Raras
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Malformação arteriovenosa pulmonar
ORPHA:2038CID-10 · Q25.7CID-11 · LA90.5OMIM 265140DOENÇA RARA

OBSOLETO. A malformação arteriovenosa pulmonar (MAVP) descreve uma comunicação anatômica entre uma artéria pulmonar e uma veia pulmonar levando a um shunt extracardíaco direito-esquerdo que pode ser assintomático ou levar a manifestações variadas, como dispneia, hemoptise e sintomas neurológicos.

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Introdução

O que você precisa saber de cara

📋

OBSOLETO. A malformação arteriovenosa pulmonar (MAVP) descreve uma comunicação anatômica entre uma artéria pulmonar e uma veia pulmonar levando a um shunt extracardíaco direito-esquerdo que pode ser assintomático ou levar a manifestações variadas, como dispneia, hemoptise e sintomas neurológicos.

Pesquisas ativas
4 ensaios
11 total registrados no ClinicalTrials.gov
Publicações científicas
840 artigos
Último publicado: 2026 Apr 15

Escala de raridade

CLASSIFICAÇÃO ORPHANET · BRASIL 2024
Unknown
Ultra-rara
<1/50k
Muito rara
1/20k
Rara
1/10k
Pouco freq.
1/5k
Incomum
1/2k
Prevalência
0.0
Europe
Início
Infancy
🏥
SUS: Cobertura mínimaScore: 35%
Centros em: RS, PR, SC, PA, PE +10CID-10: Q25.7
🇧🇷Dados SUS / DATASUS
PROCEDIMENTOS SIGTAP (5)
0202010503
Cariótipo — bandas G, Q ou Rgenetic_test
0202010600
Pesquisa de microdeleções/microduplicações por FISHlab_test
0202010694
Sequenciamento completo do exoma (WES)rehabilitation
0202010260
Dosagem de alfa-fetoproteína
0301070040
Atendimento em reabilitação — doenças raras
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Entender a doença

Do básico ao detalhe, leia no seu ritmo

Preparando trilha educativa...

Sinais e sintomas

O que aparece no corpo e com que frequência cada sintoma acontece

Partes do corpo afetadas

🫁
Pulmão
5 sintomas
❤️
Coração
3 sintomas
🩸
Sangue
3 sintomas
🧠
Neurológico
2 sintomas
🫃
Digestivo
2 sintomas
🦴
Ossos e articulações
2 sintomas

+ 13 sintomas em outras categorias

Características mais comuns

90%prev.
Fístulas arteriovenosas pulmonares
Muito frequente (99-80%)
90%prev.
Telangiectasia
Muito frequente (99-80%)
55%prev.
Hemotórax
Frequente (79-30%)
55%prev.
Acidente vascular cerebral isquêmico
Frequente (79-30%)
55%prev.
Hipoxemia
Frequente (79-30%)
55%prev.
Ataque isquêmico transitório
Frequente (79-30%)
30sintomas
Muito frequente (2)
Frequente (6)
Ocasional (16)
Muito raro (4)
Sem dados (2)

Os sintomas variam de pessoa para pessoa. Abaixo estão as 30 características clínicas mais associadas, ordenadas por frequência.

Fístulas arteriovenosas pulmonaresPulmonary arteriovenous fistulas
Muito frequente (99-80%)90%
Telangiectasia
Muito frequente (99-80%)90%
HemotóraxHemothorax
Frequente (79-30%)55%
Acidente vascular cerebral isquêmicoIschemic stroke
Frequente (79-30%)55%
HipoxemiaHypoxemia
Frequente (79-30%)55%

Linha do tempo da pesquisa

Publicações por ano — veja quando o interesse científico cresceu
Anos de pesquisa1desde 2026
Total histórico840PubMed
Últimos 10 anos200publicações
Pico202555 papers
Linha do tempo
2026Hoje · 2026🧪 1996Primeiro ensaio clínico📈 2025Ano de pico
Publicações por ano (últimos 10 anos)

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Genética e causas

O que está alterado no DNA e como passa nas famílias

🧬

Nenhum gene associado encontrado

Os dados genéticos desta condição ainda estão sendo catalogados.

Diagnóstico

Os sinais que médicos procuram e os exames que confirmam

Carregando...

Tratamento e manejo

Remédios, cuidados de apoio e o que precisa acompanhar

Pipeline de tratamentos
Pipeline regulatório — de medicamentos já aprovados a drogas em pesquisa exploratória.
·Pré-clínico8
Medicamentos catalogadosEnsaios clínicos· 0 medicamentos · 8 ensaios
Carregando informações de tratamento...

