DIFFERENT CLINICAL PRESENTATIONS OF A RARE VENOUS MALFORMATION-INFERIOR VENA CAVA AGENESIS

Detalhes bibliográficos
Autor(a) principal: Machado, Marta
Data de Publicação: 2022
Outros Autores: Coelho, Nuno, Maximiano, Pedro, Semião, Carolina, Peixoto, João, Fernandes, Luís, Brandão, Pedro, Canedo, Alexandra
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.48750/acv.461
Resumo: INTRODUCTION: Inferior vena cava agenesis is one of the most uncommon anomalies of this vessel, with an estimated prevalence of 0.0005–1% in the general population. However, around 5% of the patients younger than 30 years with a diagnosis of deep vein thrombosis have this anomaly. METHODS AND MATERIAL: Report of two clinical cases of inferior vena cava agenesis with different clinical presentations. CLINICAL CASE 1: A 40-year-old man was admitted with a 3 days history of unilateral lower limb swelling and pain, gradually progressing to the inability to walk. On physical examination he had swelling, bruising and tenderness involving leg and thigh and prominent engorged superficial abdominal collateral veins.Venous Doppler Ultrasound showed left deep venous thrombosis extending from popliteal vein to common iliac vein. A computed tomography angiogram showed agenesis of the infrarenal vena cava and patent renal veins draining in to the azygous system and hemiazygous systems. The patient as discharged with rivaroxaban and compression stockings. At 2 months follow up he was asymptomatic and still anticoagulated. CLINICAL CASE 2: A 35 year- old woman, with a previous history of recurrent lower limb varicose veins surgery and left internal malleolar ulcer at 30 years presented at medical department 3 years later with complains of ulcer recurrence. A computed tomography angiogram revealed an absent infrahepatic vena cava, prominently dilated azygos and hemiazygos veins with enlarged retroperitoneal collaterals. The patient initiated dressing care with oxide zinc and oral rivaroxaban. DISCUSSION/CONCLUSION: The majority of cases remain asymptomatic. However, when symptomatic, the majority present as proximal DVT involving the iliac and femoral veins. CT or MRI should be the imagiological methods used to diagnose this anomaly. No clear consensus has been reached on therapeutic strategy, other than long-term antico- agulation and elastic stockings.
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spelling DIFFERENT CLINICAL PRESENTATIONS OF A RARE VENOUS MALFORMATION-INFERIOR VENA CAVA AGENESISESPETRO DE APRESENTAÇÃO CLÍNICA DE UMA MALFORMAÇÃO VENOSA RARA: AGENESIA DA VEIA CAVA INFERIORInferior Vena Cava AgenesisDeep Vein ThrombosisVascular anomaliesAgenesia da Veia Cava InferiorTrombose venosa profundaAnomalias vascularesINTRODUCTION: Inferior vena cava agenesis is one of the most uncommon anomalies of this vessel, with an estimated prevalence of 0.0005–1% in the general population. However, around 5% of the patients younger than 30 years with a diagnosis of deep vein thrombosis have this anomaly. METHODS AND MATERIAL: Report of two clinical cases of inferior vena cava agenesis with different clinical presentations. CLINICAL CASE 1: A 40-year-old man was admitted with a 3 days history of unilateral lower limb swelling and pain, gradually progressing to the inability to walk. On physical examination he had swelling, bruising and tenderness involving leg and thigh and prominent engorged superficial abdominal collateral veins.Venous Doppler Ultrasound showed left deep venous thrombosis extending from popliteal vein to common iliac vein. A computed tomography angiogram showed agenesis of the infrarenal vena cava and patent renal veins draining in to the azygous system and hemiazygous systems. The patient as discharged with rivaroxaban and compression stockings. At 2 months follow up he was asymptomatic and still anticoagulated. CLINICAL CASE 2: A 35 year- old woman, with a previous history of recurrent lower limb varicose veins surgery and left internal malleolar ulcer at 30 years presented at medical department 3 years later with complains of ulcer recurrence. A computed tomography angiogram revealed an absent infrahepatic