Left-Sided Portal Hypertension: A Sinister Entity

Detalhes bibliográficos
Autor(a) principal: Fernandes, Alexandra
Data de Publicação: 2015
Outros Autores: Almeida, Nuno, Ferreira, Ana Margarida, Casela, Adriano, Gomes, Dário, Portela, Francisco, Camacho, Ernestina, Sofia, Carlos
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/109160
https://doi.org/10.1016/j.jpge.2015.09.006
Resumo: Introduction: Sinistral, or left-sided, portal hypertension (SPH) is a rare entity, with multiple potential causes. Gastrointestinal variceal bleeding and hypersplenism are its’ major clinical manifestations. The main aim of the present study is to summarize the clinical features of patients with SPH. Patients and methods: This was a retrospective analysis of consecutive patients with present or previous diagnosis of SHP, observed in a Gastroenterology Department, in a period of 2 years. Patients with clinical, radiological or laboratory alterations suggestive of cirrhosis were excluded. Causes of SPH, clinical manifestations and outcomes were registered. Potential factors associated with gastrointestinal bleeding were analyzed. Results: In the study period a total of 22 patients (male --- 17; mean age --- 59.6 ± 10.6 years) with SHP were included. Clinical manifestations were: asymptomatic/unspecific abdominal pain (n = 14); gastrointestinal bleeding (n = 8). Eleven (50%) patients had increased aminotransferases, GGT and/or alkaline phosphatase although liver function was normal in all of them. Causes of SPH were chronic pancreatitis (n = 7), acute pancreatitis (n = 7), pancreatic cancer (n = 4), pancreatic surgery (n = 3) and arteriovenous malformation (n = 1). All patients had gastric and/or esophageal varices and seven had splenomegaly. Five (22.7%) had thrombocytopenia, associated with hypersplenism. Five patients (22.7%) were submitted to endoscopic treatment and eight were submitted to splenic artery embolization and/or splenectomy. There were no cases of variceal rebleeding and two patients died. Patients without liver enzymes elevation had a higher probability of gastrointestinal bleeding (87.5% vs. 28.6%; p = 0.024). Conclusions: Acute and chronic pancreatitis are the major causes of SHP. Gastrointestinal bleeding is the most important clinical manifestation and patients without liver enzyme elevation seem more prone to bleed. Specific treatment is seldom performed or needed.
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spelling Left-Sided Portal Hypertension: A Sinister EntityHypertension PortalEsophageal and Gastric VaricesPancreatitisPancreatic NeoplasmsIntroduction: Sinistral, or left-sided, portal hypertension (SPH) is a rare entity, with multiple potential causes. Gastrointestinal variceal bleeding and hypersplenism are its’ major clinical manifestations. The main aim of the present study is to summarize the clinical features of patients with SPH. Patients and methods: This was a retrospective analysis of consecutive patients with present or previous diagnosis of SHP, observed in a Gastroenterology Department, in a period of 2 years. Patients with clinical, radiological or laboratory alterations suggestive of cirrhosis were excluded. Causes of SPH, clinical manifestations and outcomes were registered. Potential factors associated with gastrointestinal bleeding were analyzed. Results: In the study period a total of 22 patients (male --- 17; mean age --- 59.6 ± 10.6 years) with SHP were included. Clinical manifestations were: asymptomatic/unspecific abdominal pain (n = 14); gastrointestinal bleeding (n = 8). Eleven (50%) patients had increased aminotransferases, GGT and/or alkaline phosphatase although liver function was normal in all of them. Causes of SPH were chronic pancreatitis (n = 7), acute pancreatitis (n = 7), pancreatic cancer (n = 4), pancreatic surgery (n = 3) and arteriovenous malformation (n = 1). All patients had gastric and/or esophageal varices and seven had splenomegaly. Five (22.7%) had thrombocytopenia, associated with hypersplenism. Five patients (22.7%) were submitted to endoscopic treatment and eight were submitted to splenic artery embolization and/or splenectomy. There were no cases of variceal rebleeding and two patients died. Patients without liver enzymes elevation had a higher probability of gastrointestinal bleeding (87.5% vs. 28.6%; p = 0.024). Conclusions: Acute and chronic pancreatitis are the