Onde tratar no SUS

Hospitais de referência no Brasil e o protocolo oficial do SUS (PCDT)

🇧🇷 Atendimento SUS — Malformação arteriovenosa pulmonar

Centros de Referência SUS

24 centros habilitados pelo SUS para Malformação arteriovenosa pulmonar

Centros para Malformação arteriovenosa pulmonar

Detalhes dos centros

Hospital Universitário Prof. Edgard Santos (HUPES)

R. Dr. Augusto Viana, s/n - Canela, Salvador - BA, 40110-060 · CNES 0003808

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo

Hospital Infantil Albert Sabin

R. Tertuliano Sales, 544 - Vila União, Fortaleza - CE, 60410-794 · CNES 2407876

Serviço de Referência

Rota
Anomalias CongênitasDeficiência Intelectual

Hospital de Apoio de Brasília (HAB)

AENW 3 Lote A Setor Noroeste - Plano Piloto, Brasília - DF, 70684-831 · CNES 0010456

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Estadual Infantil e Maternidade Alzir Bernardino Alves (HIABA)

Av. Min. Salgado Filho, 918 - Soteco, Vila Velha - ES, 29106-010 · CNES 6631207

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital das Clínicas da UFG

Rua 235 QD. 68 Lote Área, Nº 285, s/nº - Setor Leste Universitário, Goiânia - GO, 74605-050 · CNES 2338424

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo

Hospital Universitário da UFJF

R. Catulo Breviglieri, Bairro - s/n - Santa Catarina, Juiz de Fora - MG, 36036-110 · CNES 2297442

Atenção Especializada

Rota
Anomalias Congênitas

Hospital das Clínicas da UFMG

Av. Prof. Alfredo Balena, 110 - Santa Efigênia, Belo Horizonte - MG, 30130-100 · CNES 2280167

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Universitário Julio Müller (HUJM)

R. Luis Philippe Pereira Leite, s/n - Alvorada, Cuiabá - MT, 78048-902 · CNES 2726092

Atenção Especializada

Rota
Anomalias Congênitas

Hospital Universitário João de Barros Barreto

R. dos Mundurucus, 4487 - Guamá, Belém - PA, 66073-000 · CNES 2337878

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Universitário Lauro Wanderley (HULW)

R. Tabeliao Estanislau Eloy, 585 - Castelo Branco, João Pessoa - PB, 58050-585 · CNES 0002470

Atenção Especializada

Rota
Anomalias Congênitas

Instituto de Medicina Integral Prof. Fernando Figueira (IMIP)

R. dos Coelhos, 300 - Boa Vista, Recife - PE, 50070-902 · CNES 0000647

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Pequeno Príncipe

R. Des. Motta, 1070 - Água Verde, Curitiba - PR, 80250-060 · CNES 3143805

Serviço de Referência

Rota
Anomalias CongênitasDeficiência Intelectual

Hospital Universitário Regional de Maringá (HUM)

Av. Mandacaru, 1590 - Parque das Laranjeiras, Maringá - PR, 87083-240 · CNES 2216108

Atenção Especializada

Rota
Anomalias Congênitas

Hospital de Clínicas da UFPR

R. Gen. Carneiro, 181 - Alto da Glória, Curitiba - PR, 80060-900 · CNES 2364980

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Universitário Pedro Ernesto (HUPE-UERJ)

Blvd. 28 de Setembro, 77 - Vila Isabel, Rio de Janeiro - RJ, 20551-030 · CNES 2280221

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo

Instituto Nacional de Saúde da Mulher, da Criança e do Adolescente Fernandes Figueira (IFF/Fiocruz)

Av. Rui Barbosa, 716 - Flamengo, Rio de Janeiro - RJ, 22250-020 · CNES 2269988

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital São Lucas da PUCRS

Av. Ipiranga, 6690 - Jardim Botânico, Porto Alegre - RS, 90610-000 · CNES 2232928

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo

Hospital de Clínicas de Porto Alegre (HCPA)

Rua Ramiro Barcelos, 2350 Bloco A - Av. Protásio Alves, 211 - Bloco B e C - Santa Cecília, Porto Alegre - RS, 90035-903 · CNES 2237601

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital Universitário da UFSC (HU-UFSC)

R. Profa. Maria Flora Pausewang - Trindade, Florianópolis - SC, 88036-800 · CNES 2560356

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo

Hospital das Clínicas da FMUSP

R. Dr. Ovídio Pires de Campos, 225 - Cerqueira César, São Paulo - SP, 05403-010 · CNES 2077485

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital de Base de São José do Rio Preto

Av. Brg. Faria Lima, 5544 - Vila Sao Jose, São José do Rio Preto - SP, 15090-000 · CNES 2079798

Atenção Especializada

Rota
Anomalias Congênitas

Hospital de Clínicas da UNICAMP

R. Vital Brasil, 251 - Cidade Universitária, Campinas - SP, 13083-888 · CNES 2748223

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

Hospital de Clínicas de Ribeirão Preto (HCRP-USP)

R. Ten. Catão Roxo, 3900 - Vila Monte Alegre, Ribeirão Preto - SP, 14015-010 · CNES 2082187

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do MetabolismoDeficiência Intelectual

UNIFESP / Hospital São Paulo

R. Napoleão de Barros, 715 - Vila Clementino, São Paulo - SP, 04024-002 · CNES 2688689

Serviço de Referência

Rota
Anomalias CongênitasErros Inatos do Metabolismo
Sobre os centros SUS: Estes centros são habilitados pelo Ministério da Saúde como Serviços de Referência em Doenças Raras ou Serviços de Atenção Especializada. O atendimento é pelo SUS, com encaminhamento da rede de atenção básica.

