2017
DOI: 10.1016/j.ijscr.2017.10.044
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Gallbladder-associated symptomatic hepatic choristoma: Should you resect?

Abstract: HighlightsThe article represents symptomatic hepatic choristoma. To review the literature of this rare entity.To highlight the awareness of this unexpected finding and familiarity of its possible complications and malignant transformation.To emphasize that surgical treatment for the symptomatic and suspicious types of ectopic liver tissue mainly located outside the liver.

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Cited by 7 publications
(10 citation statements)
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“…ELT may be connected to the gallbladder wall by a handle containing blood vessels and bile ducts [5] . Because of the lack of well-developed blood vessels and excretory system, ELT has certain metabolic disorders, that can cause fatty change, haemosiderosis, cholestasis, or cirrhosis [2,12] . Moreover, same as the mother liver, ELT is exposed to carcinogens, [6] which include not only viral infection but also chemical carcinogens which cannot be completely excreted due to the poorly-developed blood vessel and excretory system of the ELT [13] , which adds to the increased risk of carcinogenesis [14] .…”
Section: Discussionmentioning
confidence: 99%
“…ELT may be connected to the gallbladder wall by a handle containing blood vessels and bile ducts [5] . Because of the lack of well-developed blood vessels and excretory system, ELT has certain metabolic disorders, that can cause fatty change, haemosiderosis, cholestasis, or cirrhosis [2,12] . Moreover, same as the mother liver, ELT is exposed to carcinogens, [6] which include not only viral infection but also chemical carcinogens which cannot be completely excreted due to the poorly-developed blood vessel and excretory system of the ELT [13] , which adds to the increased risk of carcinogenesis [14] .…”
Section: Discussionmentioning
confidence: 99%
“…EL has the same histopathology as the mother liver, including cirrhosis, hemosiderosis, hepatitis, and hepatocellular carcinoma (HCC) [ 3 ]. HCC was found in less than 5% of gallbladder cases associated with EL, and several cases had normal native liver tissue [ 7 , 14 ].…”
Section: Discussionmentioning
confidence: 99%
“…EL is a rare congenital anomaly lacking an anatomical connection to the liver proper [ 3 ]. EL is thought to be caused by an abnormal migration of hepatic tissue from the foregut diver-ticulum at cystic formations.…”
Section: Introductionmentioning
confidence: 99%
“…ELT is a rare congenital anomaly which lacks an anatomical connection to the liver proper. Its frequency is surprisingly low given the complexity of hepatogenesis which relies on hepatoblast migration . ELT is thought to arise from aberrant migration of hepatic tissue which develops together with cystic structures from a diverticulum of foregut.…”
mentioning
confidence: 99%
“…ELT is subject to the same pathology as native liver, such as hepatitis, hemosiderosis, cirrhosis and hepatocellular carcinoma (HCC) . However, ELT is less equipped to deal with parenchymal insults as it lacks a complete physiological hepatic architecture.…”
mentioning
confidence: 99%