CLINICAL APPROACH IN MIRIZZI SYNDROME: A RETROSPECTIVE COMPARATIVE STUDY

Detalhes bibliográficos
Autor(a) principal: Correia, Paulo Costa
Data de Publicação: 2023
Outros Autores: Coutinho, Liliana, Caldes, Pedro, Vale, Maria João
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.34635/rpc.875
Resumo: Introduction: The Mirizzi syndrome consists of the obstruction either of the common hepatic duct or the choledocus, secondary to the impact of calculus in the cystic duct or in the gallbladder infundibulum. According to the Csendes classification, Mirizzi syndrome is divided into five types that involve different surgical procedures. Materials and methods: After a literature review, fifteen patients with Mirizzi Syndrome are retrospectively described between 2008 and 2018 at the Unidade Saude da Guarda (ULSG). The clinical records were reviewed. Clinical data, gender, clinical condition, test results, operative procedures and type of Mirizzi syndrome (according to Csendes) were examined. Results: Of the 15 patients, 11 (73,3%) were women and 4 (26,7%) men. All of them (100%) showed abdominal pain, 14 (93,3%) nausea and vomit, 10 (66,7%) symptoms of cholangitis / acute cholecystitis, 5 (33%) recurrent jaundice, 4 (26,6%) choluria and weight loss and 2 (13,3%) itch. Every cases of Mirizzi syndrome was diagnosed intraoperatively and requiring conversion to laparotomy. Were identified 5(33,3%) cases with type III, 4 (26,6%) with type I, 3 (20%) with type II, 2 (13,3%) with type IV and 1 (6,7%) with type V. In 5 (33,3%) patients was treated with cholecystectomy and bilio-digestive anastomosis on Roux-en-Y, 3 (20%) by total cholecystectomy with Kher drain, 2 (13,3%) by total cholecystectomy, partial and partial with Kher drain, and finally 1 (6,6%) by cholecystectomy with Kher drain with suture of the gastric orifice. Conclusion: The treatment of Mirizzi Syndrome is a diagnosis and surgical challenge. Despite the era of laparoscopic cholecystectomy, the laparotomic treatment of Mirizzi syndrome should be the standard procedure.
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spelling CLINICAL APPROACH IN MIRIZZI SYNDROME: A RETROSPECTIVE COMPARATIVE STUDYABORDAGEM CLÍNICA NA SÍNDROME DE MIRIZZI: ANÁLISE RETROSPETIVAIntroduction: The Mirizzi syndrome consists of the obstruction either of the common hepatic duct or the choledocus, secondary to the impact of calculus in the cystic duct or in the gallbladder infundibulum. According to the Csendes classification, Mirizzi syndrome is divided into five types that involve different surgical procedures. Materials and methods: After a literature review, fifteen patients with Mirizzi Syndrome are retrospectively described between 2008 and 2018 at the Unidade Saude da Guarda (ULSG). The clinical records were reviewed. Clinical data, gender, clinical condition, test results, operative procedures and type of Mirizzi syndrome (according to Csendes) were examined. Results: Of the 15 patients, 11 (73,3%) were women and 4 (26,7%) men. All of them (100%) showed abdominal pain, 14 (93,3%) nausea and vomit, 10 (66,7%) symptoms of cholangitis / acute cholecystitis, 5 (33%) recurrent jaundice, 4 (26,6%) choluria and weight loss and 2 (13,3%) itch. Every cases of Mirizzi syndrome was diagnosed intraoperatively and requiring conversion to laparotomy. Were identified 5(33,3%) cases with type III, 4 (26,6%) with type I, 3 (20%) with type II, 2 (13,3%) with type IV and 1 (6,7%) with type V. In 5 (33,3%) patients was treated with cholecystectomy and bilio-digestive anastomosis on Roux-en-Y, 3 (20%) by total cholecystectomy with Kher drain, 2 (13,3%) by total cholecystectomy, partial and partial with Kher drain, and finally 1 (6,6%) by cholecystectomy with Kher drain with suture of the gastric orifice. Conclusion: The treatment of Mirizzi Syndrome is a diagnosis and surgical challenge. Despite the era of laparoscopic cholecystectomy, the laparotomic treatment of Mirizzi syndrome should be the standard procedure.Introdução: A Síndrome de Mirizzi resulta da compressão extrínseca do canal hepático comum (CHC) e/ou colédoco pela impactação de cálculos no canal cístico ou no infundíbulo da vesícula biliar. Segundo a classificação de Csendes, dividide-se em 5 tipos que implicam diferentes técnicas cirúrgicas. Materiais e Métodos: Após uma breve revisão bibliográfica, descrevem-se retrospetivamente quinze doentes diagnosticados com Síndrome de Mirizzi, entre 2008 e 2018, na Unidade Local de Saúde da Guarda (ULSG). A análise dos respectivos processos clínicos permitiu recolher dados relativamente ao género, quadro clínico, resultados de exames complementares de diagnóstico, momento do diagnóstico, tipo de síndrome de Mirizzi (segundo Csendes) e tratamento cirúrgico. Resultados: Dos 15 doentes, 11 (73,3%) eram mulheres e 4 (26,7%) homens. Todos os doentes (100%) apresentaram dor abdominal, 14 (93,3%) náuseas e vómitos, 10 (66,7%) sintomas de colangite/colecistite aguda, 5 (33%) icterícia recorrente, 4 (26,6%) colúria e emagrecimento e 2 (13,3%) prurido. O diagnóstico foi estabelecido, em todos os casos, intra-operatoriamente com