Dados de DATASUS/CNES, SBGM, ABNeuro e Ministério da Saúde. Sempre confirme a disponibilidade diretamente com o estabelecimento.

Pesquisa ativa

Ensaios clínicos abertos e novidades científicas recentes

🟢 Recrutando agora

4 pesquisas recrutando participantes. Converse com seu médico sobre a possibilidade de participar.

Outros ensaios clínicos

11 ensaios clínicos encontrados, 4 ativos.

Distribuição por fase
Ver todos no ClinicalTrials.gov
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Publicações mais relevantes

🥇Melhor nível de evidência: Revisão sistemática
Timeline de publicações
470 papers (10 anos)
#1

Safety and Efficacy of the LOBO Vascular Occlusion Device for Embolization of Pulmonary Arteriovenous Malformations (PAVM): A Single-Center Retrospective Experience.

Journal of vascular and interventional radiology : JVIR2026 Mar 16

To evaluate the safety, technical success, and short-term clinical efficacy of the Low-profile Braided Occluder (LOBO) device for embolization of pulmonary arteriovenous malformations (PAVMs). A single-center retrospective study of 23 consecutive patients (mean 42.3 + 19 years; 82% female) with PAVMs underwent transcatheter embolization using LOBO devices. Clinical efficacy was defined as the absence of PAVM recanalization/persistence and ≥70% reduction in sac size on 6-month follow-up CT angiography (CTA). Adverse events were also assessed following embolization. Of the twenty-three patients treated, 87% had Hereditary Hemorrhagic Telangiectasia. Fifty-nine feeding arteries were embolized using a single device per feeder (LOBO-3, n=37; LOBO-5, n=18; LOBO-7, n=3; LOBO-9, n=1) with no additional coils or other embolic devices required. Mean feeding-artery diameter was 2.93+1.05 mm. The mean fluoroscopy time was 29.19 + 20 minutes (Median:24.9 minutes; Range: 4.6-106.9 minutes), and mean radiation dose was 623.5 + 598 mGy (Median:404 mGy; Range: 18-3135 mGy). Technical success was 100%, with no intraprocedural device mal-deployment or migration. At imaging follow-up of approximately 6 months (Mean 251+74.55 days, Median 266 days, Range 154 - 474 days), there was no recanalization of treated arterial feeders and nopersistence or recanalization of the PAVM sac. No device-related adverse events or major procedure-related adverse events were observed. In this single-center experience, the LOBO device appears to be a safe and effective option for PAVM embolization, with promising short-term results.

#2

BMPR2 Splice-Site Variant in a Patient With Pulmonary Arteriovenous Malformation and Delayed-Onset Pulmonary Arterial Hypertension: A Case Report and Mechanistic Phenocopy Hypothesis.

American journal of medical genetics. Part A2026 Mar 08

Pulmonary arteriovenous malformations (PAVMs) are rare vascular anomalies most commonly seen in hereditary hemorrhagic telangiectasia (HHT), a condition associated with mutations in ENG, ACVRL1, SMAD4, or GDF2. In contrast, BMPR2 variants are well-established in heritable pulmonary arterial hypertension (PAH), but their relationship to PAVMs remains poorly understood. We report the case of a 41-year-old woman with an incidentally discovered PAVM, initially treated with embolization and subsequent surgical resection. She remained asymptomatic for several years until progressive exertional dyspnea led to a diagnosis of severe precapillary PAH. Genetic testing identified a heterozygous BMPR2 splice-site variant (c.967 + 5G>A), previously reported in a PAH cohort but currently classified as a variant of uncertain significance. This report is notable for the delayed evolution from isolated PAVM to PAH in the context of a BMPR2 variant, raising the possibility of a mechanistic link outside the canonical HHT pathway. We review published reports of BMPR2-associated PAVMs, some of which include subtle HHT-like features, such as mucocutaneous telangiectases and epistaxis, despite negative testing for classical HHT genes. These observations suggest a potential phenocopy vascular syndrome driven by disruption of the shared bone morphogenetic protein 9 (BMP9)-ALK1 signaling axis. We also discuss the implications of sotatercept, a transforming growth factor-beta (TGF-β) superfamily ligand trap, which in this case was associated with symptomatic improvement and stable shunt burden. These findings contribute to the emerging recognition of atypical vascular phenotypes in BMPR2 variant carriers, particularly those presenting with PAVMs in the absence of HHT. It highlights the importance of considering genetic testing in isolated AVM presentations, as well as the need for longitudinal surveillance and mechanistic investigation into overlapping TGF-β/BMP signaling disorders.

#3

Four-Dimensional Computed Tomography Differentiates Congenital Right Pulmonary Vein Atresia From Suspected Arteriovenous Malformation: A Case Report.

