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Xanthogranulomatous cholecystitis: Diagnosis and management
•Xanthogranulomatous cholecystitis is a rare benign disease that can take on a pseudo-tumoral aspect.•It generally occurs in adults over 50.•Its etiopathogenesis is poorly defined.•Its association with gallbladder carcinoma remains controversial.•The best diagnostic imaging tool for xanthogranulomat...
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Published in: | Journal of visceral surgery 2021-08, Vol.158 (4), p.326-336 |
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description | •Xanthogranulomatous cholecystitis is a rare benign disease that can take on a pseudo-tumoral aspect.•It generally occurs in adults over 50.•Its etiopathogenesis is poorly defined.•Its association with gallbladder carcinoma remains controversial.•The best diagnostic imaging tool for xanthogranulomatous cholecystitis is magnetic resonance imaging.•Treatment is laparoscopic cholecystectomy, total or partial, with a high risk of conversion and complications.•In case of suspicion of xanthogranulomatous cholecystitis, a hepato-biliary specialty center should be involved.
Xanthogranulomatous cholecystitis (XGC) is a rare form of cholecystitis, characterized by the presence of xanthogranuloma, prominent yellow structures within the gallbladder wall that is very often lithiasic. When XGC presents in its pseudo-tumoral form with occasional adjacent organ involvement, it can mimic gallbladder carcinoma (GBC). The etiopathogenesis of XGC is inflammatory destruction of Rokitansky-Aschoff sinuses containing biliary and cholesterol pigments within the gallbladder wall; this leads to a florid granulomatous histiocytic inflammatory reaction. The prevalence ranges from 1.3% to 8.8% of all cholecystectomies and varies from country to country; XGC occurs predominantly in patients over 50 years of age, and is equally distributed between males and females. Its association with GBC remains a topic of debate in the literature (between 0 and 20%). Symptoms are non-specific and generally similar to those of acute or chronic cholecystitis. XGC, when associated with altered health status, leads to the suspicion of GBC. XGC can also come to light due to an acute complication of cholecystolithiasis, in particular, gallstone migration. Imaging by sonography and CT scan is suggestive, but magnetic resonance imaging is more specific. In difficult cases, biopsy may be necessary to eliminate the diagnosis of tumor. In case of pre- or intra-operative diagnostic doubt, the opinion of a hepatobiliary specialty center can be of help. When diagnosis of GBC has been eliminated, laparoscopic cholecystectomy is recommended, although with a high risk of conversion to laparotomy and complications. |
doi_str_mv | 10.1016/j.jviscsurg.2021.02.004 |
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Xanthogranulomatous cholecystitis (XGC) is a rare form of cholecystitis, characterized by the presence of xanthogranuloma, prominent yellow structures within the gallbladder wall that is very often lithiasic. When XGC presents in its pseudo-tumoral form with occasional adjacent organ involvement, it can mimic gallbladder carcinoma (GBC). The etiopathogenesis of XGC is inflammatory destruction of Rokitansky-Aschoff sinuses containing biliary and cholesterol pigments within the gallbladder wall; this leads to a florid granulomatous histiocytic inflammatory reaction. The prevalence ranges from 1.3% to 8.8% of all cholecystectomies and varies from country to country; XGC occurs predominantly in patients over 50 years of age, and is equally distributed between males and females. Its association with GBC remains a topic of debate in the literature (between 0 and 20%). Symptoms are non-specific and generally similar to those of acute or chronic cholecystitis. XGC, when associated with altered health status, leads to the suspicion of GBC. XGC can also come to light due to an acute complication of cholecystolithiasis, in particular, gallstone migration. Imaging by sonography and CT scan is suggestive, but magnetic resonance imaging is more specific. In difficult cases, biopsy may be necessary to eliminate the diagnosis of tumor. In case of pre- or intra-operative diagnostic doubt, the opinion of a hepatobiliary specialty center can be of help. When diagnosis of GBC has been eliminated, laparoscopic cholecystectomy is recommended, although with a high risk of conversion to laparotomy and complications.