necessidade de conversão para laparotomia, sendo: 5 (33,3%) do tipo III, 4 (26,6%) do tipo I, 3 (20%) do tipo II, 2 (13,3%) do tipo IV e 1 (6,7%) do tipo V. Foi realizada em 5 (33,3%) doentes colecistectomia com anastomose bilio-digestiva em Y de Roux, em 3 (20%) colecistectomia total com dreno de Kehr, em 2 (13,3%) colecistectomia total, parcial e parcial com dreno de Kehr e por fim, em 1 (6,6%) colecistectomia com dreno de Kehr com sutura de orifício gástrico. Conclusões: O tratamento da Síndrome de Mirizzi é um desafio diagnóstico e cirúrgico. Apesar da era da colecistectomia laparoscópica, a via laparotómica deve ser a via de abordagem de eleição para o tratamento cirúrgico desta entidade.Sociedade Portuguesa de Cirurgia2023-03-18info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.34635/rpc.875https://doi.org/10.34635/rpc.875Revista Portuguesa de Cirurgia; No 54 (2022): December; 55-61Revista Portuguesa de Cirurgia; No 54 (2022): December; 55-612183-11651646-6918reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPporhttps://revista.spcir.com/index.php/spcir/article/view/875https://revista.spcir.com/index.php/spcir/article/view/875/663Copyright (c) 2023 Revista Portuguesa de Cirurgiainfo:eu-repo/semantics/openAccessCorreia, Paulo CostaCoutinho, LilianaCaldes, PedroVale, Maria João2024-03-14T22:04:48Zoai:revista.spcir.com:article/875Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T04:00:43.981735Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv CLINICAL APPROACH IN MIRIZZI SYNDROME: A RETROSPECTIVE COMPARATIVE STUDY
ABORDAGEM CLÍNICA NA SÍNDROME DE MIRIZZI: ANÁLISE RETROSPETIVA
title CLINICAL APPROACH IN MIRIZZI SYNDROME: A RETROSPECTIVE COMPARATIVE STUDY
spellingShingle CLINICAL APPROACH IN MIRIZZI SYNDROME: A RETROSPECTIVE COMPARATIVE STUDY
Correia, Paulo Costa
title_short CLINICAL APPROACH IN MIRIZZI SYNDROME: A RETROSPECTIVE COMPARATIVE STUDY
title_full CLINICAL APPROACH IN MIRIZZI SYNDROME: A RETROSPECTIVE COMPARATIVE STUDY
title_fullStr CLINICAL APPROACH IN MIRIZZI SYNDROME: A RETROSPECTIVE COMPARATIVE STUDY
title_full_unstemmed CLINICAL APPROACH IN MIRIZZI SYNDROME: A RETROSPECTIVE COMPARATIVE STUDY
title_sort CLINICAL APPROACH IN MIRIZZI SYNDROME: A RETROSPECTIVE COMPARATIVE STUDY
author Correia, Paulo Costa
author_facet Correia, Paulo Costa
Coutinho, Liliana
Caldes, Pedro
Vale, Maria João
author_role author
author2 Coutinho, Liliana
Caldes, Pedro
Vale, Maria João
author2_role author
author
author
dc.contributor.author.fl_str_mv Correia, Paulo Costa
Coutinho, Liliana
Caldes, Pedro
Vale, Maria João
description Introduction: The Mirizzi syndrome consists of the obstruction either of the common hepatic duct or the choledocus, secondary to the impact of calculus in the cystic duct or in the gallbladder infundibulum. According to the Csendes classification, Mirizzi syndrome is divided into five types that involve different surgical procedures. Materials and methods: After a literature review, fifteen patients with Mirizzi Syndrome are retrospectively described between 2008 and 2018 at the Unidade Saude da Guarda (ULSG). The clinical records were reviewed. Clinical data, gender, clinical condition, test results, operative procedures and type of Mirizzi syndrome (according to Csendes) were examined. Results: Of the 15 patients, 11 (73,3%) were women and 4 (26,7%) men. All of them (100%) showed abdominal pain, 14 (93,3%) nausea and vomit, 10 (66,7%) symptoms of cholangitis / acute cholecystitis, 5 (33%) recurrent jaundice, 4 (26,6%) choluria and weight loss and 2 (13,3%) itch. Every cases of Mirizzi syndrome was diagnosed intraoperatively and requiring conversion to laparotomy. Were identified 5(33,3%) cases with type III, 4 (26,6%) with type I, 3 (20%) with type II, 2 (13,3%) with type IV and 1 (6,7%) with type V. In 5 (33,3%) patients was treated with cholecystectomy and bilio-digestive anastomosis on Roux-en-Y, 3 (20%) by total cholecystectomy with Kher drain, 2 (13,3%) by total cholecystectomy, partial and partial with Kher drain, and finally 1 (6,6%) by cholecystectomy with Kher drain with suture of the gastric orifice. Conclusion: The treatment of Mirizzi Syndrome is a diagnosis and surgical challenge. Despite the era of laparoscopic cholecystectomy, the laparotomic treatment of Mirizzi syndrome should be the standard procedure.
publishDate 2023
dc.date.none.fl_str_mv 2023-03-18
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dc.language.iso.fl_str_mv por
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dc.relation.none.fl_str_mv https://revista.spcir.com/index.php/spcir/article/view/875
https://revista.spcir.com/index.php/spcir/article/view/875/663
dc.rights.driver.fl_str_mv Copyright (c) 2023 Revista Portuguesa de Cirurgia
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dc.publisher.none.fl_str_mv Sociedade Portuguesa de Cirurgia
publisher.none.fl_str_mv Sociedade Portuguesa de Cirurgia
dc.source.none.fl_str_mv Revista Portuguesa de Cirurgia; No 54 (2022): December; 55-61
Revista Portuguesa de Cirurgia; No 54 (2022): December; 55-61
2183-1165
1646-6918
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