Respirology case reports2026 Mar

Congenital pulmonary vein atresia (PVA) is a rare condition often associated with vascular anomalies and complex pulmonary hemodynamics. A 54-year-old woman was referred for evaluation of a nodular shadow in the right upper lobe, initially suspected to represent a pulmonary arteriovenous malformation (PAVM). Four-dimensional enhanced computed tomography (4D-CT) revealed no abnormal vessels, suggesting a PAVM in the pulmonary arterial phase. However, in the venous phase, the pulmonary vein of the right upper lobe was occluded at the trunk, with reflux via a pulmonary vein varix and an abnormal vein draining into the pulmonary vein of the right middle lobe. Due to the risk of pulmonary hypertension, thromboembolism, or varix rupture, the patient underwent right upper lobectomy. 4D-CT effectively delineates the vascular morphology by separating the pulmonary arterial and venous phases. Congenital PVA may involve pulmonary vein varices and abnormal vascular formation; 4D-CT may be valuable for diagnosis and treatment planning.

#4

Pulmonary arteriovenous malformation in pregnancy: a case report and literature review.

Maternal health, neonatology and perinatology2026 Mar 03

Pulmonary arteriovenous malformations (PAVMs) are rare vascular anomalies often linked to hereditary hemorrhagic telangiectasia (HHT). Pregnancy-related hemodynamic and hormonal changes may exacerbate PAVMs and lead to serious maternal and fetal complications. A 26-year-old multipara at 25 weeks’ gestation presented with fever, cough, progressive dyspnea and left chest pain. Imaging demonstrated bilateral PAVMs with a loculated left pleural effusion. She was managed conservatively (intercostal drainage, transfusion, thromboprophylaxis) and monitored closely. Embolization was discussed but deferred after multidisciplinary discussion because of insufficient finances and the patient’s clinical stability; elective cesarean section at 39 weeks resulted in a healthy newborn. The patient was referred to interventional radiology for planned postpartum embolization. To report an unusual presentation of bilateral large PAVMs in pregnancy and to review the literature on diagnostic strategies, antenatal management (embolotherapy vs. surgery vs. conservative), and maternal–fetal outcomes. We searched PubMed/MEDLINE, Embase and Scopus (Jan 1, 1997–Sep 30, 2025) using combinations of MeSH/keywords: “pulmonary arteriovenous malformation”, “PAVM”, “pulmonary AVM”, “pregnancy”, “pregnant”, “embolization”, “embolotherapy”, “hemothorax” (English, human). Case reports, case series and observational studies reporting PAVM in pregnancy were included; reviews and animal studies were excluded. Bibliographies of included articles were hand searched. A total of 21 published cases of PAVM in pregnancy were identified; after excluding the cases summarized in the earlier review up to 1997, we focused on 12 subsequent reports (Table 1). Dyspnea and chest pain were the most frequent presentations. Antenatal embolization was performed in several cases with generally favorable outcomes, though recanalization/persistence has been reported. No maternal deaths were reported among the cases included in our review. PAVM in pregnancy can present emergently and requires individualized, multidisciplinary management. Transcatheter embolization is the preferred treatment when feasible, but case-by-case decisions — accounting for clinical stability, gestation, and patient factors — are essential.

#5

An Uncommon Cause of Massive Hemothorax: Pulmonary Arteriovenous Malformation in the Right Middle Lobe.

Open respiratory archives2026

Pulmonary arteriovenous malformations (PAVMs) are rare vascular anomalies that can lead to severe complications when ruptured. We report the case of a 65-year-old active smoker who presented to the emergency department with acute pleuritic chest pain, severe dyspnea, and hypoxemia. Chest CT revealed a large PAVM in the right middle lobe, associated with massive hemothorax and a small pneumothorax. The patient had no history of hereditary hemorrhagic telangiectasia. Initial management included pleural drainage and endovascular embolization with a 16 mm Amplatzer™ device. Due to persistent respiratory failure and high risk of rebleeding, a right middle lobectomy was subsequently performed. Intraoperative findings confirmed a partially thrombosed AVM and correct device placement. Postoperative recovery was uneventful, with no recurrent bleeding. This case highlights a rare cause of spontaneous massive hemothorax requiring combined endovascular and surgical management, emphasizing the importance of early diagnosis and multidisciplinary care in idiopathic PAVMs. Las malformaciones arteriovenosas pulmonares (MAVPs) son anomalías vasculares poco frecuentes que pueden originar complicaciones graves cuando se rompen. Se trata de un paciente varón de 65 años y fumador activo que acudió al servicio de Urgencias con disnea intensa, dolor torácico de características pleuríticas e hipoxemia. La TC de tórax mostró una gran MAVP en el lóbulo medio derecho, asociada a hemotórax masivo y un pequeño neumotórax. El paciente no tenía antecedentes de telangiectasia hemorrágica hereditaria (THH). Se colocó un drenaje pleural y se realizó una embolización endovascular con dispositivo Amplatzer™ de 16 mm. Además, debido a la persistencia de insuficiencia respiratoria y riesgo elevado de resangrado, se realizó una lobectomía media derecha. Durante la intervención se confirmó una MAV parcialmente trombosada y la adecuada ubicación del dispositivo. La evolución posoperatoria fue favorable, sin nuevos sangrados. Este caso destaca una causa infrecuente de hemotórax espontáneo masivo que puede requerir tratamiento combinado endovascular y quirúrgico, resaltando la importancia de una sospecha clínica precoz y el manejo multidisciplinar en las MAVPs idiopáticas.