</description><identifier>ISSN: 1878-7886</identifier><identifier>EISSN: 1878-7886</identifier><identifier>DOI: 10.1016/j.jviscsurg.2021.02.004</identifier><identifier>PMID: 33741306</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Adenocarcinoma ; Cholecystectomy ; Gallbladder ; Rokitansky-Aschoff sinus ; Xanthogranulomatous cholecystitis</subject><ispartof>Journal of visceral surgery, 2021-08, Vol.158 (4), p.326-336</ispartof><rights>2021 Elsevier Masson SAS</rights><rights>Copyright © 2021 Elsevier Masson SAS. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-6fc52c8f773d4cf73652c5ae02271a4a77a2203ecce4ed6d96a94e80f9aa7d783</citedby><cites>FETCH-LOGICAL-c371t-6fc52c8f773d4cf73652c5ae02271a4a77a2203ecce4ed6d96a94e80f9aa7d783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33741306$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Giudicelli, X.</creatorcontrib><creatorcontrib>Rode, A.</creatorcontrib><creatorcontrib>Bancel, B.</creatorcontrib><creatorcontrib>Nguyen, A.-T.</creatorcontrib><creatorcontrib>Mabrut, J.-Y.</creatorcontrib><title>Xanthogranulomatous cholecystitis: Diagnosis and management</title><title>Journal of visceral surgery</title><addtitle>J Visc Surg</addtitle><description>•Xanthogranulomatous cholecystitis is a rare benign disease that can take on a pseudo-tumoral aspect.•It generally occurs in adults over 50.•Its etiopathogenesis is poorly defined.•Its association with gallbladder carcinoma remains controversial.•The best diagnostic imaging tool for xanthogranulomatous cholecystitis is magnetic resonance imaging.•Treatment is laparoscopic cholecystectomy, total or partial, with a high risk of conversion and complications.•In case of suspicion of xanthogranulomatous cholecystitis, a hepato-biliary specialty center should be involved.
Xanthogranulomatous cholecystitis (XGC) is a rare form of cholecystitis, characterized by the presence of xanthogranuloma, prominent yellow structures within the gallbladder wall that is very often lithiasic. When XGC presents in its pseudo-tumoral form with occasional adjacent organ involvement, it can mimic gallbladder carcinoma (GBC). The etiopathogenesis of XGC is inflammatory destruction of Rokitansky-Aschoff sinuses containing biliary and cholesterol pigments within the gallbladder wall; this leads to a florid granulomatous histiocytic inflammatory reaction. The prevalence ranges from 1.3% to 8.8% of all cholecystectomies and varies from country to country; XGC occurs predominantly in patients over 50 years of age, and is equally distributed between males and females. Its association with GBC remains a topic of debate in the literature (between 0 and 20%). Symptoms are non-specific and generally similar to those of acute or chronic cholecystitis. XGC, when associated with altered health status, leads to the suspicion of GBC. XGC can also come to light due to an acute complication of cholecystolithiasis, in particular, gallstone migration. Imaging by sonography and CT scan is suggestive, but magnetic resonance imaging is more specific. In difficult cases, biopsy may be necessary to eliminate the diagnosis of tumor. In case of pre- or intra-operative diagnostic doubt, the opinion of a hepatobiliary specialty center can be of help. When diagnosis of GBC has been eliminated, laparoscopic cholecystectomy is recommended, although with a high risk of conversion to laparotomy and complications.</description><subject>Adenocarcinoma</subject><subject>Cholecystectomy</subject><subject>Gallbladder</subject><subject>Rokitansky-Aschoff sinus</subject><subject>Xanthogranulomatous cholecystitis</subject><issn>1878-7886</issn><issn>1878-7886</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkE1PwzAMhiMEYtPYX4Aeuazko2tSOE18S5O4gMQtMqnbperHSNpJ-_dk2pi44Ytt6bVf-yHkitGYUZbeVHG1sd74wZUxp5zFlMeUJidkzJRUM6lUevqnHpGp9xUNIQSlKjsnIyFkwgRNx-TuE9p-1ZUO2qHuGui7wUdm1dVotr63vfW30YOFsu289RG0edRACyU22PYX5KyA2uP0kCfk4-nx_f5ltnx7fr1fLGdGSNbP0sLMuVGFlCJPTCFFGto5IOVcMkhASuCcCjQGE8zTPEshS1DRIgOQuVRiQq73e9eu-x7Q97oJ72NdQ4vhXM3nVCSJypgMUrmXGtd577DQa2cbcFvNqN7B05U-wtM7eJpyHeCFycuDyfDVYH6c-0UVBIu9AMOrG4tOe2OxNZhbh6bXeWf_NfkBLpqFjA</recordid><startdate>20210801</startdate><enddate>20210801</enddate><creator>Giudicelli, X.