major causes of SHP. Gastrointestinal bleeding is the most important clinical manifestation and patients without liver enzyme elevation seem more prone to bleed. Specific treatment is seldom performed or needed.Elsevier2015info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/109160http://hdl.handle.net/10316/109160https://doi.org/10.1016/j.jpge.2015.09.006eng2341-4545Fernandes, AlexandraAlmeida, NunoFerreira, Ana MargaridaCasela, AdrianoGomes, DárioPortela, FranciscoCamacho, ErnestinaSofia, Carlosinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-09-29T09:36:56Zoai:estudogeral.uc.pt:10316/109160Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:25:21.471757Repositório 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 Left-Sided Portal Hypertension: A Sinister Entity
title Left-Sided Portal Hypertension: A Sinister Entity
spellingShingle Left-Sided Portal Hypertension: A Sinister Entity
Fernandes, Alexandra
Hypertension Portal
Esophageal and Gastric Varices
Pancreatitis
Pancreatic Neoplasms
title_short Left-Sided Portal Hypertension: A Sinister Entity
title_full Left-Sided Portal Hypertension: A Sinister Entity
title_fullStr Left-Sided Portal Hypertension: A Sinister Entity
title_full_unstemmed Left-Sided Portal Hypertension: A Sinister Entity
title_sort Left-Sided Portal Hypertension: A Sinister Entity
author Fernandes, Alexandra
author_facet Fernandes, Alexandra
Almeida, Nuno
Ferreira, Ana Margarida
Casela, Adriano
Gomes, Dário
Portela, Francisco
Camacho, Ernestina
Sofia, Carlos
author_role author
author2 Almeida, Nuno
Ferreira, Ana Margarida
Casela, Adriano
Gomes, Dário
Portela, Francisco
Camacho, Ernestina
Sofia, Carlos
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Fernandes, Alexandra
Almeida, Nuno
Ferreira, Ana Margarida
Casela, Adriano
Gomes, Dário
Portela, Francisco
Camacho, Ernestina
Sofia, Carlos
dc.subject.por.fl_str_mv Hypertension Portal
Esophageal and Gastric Varices
Pancreatitis
Pancreatic Neoplasms
topic Hypertension Portal
Esophageal and Gastric Varices
Pancreatitis
Pancreatic Neoplasms
description Introduction: Sinistral, or left-sided, portal hypertension (SPH) is a rare entity, with multiple potential causes. Gastrointestinal variceal bleeding and hypersplenism are its’ major clinical manifestations. The main aim of the present study is to summarize the clinical features of patients with SPH. Patients and methods: This was a retrospective analysis of consecutive patients with present or previous diagnosis of SHP, observed in a Gastroenterology Department, in a period of 2 years. Patients with clinical, radiological or laboratory alterations suggestive of cirrhosis were excluded. Causes of SPH, clinical manifestations and outcomes were registered. Potential factors associated with gastrointestinal bleeding were analyzed. Results: In the study period a total of 22 patients (male --- 17; mean age --- 59.6 ± 10.6 years) with SHP were included. Clinical manifestations were: asymptomatic/unspecific abdominal pain (n = 14); gastrointestinal bleeding (n = 8). Eleven (50%) patients had increased aminotransferases, GGT and/or alkaline phosphatase although liver function was normal in all of them. Causes of SPH were chronic pancreatitis (n = 7), acute pancreatitis (n = 7), pancreatic cancer (n = 4), pancreatic surgery (n = 3) and arteriovenous malformation (n = 1). All patients had gastric and/or esophageal varices and seven had splenomegaly. Five (22.7%) had thrombocytopenia, associated with hypersplenism. Five patients (22.7%) were submitted to endoscopic treatment and eight were submitted to splenic artery embolization and/or splenectomy. There were no cases of variceal rebleeding and two patients died. Patients without liver enzymes elevation had a higher probability of gastrointestinal bleeding (87.5% vs. 28.6%; p = 0.024). Conclusions: Acute and chronic pancreatitis are the major causes of SHP. Gastrointestinal bleeding is the most important clinical manifestation and patients without liver enzyme elevation seem more prone to bleed. Specific treatment is seldom performed or needed.
publishDate 2015
dc.date.none.fl_str_mv 2015
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/109160
http://hdl.handle.net/10316/109160
https://doi.org/10.1016/j.jpge.2015.09.006
url http://hdl.handle.net/10316/109160
https://doi.org/10.1016/j.jpge.2015.09.006
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