Publicações recentes

Ver todas no PubMed

📚 EuropePMC524 artigos no totalmostrando 196

2026

Safety and Efficacy of the LOBO Vascular Occlusion Device for Embolization of Pulmonary Arteriovenous Malformations (PAVM): A Single-Center Retrospective Experience.

Journal of vascular and interventional radiology : JVIR
2026

BMPR2 Splice-Site Variant in a Patient With Pulmonary Arteriovenous Malformation and Delayed-Onset Pulmonary Arterial Hypertension: A Case Report and Mechanistic Phenocopy Hypothesis.

American journal of medical genetics. Part A
2026

Four-Dimensional Computed Tomography Differentiates Congenital Right Pulmonary Vein Atresia From Suspected Arteriovenous Malformation: A Case Report.

Respirology case reports
2026

Pulmonary arteriovenous malformation in pregnancy: a case report and literature review.

Maternal health, neonatology and perinatology
2026

Incidental pulmonary arteriovenous malformation.

Journal of hospital medicine
2026

Incidental diagnosis of a lingular pulmonary arteriovenous malformation in a 22-year-old female: a rare case report from Syria.

BMC pulmonary medicine
2026

An Uncommon Cause of Massive Hemothorax: Pulmonary Arteriovenous Malformation in the Right Middle Lobe.

Open respiratory archives
2026

The dual masquerade of the headache culprit: unravelling the collaborative crime of patent foramen ovale and multiple pulmonary arteriovenous malformations.

Acta cardiologica
2026

Prospective evaluation of time-resolved MRA in diagnosing and monitoring pulmonary arteriovenous malformations.

Acta radiologica (Stockholm, Sweden : 1987)
2026

Long-term Echocardiographic Features After Percutaneous Closure of Patent Foramen Ovale.

Interventional cardiology (London, England)
2026

Massive Resting Shunt on c-TCD: A Clue to Pulmonary Arteriovenous Malformation in a Young Stroke Patient.

Balkan medical journal
2026

Hereditary hemorrhagic telangiectasia patient with pulmonary arteriovenous malformation: A case report.

Medicine
2026

Vascular whispers and anaemia: Unravelling hereditary haemorrhagic telangiectasia.

Medical journal, Armed Forces India
2025

Recurrent Stroke Due to Pulmonary Arteriovenous Malformation: Diagnostic Challenges and Management.

Cureus
2025

How Early Veno-Venous Malformation Can Jeopardize a Perfect Kawashima Repair: A Compilation of Two Cases and Review of Literature.

Cureus
2025

From Headache to Hydrocephalus: The Hidden Pulmonary Arteriovenous Malformation Behind Multiple Brain Abscesses.

Annals of African medicine
2025

Decreased endothelial cell retinoic acid signaling accelerates progression of single ventricle pulmonary arteriovenous malformations.

bioRxiv : the preprint server for biology
2025

Emerging Techniques and Treatment Outcomes in Pulmonary Arteriovenous Malformations Embolisation: A Narrative Review.

Journal of clinical medicine
2025

Ruptured pulmonary AV malformation presenting as spontaneous haemothorax in pregnancy.

BMJ case reports
2025

Pulmonary arteriovenous malformation: the missing link?

Thorax
2026

Patient-Friendly Summary of the ACR Appropriateness Criteria®: Pulmonary Arteriovenous Malformation (PAVM).

Journal of the American College of Radiology : JACR
2025

A case of hereditary hemorrhagic telangiectasia with hypoxemia onset in the neonatal period.

BMC pulmonary medicine
2025

Case Report: Pregnancy complicated with pulmonary arteriovenous malformation-diagnosis and surgical management.

Frontiers in surgery
2025

Amplatzer vascular plug use for the treatment of pulmonary arteriovenous malformation.

Lung India : official organ of Indian Chest Society
2025

From Scar to Shunt: Incidental Discovery of Pulmonary Arteriovenous Malformation in a Healthy Adult Trauma Patient.

Cureus
2025

Vascular and Non-Vascular Intervention in the Pediatric Chest: An Update.

Cardiovascular and interventional radiology
2025

Hemodynamic outcomes in patients undergoing bidirectional cavopulmonary connection with additional or antegrade pulmonary blood flow: a single-centre retrospective study.

PeerJ
2025

Clinical practice variability among paediatric interventional cardiologists assessing pulmonary arteriovenous malformations.

Cardiology in the young
2025

Risk of Recurrent Stroke Among Patients With Patent Foramen Ovale vs Pulmonary Arteriovenous Malformation: A Nationwide Study.

Neurology
2025

Unanticipated Hypoxemia in Late Pregnancy Revealing Hereditary Hemorrhagic Telangiectasia.

Internal medicine (Tokyo, Japan)
2026

Pulmonary Arteriovenous Malformation Embolization: The Role of Contrast-Enhanced CT and Standardized Outcome Measures.

