Supradiaphragmatic Right Liver Lobe and Gallbladder

Organ, Claude H.; Hayes, Dennis F.

doi:10.1001/archsurg.1980.01380080079017

Cited by 7 publications

(4 citation statements)

References 3 publications

Supporting

Mentioning

Contrasting

Unclassified

Order By: Relevance

“…[15][16][17] A unique case of a supradiaphragmatic right liver lobe and gallbladder has been reported. 18 Partial eventration of the right hemidiaphragm is a congenital lesion caused by aplasia or hypoplasia of part of the musculature of the diaphragm with resultant bulging of the affected portion from intra-abdominal pressure. 19 The underlying portion of the liver prolapses into the diaphragmatic pouch where it may become strangulated.…”

Section: Anomalies Of Positionmentioning

confidence: 99%

“…202 It may represent yet another disease mechanism for BA, distinct from those represented by early-and late-pattern BA, although cystic BA has been identified in patients with early-pattern (fetal/embryonal) BA. Some infants with BA have specific chromosomal abnormalities such as trisomy [17][18]203 Turner syndrome, 204 or cat-eye syndrome. 205 A lethal autosomal recessive syndrome with intra-uterine growth retardation, intra-and extrahepatic BA, and oesophageal and duodenal atresia was reported in one family.…”

Section: Spontaneous Bile Duct Perforationmentioning

confidence: 99%

See 1 more Smart Citation

Developmental abnormalities and liver disease in childhood

Portmann¹,

Roberts²

2012

MacSween's Pathology of the Liver

View full text Add to dashboard Cite

Section: Anomalies Of Positionmentioning

confidence: 99%

Section: Spontaneous Bile Duct Perforationmentioning

confidence: 99%

Developmental abnormalities and liver disease in childhood

Portmann¹,

Roberts²

2012

MacSween's Pathology of the Liver

View full text Add to dashboard Cite

“…10. № 1 полости, полости перикарда, пупочной грыже, сальнике и ретроперитонеальном пространстве [28][29][30][31][32]. Достаточно редкий случай описан G. Johnstone в 1965 г.…”

Section: Discussionunclassified

Results of operative treatment of omphalocele with an additional lobe of the liver, and pyloric stenosis

Щукина

Александровна²,

Mokrushina

et al. 2020

Russian Journal of Pediatric Surgery, Anesthesia and Intensive

View full text Add to dashboard Cite

Purpose. Presentation of clinical cases of rare combination of omphalocele with pylorostenosis in the postoperative period and additional liver lobe. Materials and methods. In National Medical Research Center for Childrens Health of health surgical ward of newborns and infants for the 2019 us operated 2 children who performed surgery involving intra-operative decision making about further surgical tactics. Results. the results of surgical treatment of newborns with omphalocele combined with hypertrophic pylorostenosis and extra liver lobe are presented. Conclusions. In patients with malformations of the anterior abdominal wall in the postoperative period, when regurgitation syndrome appears, it is necessary to make a differential diagnosis between the functional and organic causes of obstruction. When confirming the organic nature of the obstruction, surgical intervention is indicated. It is necessary to be able to timely and objectively assess the risks and expediency of the approach when choosing surgical tactics in each individual case.

show abstract

“…[2320][2321][2322] A unique case of a supradiaphragmatic right liver lobe and gallbladder has been reported. 2323 Partial eventration of the right hemidiaphragm is a congenital lesion caused by aplasia or hypoplasia of part of the musculature of the diaphragm, with resultant bulging of the affected portion from intra-abdominal pressure. 2324 The underlying portion of the liver prolapses into the diaphragmatic pouch, where it may become strangulated.…”

Section: Anomalies Of Positionmentioning

confidence: 99%

Developmental and Inherited Liver Disease

Quaglia¹,

Roberts²,

Torbenson³

2018

Macsween's Pathology of the Liver

View full text Add to dashboard Cite

Diagnostic approach to histology 113 Neonatal and early infantile liver disease 113 Postneonatal, childhood and adulthood presentation 118 Neonatal hepatitis 119 Histopathological features 120 Biliary atresia 121 Classification and aetiopathogenesis 121 Pathological features at surgical intervention 124 Pathology of intrahepatic changes 126 Paucity of intrahepatic bile ducts 129 Alagille syndrome (arteriohepatic dysplasia) 129 Nonsyndromic duct paucity disorders 131 Bile duct anomalies, congenital dilations and ductal plate malformation disorders 131 Choledochal cyst 132 Hereditary fibropolycystic disease (ductal plate malformation) 133 Cystic fibrosis 141 Hereditary disorders of bile acid synthesis and bilirubin metabolism 143 Primary disorders of bile acid synthesis 143 Disorders of bile canalicular transporters 146 Other diseases causing intrahepatic cholestasis 150 Hereditary defects of bilirubin metabolism 151 Disorders of porphyrin metabolism 153 Porphyria cutanea tarda 154 Erythropoietic protoporphyria 155 Disorders of carbohydrate metabolism and related conditions 156 Glycogen storage diseases (glycogenoses) 156 Myoclonus epilepsy, Lafora type (Lafora disease) 161 Galactosaemia Hereditary fructose intolerance Disorders of glycoprotein and glycolipid metabolism Mucopolysaccharidoses Aspartylglucosaminuria α-Mannosidosis Fucosidosis Mucolipidoses Congenital disorders of glycosylation (carbohydrate-deficient glycoprotein syndrome) Endoplasmic reticulum storage diseases α1-Antitrypsin deficiency α1-Antichymotrypsin deficiency Afibrinogenaemia and hypofibrinogenaemia Antithrombin III deficiency Disorders of amino acid metabolism Hereditary tyrosinaemia type 1 Congenital hyperammonaemia syndromes and urea cycle disorders Cystinosis Homocystinuria (cystathionine β-synthase deficiency) Disorders of lipoprotein and lipid metabolism Abetalipoproteinaemia Familial hypobetalipoproteinaemia Familial high-density lipoprotein deficiency (Tangier disease) Familial hypercholesterolaemia Wolman disease and cholesteryl ester storage disease Gangliosidoses α-Galactosidase A deficiency (Fabry disease) Sulphatide lipidosis (metachromatic leucodystrophy) Chapter 3 Developmental and Inherited Liver Disease

show abstract

Supradiaphragmatic Right Liver Lobe and Gallbladder

Cited by 7 publications

References 3 publications

Developmental abnormalities and liver disease in childhood

Developmental abnormalities and liver disease in childhood

Results of operative treatment of omphalocele with an additional lobe of the liver, and pyloric stenosis

Developmental and Inherited Liver Disease

Contact Info

Product

Resources

About