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Duplication of the Gallbladder: A Rare Congenital Anomaly
ABSTRACT Biliary tract shows a large number of anatomic variations and duplication of the gallbladder (GB) is a rare congenital anomaly. Although it is very often detected incidentally, it may present with complications due to gall stone disease. Careful identification of this anomaly on imaging is...
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Published in: | Annals of the National Academy of Medical Sciences (India) 2018-07, Vol.54 (3), p.175-178, Article 175 |
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creator | KS, Madhusudhan Srivastava, Saumya Srivastava, Deep N |
description | ABSTRACT
Biliary tract shows a large number of anatomic variations and duplication of the gallbladder (GB) is a rare congenital anomaly. Although it is very often detected incidentally, it may present with complications due to gall stone disease. Careful identification of this anomaly on imaging is important to prevent any serious surgical complications. We here report a case of duplicated GB in a 26-year-old male, who presented with right hypochondriac pain and detected to have two GB on magnetic resonance imaging (MRI). |
doi_str_mv | 10.1055/s-0040-1712844 |
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Biliary tract shows a large number of anatomic variations and duplication of the gallbladder (GB) is a rare congenital anomaly. Although it is very often detected incidentally, it may present with complications due to gall stone disease. Careful identification of this anomaly on imaging is important to prevent any serious surgical complications. We here report a case of duplicated GB in a 26-year-old male, who presented with right hypochondriac pain and detected to have two GB on magnetic resonance imaging (MRI).</description><identifier>ISSN: 0379-038X</identifier><identifier>EISSN: 2454-5635</identifier><identifier>DOI: 10.1055/s-0040-1712844</identifier><language>eng</language><publisher>A-12, Second Floor, Sector -2, NOIDA -201301, India: Thieme Medical and Scientific Publishers Private Ltd</publisher><subject>biliary anomalies ; cholelithiasis ; gallbladder duplication ; Original Article</subject><ispartof>Annals of the National Academy of Medical Sciences (India), 2018-07, Vol.54 (3), p.175-178, Article 175</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1834-f2447df6bbc0e234817c3387332a9db85516240fbe017b46ff3873e1d6ef29043</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0040-1712844.pdf$$EPDF$$P50$$Gthieme$$Hfree_for_read</linktopdf><link.rule.ids>314,780,784,20891,27924,27925,54587</link.rule.ids></links><search><creatorcontrib>KS, Madhusudhan</creatorcontrib><creatorcontrib>Srivastava, Saumya</creatorcontrib><creatorcontrib>Srivastava, Deep N</creatorcontrib><title>Duplication of the Gallbladder: A Rare Congenital Anomaly</title><title>Annals of the National Academy of Medical Sciences (India)</title><addtitle>Ann Natl Acad Med Sci</addtitle><description>ABSTRACT
Biliary tract shows a large number of anatomic variations and duplication of the gallbladder (GB) is a rare congenital anomaly. Although it is very often detected incidentally, it may present with complications due to gall stone disease. Careful identification of this anomaly on imaging is important to prevent any serious surgical complications. We here report a case of duplicated GB in a 26-year-old male, who presented with right hypochondriac pain and detected to have two GB on magnetic resonance imaging (MRI).</description><subject>biliary anomalies</subject><subject>cholelithiasis</subject><subject>gallbladder duplication</subject><subject>Original Article</subject><issn>0379-038X</issn><issn>2454-5635</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>0U6</sourceid><sourceid>DOA</sourceid><recordid>eNp1kMtqAkEQRZuQQMS4zXp-oE1VP2eyE_MShEBIILumpx86Mk5Lz7jw76NRssuqoOreA3UIuUeYIkj50FMAARQ1slKIKzJiQgoqFZfXZARcVxR4-X1LJn2_AQCUChBhRKqn_a5tnB2a1BUpFsM6FK-2bevWeh_yYzErPmwOxTx1q9A1g22LWZe2tj3ckZto2z5MLnNMvl6eP-dvdPn-upjPltRhyQWNTAjto6prB4FxUaJ2nJeac2YrX5dSomICYh0AdS1UjKdjQK9CZBUIPiaLM9cnuzG73GxtPphkG_O7SHllbB4a1wbjXeWkxiNZM6ExVswqpxA8LyN4wCNrema5nPo-h_jHQzAnj6Y3J4_m4vFYoOfCsG7CNphN2ufu-O1_-R8zjXBF</recordid><startdate>201807</startdate><enddate>201807</enddate><creator>KS, Madhusudhan</creator><creator>Srivastava, Saumya</creator><creator>Srivastava, Deep N</creator><general>Thieme Medical and Scientific Publishers Private Ltd</general><general>Thieme Medical and Scientific Publishers Pvt. Ltd</general><scope>0U6</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>DOA</scope></search><sort><creationdate>201807</creationdate><title>Duplication of the Gallbladder: A Rare Congenital Anomaly</title><author>KS, Madhusudhan ; Srivastava, Saumya ; Srivastava, Deep N</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1834-f2447df6bbc0e234817c3387332a9db85516240fbe017b46ff3873e1d6ef29043</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>biliary anomalies</topic><topic>cholelithiasis</topic><topic>gallbladder duplication</topic><topic>Original Article</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KS, Madhusudhan</creatorcontrib><creatorcontrib>Srivastava, Saumya</creatorcontrib><creatorcontrib>Srivastava, Deep N</creatorcontrib><collection>Thieme Connect Journals Open Access</collection><collection>CrossRef</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Annals of the National Academy of Medical Sciences (India)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KS, Madhusudhan</au><au>Srivastava, Saumya</au><au>Srivastava, Deep N</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Duplication of the Gallbladder: A Rare Congenital Anomaly</atitle><jtitle>Annals of the National Academy of Medical Sciences (India)</jtitle><addtitle>Ann Natl Acad Med Sci</addtitle><date>2018-07</date><risdate>2018</risdate><volume>54</volume><issue>3</issue><spage>175</spage><epage>178</epage><pages>175-178</pages><artnum>175</artnum><issn>0379-038X</issn><eissn>2454-5635</eissn><abstract>ABSTRACT
Biliary tract shows a large number of anatomic variations and duplication of the gallbladder (GB) is a rare congenital anomaly. Although it is very often detected incidentally, it may present with complications due to gall stone disease. Careful identification of this anomaly on imaging is important to prevent any serious surgical complications. We here report a case of duplicated GB in a 26-year-old male, who presented with right hypochondriac pain and detected to have two GB on magnetic resonance imaging (MRI).</abstract><cop>A-12, Second Floor, Sector -2, NOIDA -201301, India</cop><pub>Thieme Medical and Scientific Publishers Private Ltd</pub><doi>10.1055/s-0040-1712844</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | biliary anomalies cholelithiasis gallbladder duplication Original Article |
title | Duplication of the Gallbladder: A Rare Congenital Anomaly |
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