Journal of vascular and interventional radiology : JVIR
2025

Turner syndrome with pulmonary arteriovenous malformation: a case report.

Frontiers in cardiovascular medicine
2026

Successfully Treating Pulmonary Arteriovenous Malformation and Pulmonary Arterial Hypertension in a Patient with GDF2 Variant.

Archivos de bronconeumologia
2026

Successful Antenatal Embolization of a Complex Pulmonary Arteriovenous Malformation in the Third Trimester of Pregnancy: A Case Report.

Vascular and endovascular surgery
2025

Chronic cyanosis since infancy: Unveiling a giant right pulmonary arteriovenous malformation.

Radiology case reports
2025

Bumping Into Doors: A Case Report of Brain Abscess as a Complication of Pulmonary Arteriovenous Malformation.

Cureus
2025

Cerebral and Portal Venous Air Embolism: A Complication of PICC Line Placement.

Case reports in radiology
2025

Corrigendum to "Pulmonary arteriovenous malformation: Challenging diagnosis: A case report" [Radiol Case Rep 18, (2023) 3777-3780].

Radiology case reports
2025

Pulmonary Arterious Malformation as Rare Cause of ST-Segment Elevation Myocardial Infarction.

JACC. Case reports
2025

A large pulmonary arteriovenous malformation in an adolescent girl - timely diagnosis and treatment: a case report.

Paediatrics and international child health
2025

Pediatric Pulmonary Arteriovenous Malformations in Patients with Hereditary Hemorrhagic Telangiectasia: Screening, Diagnosis, and Management.

Journal of clinical medicine
2025

Congenital Pulmonary Airway Malformation with Pulmonary Arteriovenous Malformation in Adulthood: A Case Report.

Surgical case reports
2025

A 63-year-old woman with hypoxemic respiratory failure due to pulmonary arteriovenous malformation.

Polish archives of internal medicine
2025

Feeding-Artery Microvascular Plug Embolization Versus Nidus-Plus-Feeding-Artery Coil Embolization of Pulmonary Arteriovenous Malformations.

Journal of clinical medicine
2025

A novel SMAD9 nonsense variant in an 11-year-old Japanese patient with diffuse pulmonary arteriovenous malformation: A case report.

Journal of cardiology cases
2025

Pulmonary arteriovenous malformation diagnosed by recurrent hemothorax - A case report.

Respiratory medicine case reports
2025

ACVRL1 and MTHFR double variants in an adolescent with paradoxical cerebral embolism.

Pediatrics international : official journal of the Japan Pediatric Society
2025

Successful coil embolization of 3 pulmonary arteriovenous malformations using a gadolinium contrast agent in a patient with severe iodine allergy: A case report.

Radiology case reports
2025

Differentiating systemic artery-to-pulmonary artery fistula from pulmonary arteriovenous malformation: A case report.

Radiology case reports
2025

Transarterial Embolization for Pulmonary Arteriovenous Malformation: A Systematic Review and Meta-Analysis.

Journal of vascular and interventional radiology : JVIR
2025

Surgical resection of diffuse pulmonary arteriovenous malformations (PAVMs).

JTCVS open
2025

3D Printing in the Management of Pulmonary Arteriovenous Malformation.

JACC. Case reports
2025

Transcatheter closure of a huge complex pulmonary arteriovenous malformation with four devices: a case report.

Cardiology in the young
2025

Pulmonary arteriovenous malformation causing lung sequestration and media infarction: a case report.

Frontiers in medicine
2025

Recurrent "transient ischemic attacks" caused by pulmonary arteriovenous malformation.

Respiratory medicine case reports
2025

Transoesophageal echocardiography in diagnosing pulmonary arteriovenous malformation.

BMJ case reports
2025

Life-threatening massive hemoptysis due to pulmonary arteriovenous malformation: An uncommon case.

Radiology case reports
2025

Management of coexisting patent foramen ovale and pulmonary arteriovenous malformation: a case report of sequential closure.

European heart journal. Case reports
2025

MiR-25-3p regulates pulmonary arteriovenous malformation after Glenn procedure in patients with univentricular heart via the PHLPP2-HIF-1α axis.

Scientific reports
2025

Embolotherapy for Pulmonary Arteriovenous Malformations in the Pediatric Population with Hereditary Hemorrhagic Telangiectasias-A Retrospective Case Series.

Journal of vascular and interventional radiology : JVIR
2024

Idiopathic pulmonary arteriovenous malformation: a rarity in clinical practice.

Jornal vascular brasileiro
2025

A case of simultaneous bilateral pulmonary resection for arteriovenous pulmonary malformation.

Indian journal of thoracic and cardiovascular surgery
2025

Conservative Pulmonary Arteriovenous Malformation Screening in Children: Re-Evaluation of Safety.

Pediatric pulmonology
2024

Short-term efficacy of right-to-left shunt closure in patients with vestibular migraine.

Frontiers in neurology
2025

The "pseudo-pulmonary AVM sign": an aid to the diagnosis of histoplasmosis and differentiation from pulmonary arteriovenous malformations.