vena cava, prominently dilated azygos and hemiazygos veins with enlarged retroperitoneal collaterals. The patient initiated dressing care with oxide zinc and oral rivaroxaban. DISCUSSION/CONCLUSION: The majority of cases remain asymptomatic. However, when symptomatic, the majority present as proximal DVT involving the iliac and femoral veins. CT or MRI should be the imagiological methods used to diagnose this anomaly. No clear consensus has been reached on therapeutic strategy, other than long-term antico- agulation and elastic stockings.INTRODUÇÃO: A agenesia da veia cava inferior é uma das anomalias mais raras deste vaso, com uma prevalência esti- mada de 0,0005–1% na população geral. Porém, cerca de 5% dos pacientes com menos de 30 anos com uma trombose venosa profunda apresentam esta anomalia. MÉTODOS E MATERIAL: Relato de dois casos clínicos de agenesia da veia cava inferior com diferentes apresenta- ções clínicas. CASO CLÍNICO 1: Um homem de 40 anos recorreu à urgência com queixas de edema e dor no membro inferior esquerdo, progredindo gradualmente para incapacidade de marcha. Ao exame físico foi encontrado edema e dor a palpação da perna e coxa, bem como veias colaterais abdominais superficiais proeminentes.O ecodoppler venoso mostrou trombose venosa profunda esquerda estendendo-se da veia poplítea até a veia ilíaca comum. O angio-TC mostrou agenesia da veia cava infrarrenal e veias renais a drenar para os sistemas ázigos e hemiázigos. O paciente teve alta com rivaroxabano e meias elásticas. Aos 2 meses mantinha-se hipocoagulado e estava assintomático. CASO CLÍNICO 2: Uma mulher de 35 anos, com história prévia de cirurgia de varizes de membros inferiores recorrentes e úlcera do maléolo interno esquerdo, apresentou-se na consulta com recorrência da úlcera.O angio-TC revelou ausência de veia cava infra-hepática, veias ázigos e hemiázigos dilatadas com colaterais retro- peritoneais dilatadas. A paciente iniciou cuidados de penso com óxido de zinco e rivaroxabano oral. DISCUSSÃO / CONCLUSÃO: A maioria dos pacientes com agenesia da veia cava inferior permanece assintomática. No entanto, quando sintomática, a maioria apresenta-se com uma trombose venosa profunda proximal envolvendo as veias ilíaca e femoral. A TC ou RM devem ser os métodos imagiológicos usados para diagnosticar esta anomalia. Nenhum consenso claro foi alcançado sobre a estratégia terapêutica, além da anticoagulação de longo prazo e uso de meias elásticas.Sociedade Portuguesa de Angiologia e Cirurgia Vascular2022-03-02T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.48750/acv.461oai:ojs.acvjournal.com:article/461Angiologia e Cirurgia Vascular; Vol. 17 No. 4 (2021): December; 325-329Angiologia e Cirurgia Vascular; Vol. 17 N.º 4 (2021): Dezembro; 325-3292183-00961646-706Xreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttp://acvjournal.com/index.php/acv/article/view/461https://doi.org/10.48750/acv.461http://acvjournal.com/index.php/acv/article/view/461/274Copyright (c) 2022 Angiologia e Cirurgia Vascularinfo:eu-repo/semantics/openAccessMachado, MartaCoelho, NunoMaximiano, PedroSemião, CarolinaPeixoto, JoãoFernandes, LuísBrandão, PedroCanedo, Alexandra2022-05-23T15:10:14Zoai:ojs.acvjournal.com:article/461Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T14:57:46.681300Repositório 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 DIFFERENT CLINICAL PRESENTATIONS OF A RARE VENOUS MALFORMATION-INFERIOR VENA CAVA AGENESIS
ESPETRO DE APRESENTAÇÃO CLÍNICA DE UMA MALFORMAÇÃO VENOSA RARA: AGENESIA DA VEIA CAVA INFERIOR
title DIFFERENT CLINICAL PRESENTATIONS OF A RARE VENOUS MALFORMATION-INFERIOR VENA CAVA AGENESIS
spellingShingle DIFFERENT CLINICAL PRESENTATIONS OF A RARE VENOUS MALFORMATION-INFERIOR VENA CAVA AGENESIS
Machado, Marta
Inferior Vena Cava Agenesis
Deep Vein Thrombosis
Vascular anomalies
Agenesia da Veia Cava Inferior
Trombose venosa profunda
Anomalias vasculares
title_short DIFFERENT CLINICAL PRESENTATIONS OF A RARE VENOUS MALFORMATION-INFERIOR VENA CAVA AGENESIS
title_full DIFFERENT CLINICAL PRESENTATIONS OF A RARE VENOUS MALFORMATION-INFERIOR VENA CAVA AGENESIS
