh:Medicinelcsh:Pediatricsintensive care
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Peritonite meconiale in una rara associazione di atresia ileale apple-peel con difetto di parete addominale

2014

L’atresia intestinale tipo III B (apple peel) e la gastroschisi sono entrambe malformazioni congenite che necessitano di correzione chirurgica precoce in epoca neonatale. La loro associazione è un evento molto raro. Presentiamo il caso di un neonato a termine con l’associazione di atresia ileale apple-peel parziale e piccolo difetto della parete addominale anteriore, complicate con perforazione intestinale in utero e conseguente peritonite meconiale. Abbiamo riscontrato un’atresia parziale delle anse intestinali, coninteressamento dell’ileo terminale e risparmio del digiuno e di buona parte dell’ileo prossimale, difetto della parete addominale di piccole dimensioni e con poche anse erniate,…

Settore MED/38 - Pediatria Generale E Specialisticaabdominal wall defect gastroschisis intestinal atresia apple-peel meconial peritonitis newbornSettore MED/20 - Chirurgia Pediatrica E Infantile
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