Current problems in diagnostic radiology
2025

Female patient with telangiectasia, epistaxis and pulmonary arteriovenous malformation.

European journal of internal medicine
2024

Pulmonary Arteriovenous Malformation: Not all Hypoxemia During Covid-19 is the Same.

European journal of case reports in internal medicine
2025

Uncorrectable hypoxemia due to large pulmonary arteriovenous malformation in a patient with myocardial infarction: a case report.

Journal of Yeungnam medical science
2025

Imaging and endovascular management of haemoptysis in congenital heart disease.

The British journal of radiology
2025

A Meta-Analysis and Meta-Regression of Embolisation Outcomes of Pulmonary Arteriovenous Malformations.

Cardiovascular and interventional radiology
2025

Percutaneous closure of pulmonary arteriovenous malformation and concomitant patent foramen ovale for cryptogenic stroke.

The Journal of invasive cardiology
2025

Pulmonary arteriovenous malformation in children.

Pediatric pulmonology
2024

Endovascular embolization of a congenital inferior phrenic artery-to-pulmonary arteriovenous malformation: a rare case report.

BMC pulmonary medicine
2025

Graded Transthoracic Contrast Echocardiography After Pulmonary Arteriovenous Malformation Embolization: Can Chest CT Scan Be Avoided in Patients With a Low-Grade Shunt?

Chest
2024

Hereditary haemorrhagic telangiectasias with recurrent ischemic stroke hinted by manganese deposition in the basal ganglia: a case report and literature review.

BMC neurology
2024

Multimodal ultrasound imaging for patent foramen ovale and pulmonary arteriovenous malformation in patients with cryptogenic stroke or migraine: A prospective diagnostic study.

Medicine
2024

Robotic right lower lobectomy for a persistent large pulmonary arteriovenous malformation following repeated coil embolization.

Journal of vascular surgery cases and innovative techniques
2025

Pulmonary Aneurysmal Arteriovenous Malformation Treated With a Vascular Plug.

Vascular and endovascular surgery
2024

Technical Considerations for Safety and Efficacy: Microballoon-Occluded Transcatheter Embolization Using n-butyl-2-Cyanoacrylate for Treatment of Pulmonary Arteriovenous Malformation.

Cardiovascular and interventional radiology
2024

Catheter embolization for pulmonary arteriovenous malformations during chemotherapy for appendiceal adenocarcinoma: A case report of associated brain abscess.

Radiology case reports
2024

Pulmonary Arteriovenous Malformation in an Unrepaired Tetralogy of Fallot: Diagnostic Implications.

Journal of the Society for Cardiovascular Angiography &amp; Interventions
2024

Pulmonary hypertension exacerbated by hereditary hemorrhagic telangiectasia combined with pulmonary arteriovenous fistula and pregnancy status: A case report.

International journal of cardiology. Cardiovascular risk and prevention
2024

Increased Risk for Infections and Allergic Disease in Hereditary Hemorrhagic Telangiectasia.

Journal of clinical medicine
2024

Percutaneous embolization of pulmonary arteriovenous malformation for the treatment of chronic hypoxemia in a patient with Osler-Weber-Rendu syndrome.

Polish archives of internal medicine
2024

Diffuse pulmonary arteriovenous malformation presenting with secondary polycythemia and headaches: a case report.

Journal of medical case reports
2024

Vascular Plugs Improve Pulmonary Arteriovenous Malformation Occlusion over Coil Embolization Alone: A Proof-of-Concept Study Using Dual-Energy CT.

Journal of vascular and interventional radiology : JVIR
2024

The trade-off dilemma between radiation dose and image resolution.

Diagnostic and interventional imaging
2024

Ruptured pulmonary arteriovenous fistula causing hemothorax in a patient with hereditary hemorrhagic telangiectasia: A case report.

Pulmonary circulation
2024

Massive hemothorax induced by pulmonary arteriovenous malformation rupture: a case report and literature review.

Journal of cardiothoracic surgery
2024

Selective Angiographic Evaluation in Patients with Simple-Type Pulmonary Arteriovenous Malformations Treated with Vascular Plug.

Cardiovascular and interventional radiology
2024

Liver disease and transplantation in telomere biology disorders: An international multicenter cohort.

Hepatology communications
2024

Unveiling the complexity: coexistence of rheumatic heart disease and pulmonary arteriovenous malformation-a unique case report.

European heart journal. Case reports
2024

ACR Appropriateness Criteria® Pulmonary Arteriovenous Malformation (PAVM): 2023 Update.

Journal of the American College of Radiology : JACR
2024

Use Extreme Caution: A Commentary on an Alternative Endovascular Technique for Treatment of Pulmonary Arteriovenous Malformation-Microballoon-Occluded Transcatheter Embolization using n-butyl-2-cyanoacrylate.

Cardiovascular and interventional radiology
2024

Spontaneous haemothorax caused by a ruptured pulmonary arterio-venous malformation: A manifestation of hereditary haemorrhagic telangiectasia in pregnancy.