title_fullStr DIFFERENT CLINICAL PRESENTATIONS OF A RARE VENOUS MALFORMATION-INFERIOR VENA CAVA AGENESIS
title_full_unstemmed DIFFERENT CLINICAL PRESENTATIONS OF A RARE VENOUS MALFORMATION-INFERIOR VENA CAVA AGENESIS
title_sort DIFFERENT CLINICAL PRESENTATIONS OF A RARE VENOUS MALFORMATION-INFERIOR VENA CAVA AGENESIS
author Machado, Marta
author_facet Machado, Marta
Coelho, Nuno
Maximiano, Pedro
Semião, Carolina
Peixoto, João
Fernandes, Luís
Brandão, Pedro
Canedo, Alexandra
author_role author
author2 Coelho, Nuno
Maximiano, Pedro
Semião, Carolina
Peixoto, João
Fernandes, Luís
Brandão, Pedro
Canedo, Alexandra
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Machado, Marta
Coelho, Nuno
Maximiano, Pedro
Semião, Carolina
Peixoto, João
Fernandes, Luís
Brandão, Pedro
Canedo, Alexandra
dc.subject.por.fl_str_mv Inferior Vena Cava Agenesis
Deep Vein Thrombosis
Vascular anomalies
Agenesia da Veia Cava Inferior
Trombose venosa profunda
Anomalias vasculares
topic Inferior Vena Cava Agenesis
Deep Vein Thrombosis
Vascular anomalies
Agenesia da Veia Cava Inferior
Trombose venosa profunda
Anomalias vasculares
description INTRODUCTION: Inferior vena cava agenesis is one of the most uncommon anomalies of this vessel, with an estimated prevalence of 0.0005–1% in the general population. However, around 5% of the patients younger than 30 years with a diagnosis of deep vein thrombosis have this anomaly. METHODS AND MATERIAL: Report of two clinical cases of inferior vena cava agenesis with different clinical presentations. CLINICAL CASE 1: A 40-year-old man was admitted with a 3 days history of unilateral lower limb swelling and pain, gradually progressing to the inability to walk. On physical examination he had swelling, bruising and tenderness involving leg and thigh and prominent engorged superficial abdominal collateral veins.Venous Doppler Ultrasound showed left deep venous thrombosis extending from popliteal vein to common iliac vein. A computed tomography angiogram showed agenesis of the infrarenal vena cava and patent renal veins draining in to the azygous system and hemiazygous systems. The patient as discharged with rivaroxaban and compression stockings. At 2 months follow up he was asymptomatic and still anticoagulated. CLINICAL CASE 2: A 35 year- old woman, with a previous history of recurrent lower limb varicose veins surgery and left internal malleolar ulcer at 30 years presented at medical department 3 years later with complains of ulcer recurrence. A computed tomography angiogram revealed an absent infrahepatic vena cava, prominently dilated azygos and hemiazygos veins with enlarged retroperitoneal collaterals. The patient initiated dressing care with oxide zinc and oral rivaroxaban. DISCUSSION/CONCLUSION: The majority of cases remain asymptomatic. However, when symptomatic, the majority present as proximal DVT involving the iliac and femoral veins. CT or MRI should be the imagiological methods used to diagnose this anomaly. No clear consensus has been reached on therapeutic strategy, other than long-term antico- agulation and elastic stockings.
publishDate 2022
dc.date.none.fl_str_mv 2022-03-02T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://doi.org/10.48750/acv.461
oai:ojs.acvjournal.com:article/461
url https://doi.org/10.48750/acv.461
identifier_str_mv oai:ojs.acvjournal.com:article/461
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv http://acvjournal.com/index.php/acv/article/view/461
https://doi.org/10.48750/acv.461
http://acvjournal.com/index.php/acv/article/view/461/274
dc.rights.driver.fl_str_mv Copyright (c) 2022 Angiologia e Cirurgia Vascular
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2022 Angiologia e Cirurgia Vascular
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Sociedade Portuguesa de Angiologia e Cirurgia Vascular
publisher.none.fl_str_mv Sociedade Portuguesa de Angiologia e Cirurgia Vascular
dc.source.none.fl_str_mv Angiologia e Cirurgia Vascular; Vol. 17 No. 4 (2021): December; 325-329
Angiologia e Cirurgia Vascular; Vol. 17 N.º 4 (2021): Dezembro; 325-329
2183-0096
1646-706X
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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