Loading…
Mirizzi Syndrome Type IV: A challenging diagnosis
Mirizzi Syndrome type IV is an extremely rare condition, which is confused with the diagnosis of cholangiocarcinoma in many cases. This report describes a case of a forty-three-year old patient, who was forwarded to our department of general surgery with a high suspicion of a choledochal neoplasic l...
Saved in:
Published in: | Clinical and Biomedical Research 2016-05, Vol.36 (1) |
---|---|
Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | |
container_issue | 1 |
container_start_page | |
container_title | Clinical and Biomedical Research |
container_volume | 36 |
creator | Daniel Navarini Carlos Augusto Scussel Madalosso Diego Reffatti Luma Guareschi Ana Paula Schmitt Guilherme Marx Paula Jaskulski Henrique Ribeiro Thalis Laydner |
description | Mirizzi Syndrome type IV is an extremely rare condition, which is confused with the diagnosis of cholangiocarcinoma in many cases. This report describes a case of a forty-three-year old patient, who was forwarded to our department of general surgery with a high suspicion of a choledochal neoplasic lesion. During the hospitalization he was diagnosed with Mirizzi Syndrome type IV. We concisely describe the case and the literature review about this pathology. |
format | article |
fullrecord | <record><control><sourceid>doaj</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_782d6a978ddd4080b1f11ebcd247ad2d</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_782d6a978ddd4080b1f11ebcd247ad2d</doaj_id><sourcerecordid>oai_doaj_org_article_782d6a978ddd4080b1f11ebcd247ad2d</sourcerecordid><originalsourceid>FETCH-doaj_primary_oai_doaj_org_article_782d6a978ddd4080b1f11ebcd247ad2d3</originalsourceid><addsrcrecordid>eNqtzE0KwjAQQOEgChb1DrlAIUl_0roTUezClcVtmHbSOlIbSdzU0wviEVw9-BZvxiKVZDoudSLmLBJSyDjLdLZkmxCoEbLQIslVGTF5Jk_vN_HLNKJ3D8vr6Wl5dd3yHW9vMAx27GnsORL0owsU1mzRwRDs5tcVq46Hen-K0cHdPD09wE_GAZkvON8b8C9qB2t0oTCHUheImIpCNLKT0jYtqlQDKkz--foAVZBP6A</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Mirizzi Syndrome Type IV: A challenging diagnosis</title><source>Alma/SFX Local Collection</source><creator>Daniel Navarini ; Carlos Augusto Scussel Madalosso ; Diego Reffatti ; Luma Guareschi ; Ana Paula Schmitt ; Guilherme Marx ; Paula Jaskulski ; Henrique Ribeiro ; Thalis Laydner</creator><creatorcontrib>Daniel Navarini ; Carlos Augusto Scussel Madalosso ; Diego Reffatti ; Luma Guareschi ; Ana Paula Schmitt ; Guilherme Marx ; Paula Jaskulski ; Henrique Ribeiro ; Thalis Laydner</creatorcontrib><description>Mirizzi Syndrome type IV is an extremely rare condition, which is confused with the diagnosis of cholangiocarcinoma in many cases. This report describes a case of a forty-three-year old patient, who was forwarded to our department of general surgery with a high suspicion of a choledochal neoplasic lesion. During the hospitalization he was diagnosed with Mirizzi Syndrome type IV. We concisely describe the case and the literature review about this pathology.</description><identifier>ISSN: 0101-5575</identifier><identifier>EISSN: 2357-9730</identifier><language>eng</language><publisher>Hospital de Clinicas de Porto Alegre ; Universidade Federal do Rio Grande do Sul (UFRGS)</publisher><subject>cholangiocarcinoma ; jaundice ; Mirizzi Syndrome</subject><ispartof>Clinical and Biomedical Research, 2016-05, Vol.36 (1)</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781</link.rule.ids></links><search><creatorcontrib>Daniel Navarini</creatorcontrib><creatorcontrib>Carlos Augusto Scussel Madalosso</creatorcontrib><creatorcontrib>Diego Reffatti</creatorcontrib><creatorcontrib>Luma Guareschi</creatorcontrib><creatorcontrib>Ana Paula Schmitt</creatorcontrib><creatorcontrib>Guilherme Marx</creatorcontrib><creatorcontrib>Paula Jaskulski</creatorcontrib><creatorcontrib>Henrique Ribeiro</creatorcontrib><creatorcontrib>Thalis Laydner</creatorcontrib><title>Mirizzi Syndrome Type IV: A challenging diagnosis</title><title>Clinical and Biomedical Research</title><description>Mirizzi Syndrome type IV is an extremely rare condition, which is confused with the diagnosis of cholangiocarcinoma in many cases. This report describes a case of a forty-three-year old patient, who was forwarded to our department of general surgery with a high suspicion of a choledochal neoplasic lesion. During the hospitalization he was diagnosed with Mirizzi Syndrome type IV. We concisely describe the case and the literature review about this pathology.