</creator><creator>Rode, A.</creator><creator>Bancel, B.</creator><creator>Nguyen, A.-T.</creator><creator>Mabrut, J.-Y.</creator><general>Elsevier Masson SAS</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20210801</creationdate><title>Xanthogranulomatous cholecystitis: Diagnosis and management</title><author>Giudicelli, X. ; Rode, A. ; Bancel, B. ; Nguyen, A.-T. ; Mabrut, J.-Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-6fc52c8f773d4cf73652c5ae02271a4a77a2203ecce4ed6d96a94e80f9aa7d783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adenocarcinoma</topic><topic>Cholecystectomy</topic><topic>Gallbladder</topic><topic>Rokitansky-Aschoff sinus</topic><topic>Xanthogranulomatous cholecystitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Giudicelli, X.</creatorcontrib><creatorcontrib>Rode, A.</creatorcontrib><creatorcontrib>Bancel, B.</creatorcontrib><creatorcontrib>Nguyen, A.-T.</creatorcontrib><creatorcontrib>Mabrut, J.-Y.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of visceral surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Giudicelli, X.</au><au>Rode, A.</au><au>Bancel, B.</au><au>Nguyen, A.-T.</au><au>Mabrut, J.-Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Xanthogranulomatous cholecystitis: Diagnosis and management</atitle><jtitle>Journal of visceral surgery</jtitle><addtitle>J Visc Surg</addtitle><date>2021-08-01</date><risdate>2021</risdate><volume>158</volume><issue>4</issue><spage>326</spage><epage>336</epage><pages>326-336</pages><issn>1878-7886</issn><eissn>1878-7886</eissn><abstract>•Xanthogranulomatous cholecystitis is a rare benign disease that can take on a pseudo-tumoral aspect.•It generally occurs in adults over 50.•Its etiopathogenesis is poorly defined.•Its association with gallbladder carcinoma remains controversial.•The best diagnostic imaging tool for xanthogranulomatous cholecystitis is magnetic resonance imaging.•Treatment is laparoscopic cholecystectomy, total or partial, with a high risk of conversion and complications.•In case of suspicion of xanthogranulomatous cholecystitis, a hepato-biliary specialty center should be involved.
Xanthogranulomatous cholecystitis (XGC) is a rare form of cholecystitis, characterized by the presence of xanthogranuloma, prominent yellow structures within the gallbladder wall that is very often lithiasic. When XGC presents in its pseudo-tumoral form with occasional adjacent organ involvement, it can mimic gallbladder carcinoma (GBC). The etiopathogenesis of XGC is inflammatory destruction of Rokitansky-Aschoff sinuses containing biliary and cholesterol pigments within the gallbladder wall; this leads to a florid granulomatous histiocytic inflammatory reaction. The prevalence ranges from 1.3% to 8.8% of all cholecystectomies and varies from country to country; XGC occurs predominantly in patients over 50 years of age, and is equally distributed between males and females. Its association with GBC remains a topic of debate in the literature (between 0 and 20%). Symptoms are non-specific and generally similar to those of acute or chronic cholecystitis. XGC, when associated with altered health status, leads to the suspicion of GBC. XGC can also come to light due to an acute complication of cholecystolithiasis, in particular, gallstone migration. Imaging by sonography and CT scan is suggestive, but magnetic resonance imaging is more specific. In difficult cases, biopsy may be necessary to eliminate the diagnosis of tumor. In case of pre- or intra-operative diagnostic doubt, the opinion of a hepatobiliary specialty center can be of help. When diagnosis of GBC has been eliminated, laparoscopic cholecystectomy is recommended, although with a high risk of conversion to laparotomy and complications.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>33741306</pmid><doi>10.1016/j.jviscsurg.2021.02.004</doi><tpages>11</tpages></addata></record> |
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subjects | Adenocarcinoma Cholecystectomy Gallbladder Rokitansky-Aschoff sinus Xanthogranulomatous cholecystitis |
title | Xanthogranulomatous cholecystitis: Diagnosis and management |
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