Ruptured Hepatocellular Carcinoma in a Child with Budd-Chiari Syndrome.

dc.contributor.authorSuri, Anandini
dc.contributor.authorSharma, Varun K
dc.contributor.authorRanade, Prajakta R
dc.contributor.authorMarar, Shaji
dc.contributor.authorNagral, Aabha
dc.date.accessioned2016-12-02T10:41:14Z
dc.date.available2016-12-02T10:41:14Z
dc.date.issued2016-09
dc.description.abstractBackground: Hepatocellular carcinoma is an uncommon complication described in patients with Budd-Chiari syndrome. Case characteristics: A 12-year-old boy with Budd-Chiari syndrome, who was earlier treated with Transjugular intrahepatic porto-systemic shunt (TIPS), presented with acute onset hemoperitoneum and hypotension. Outcome: It was diagnosed to be a case of ruptured hepatocellular carcinoma. Message: Successful TIPS may not prevent the development of hepatocellular carcinoma, and children with Budd Chiari syndrome should be monitored for the same.en_US
dc.identifier.citationAnandini Suri, Varun K Sharma, Prajakta R Ranade, Shaji Marar and Aabha Nagral. Ruptured Hepatocellular Carcinoma in a Child with Budd-Chiari Syndrome. Indian Pediatrics. 2016 Sept; 53(9): 833-834.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/179233
dc.language.isoenen_US
dc.source.urihttps://www.indianpediatrics.net/sep2016/sep-833-834.htmen_US
dc.subjectComplicationen_US
dc.subjectHemoperitoneumen_US
dc.subjectLiver tumoren_US
dc.subjectTIPSen_US
dc.titleRuptured Hepatocellular Carcinoma in a Child with Budd-Chiari Syndrome.en_US
dc.typeArticleen_US
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