</description><subject>cholangiocarcinoma</subject><subject>jaundice</subject><subject>Mirizzi Syndrome</subject><issn>0101-5575</issn><issn>2357-9730</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNqtzE0KwjAQQOEgChb1DrlAIUl_0roTUezClcVtmHbSOlIbSdzU0wviEVw9-BZvxiKVZDoudSLmLBJSyDjLdLZkmxCoEbLQIslVGTF5Jk_vN_HLNKJ3D8vr6Wl5dd3yHW9vMAx27GnsORL0owsU1mzRwRDs5tcVq46Hen-K0cHdPD09wE_GAZkvON8b8C9qB2t0oTCHUheImIpCNLKT0jYtqlQDKkz--foAVZBP6A</recordid><startdate>20160501</startdate><enddate>20160501</enddate><creator>Daniel Navarini</creator><creator>Carlos Augusto Scussel Madalosso</creator><creator>Diego Reffatti</creator><creator>Luma Guareschi</creator><creator>Ana Paula Schmitt</creator><creator>Guilherme Marx</creator><creator>Paula Jaskulski</creator><creator>Henrique Ribeiro</creator><creator>Thalis Laydner</creator><general>Hospital de Clinicas de Porto Alegre ; Universidade Federal do Rio Grande do Sul (UFRGS)</general><scope>DOA</scope></search><sort><creationdate>20160501</creationdate><title>Mirizzi Syndrome Type IV: A challenging diagnosis</title><author>Daniel Navarini ; Carlos Augusto Scussel Madalosso ; Diego Reffatti ; Luma Guareschi ; Ana Paula Schmitt ; Guilherme Marx ; Paula Jaskulski ; Henrique Ribeiro ; Thalis Laydner</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-doaj_primary_oai_doaj_org_article_782d6a978ddd4080b1f11ebcd247ad2d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>cholangiocarcinoma</topic><topic>jaundice</topic><topic>Mirizzi Syndrome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Daniel Navarini</creatorcontrib><creatorcontrib>Carlos Augusto Scussel Madalosso</creatorcontrib><creatorcontrib>Diego Reffatti</creatorcontrib><creatorcontrib>Luma Guareschi</creatorcontrib><creatorcontrib>Ana Paula Schmitt</creatorcontrib><creatorcontrib>Guilherme Marx</creatorcontrib><creatorcontrib>Paula Jaskulski</creatorcontrib><creatorcontrib>Henrique Ribeiro</creatorcontrib><creatorcontrib>Thalis Laydner</creatorcontrib><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Clinical and Biomedical Research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Daniel Navarini</au><au>Carlos Augusto Scussel Madalosso</au><au>Diego Reffatti</au><au>Luma Guareschi</au><au>Ana Paula Schmitt</au><au>Guilherme Marx</au><au>Paula Jaskulski</au><au>Henrique Ribeiro</au><au>Thalis Laydner</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mirizzi Syndrome Type IV: A challenging diagnosis</atitle><jtitle>Clinical and Biomedical Research</jtitle><date>2016-05-01</date><risdate>2016</risdate><volume>36</volume><issue>1</issue><issn>0101-5575</issn><eissn>2357-9730</eissn><abstract>Mirizzi Syndrome type IV is an extremely rare condition, which is confused with the diagnosis of cholangiocarcinoma in many cases. This report describes a case of a forty-three-year old patient, who was forwarded to our department of general surgery with a high suspicion of a choledochal neoplasic lesion. During the hospitalization he was diagnosed with Mirizzi Syndrome type IV. We concisely describe the case and the literature review about this pathology.</abstract><pub>Hospital de Clinicas de Porto Alegre ; Universidade Federal do Rio Grande do Sul (UFRGS)</pub><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0101-5575 |
ispartof | Clinical and Biomedical Research, 2016-05, Vol.36 (1) |
issn | 0101-5575 2357-9730 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_782d6a978ddd4080b1f11ebcd247ad2d |
source | Alma/SFX Local Collection |
subjects | cholangiocarcinoma jaundice Mirizzi Syndrome |
title | Mirizzi Syndrome Type IV: A challenging diagnosis |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T05%3A28%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-doaj&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Mirizzi%20Syndrome%20Type%20IV:%20A%20challenging%20diagnosis&rft.jtitle=Clinical%20and%20Biomedical%20Research&rft.au=Daniel%20Navarini&rft.date=2016-05-01&rft.volume=36&rft.issue=1&rft.issn=0101-5575&rft.eissn=2357-9730&rft_id=info:doi/&rft_dat=%3Cdoaj%3Eoai_doaj_org_article_782d6a978ddd4080b1f11ebcd247ad2d%3C/doaj%3E%3Cgrp_id%3Ecdi_FETCH-doaj_primary_oai_doaj_org_article_782d6a978ddd4080b1f11ebcd247ad2d3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |