Congenital intrahepatic portosystemic shunts: a potential cause for early-onset neonatal cholestasis
Abstract: Cholestasis in the first days of life is uncommon in neonates. Neonatal cholestasis is usually associated with shock, sepsis, alloimmunity, metabolic disorders or biliary obstruction. A congenital intrahepatic portosystemic shunt results from failed involution of primordial liver vessels during the first days of life. Resulting shunts can lead to hepatic encephalopathy or liver tumors. A congenital intrahepatic portosystemic shunt should be considered when an alternative explanation cannot be found. In most cases, congenital intrahepatic portosystemic shunts will involute spontaneously by 1–2 years of age; however, surgical or radiologic closure may be needed.
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Erschienen in
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Congenital intrahepatic portosystemic shunts: a potential cause for early-onset neonatal cholestasis ; volume:7 ; number:1 ; year:2018 ; extent:4
Case reports in perinatal medicine ; 7, Heft 1 (2018) (gesamt 4)
- Urheber
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Narang, Radhika
Patel, Minal
Tipnis, Neelesh Ajit
Tipnis, Sajani Matai
- DOI
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10.1515/crpm-2017-0033
- URN
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urn:nbn:de:101:1-2411121527188.809126355268
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2300, 07:20 MESZ
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Beteiligte
- Narang, Radhika
- Patel, Minal
- Tipnis, Neelesh Ajit
- Tipnis, Sajani Matai
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