Obstetric medicine
2024

Large pulmonary arteriovenous malformation lost to follow-up with 10 years of asymptomatic interval growth: A case report.

Radiology case reports
2024

A mediastinum-tumour-like pulmonary arteriovenous malformation with association to the pulmonary artery treated with surgical resection.

Respirology case reports
2024

Case of Prenatal Diagnosis of a Fetal Pulmonary Arteriovenous Malformation at Term.

Diagnostics (Basel, Switzerland)
2024

Angiographic tool to detect pulmonary arteriovenous malformations in single ventricle physiology.

Cardiology in the young
2024

Recurrence of Pulmonary Arteriovenous Malformation after Embolization in Patients with Pulmonary Hypertension.

Journal of vascular and interventional radiology : JVIR
2024

[Ischemic stroke due to paradoxical embolism through pulmonary arteriovenous malformation in a young patient].

Medicina
2024

Ultra-low dose chest CT for the diagnosis of pulmonary arteriovenous malformation in patients with hereditary hemorrhagic telangiectasia.

Diagnostic and interventional imaging
2024

Successful embolization of a clinically significant pulmonary arteriovenous malformation.

Respirology case reports
2024

An Alternative Endovascular Technique for Treatment of Pulmonary Arteriovenous Malformation: Microballoon-occluded Transcatheter Embolization Using n-butyl-2-cyanoacrylate.

Cardiovascular and interventional radiology
2024

Hereditary hemorrhagic telangiectasia diagnosis: A case report.

Journal of pediatric nursing
2024

Life-threatening hemothorax due to rupture of pulmonary arteriovenous malformation during pregnancy.

Journal of surgical case reports
2024

Complex pulmonary arteriovenous malformation in a boy aged 18 months.

Anales de pediatria
2024

Fusion imaging for guidance of pulmonary arteriovenous malformation embolisation with minimal radiation and contrast exposure.

Cardiology in the young
2024

Massive Pulmonary Arteriovenous Malformation as a Cause of Fetal Heart Failure.

Cureus
2024

Evaluation of a gradually enlarging complex pulmonary arteriovenous malformation consisting of innumerable small fistulae using four-dimensional computed tomography.

BMJ case reports
2024

Embolization of De Novo Pulmonary Arteriovenous Malformations Using High-Volume Detachable Non-Fibered Coils: Propensity-Matched Comparison to Traditional Coils.

Journal of clinical medicine
2024

Coil Embolization of a Large Recurrent Pulmonary Arteriovenous Malformation by Retrograde Transseptal Pulmonary Vein Access.

Journal of vascular and interventional radiology : JVIR
2024

Use of Polyurethane-Covered Stents for Exclusion of Pulmonary Arteriovenous Malformations.

Cardiovascular and interventional radiology
2023

Spontaneous Hemothorax by Pulmonary Arteriovenous Malformation during Pregnancy.

The Thoracic and cardiovascular surgeon reports
2024

Pulmonary arteriovenous malformations in patients with previous brain abscess: a cross-sectional population-based study.

European journal of neurology
2023

A Congenital Portosystemic Shunt in a Child With Heterotaxy, Situs Inversus, Polysplenia, and Interrupted Inferior Vena Cava With Azygous Continuation.

ACG case reports journal
2023

Case report: video-assisted thoracoscopic surgery for pulmonary arteriovenous malformation using near-infrared fluorescence with indocyanine green.

Journal of cardiothoracic surgery
2023

Pregnancy and delivery after percutaneous embolization with a combination of microvascular plugs and hydrogel-coated coils for unilateral diffuse pulmonary arteriovenous malformations: a case report.

European heart journal. Case reports
2023

Pulmonary arteriovenous malformation and a concurrent patent ductus arteriosus in a Doberman.

Journal of veterinary cardiology : the official journal of the European Society of Veterinary Cardiology
2023

Cine MRI in the Evaluation of Pulmonary Arteriovenous Malformations.

Cureus
2023

A case of hemoptysis unveiling the unlikely culprit - pulmonary arteriovenous malformation.

Radiology case reports
2023

Pulmonary arteriovenous malformation: Challenging diagnosis: A case report.

Radiology case reports
2023

Incidental radiological findings during clinical tuberculosis screening in Lesotho and South Africa: a case series.

Journal of medical case reports
2023

An Update on Embolization for Pulmonary Arteriovenous Malformations.

Interventional radiology (Higashimatsuyama-shi (Japan)
2023

An analysis of sex differences in pulmonary arteriovenous malformation presentation, complications and management in a large, multinational registry of patients with hereditary haemorrhagic telangiectasia.

ERJ open research
2023

Retrospective single-arm cohort study of video-assisted thoracic surgery for treatment of idiopathic peripherally located simple type pulmonary arteriovenous malformation in 23 consecutive patients.

Journal of cardiothoracic surgery
2023

Pearls and Pitfalls in the Transesophageal Echocardiographic Diagnosis of Patent Foramen Ovale.

Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography
2023

Comparison of Transthoracic Contrast Echocardiography with High-Resolution Chest CT after Embolization of Pulmonary Arteriovenous Malformation.

Journal of vascular and interventional radiology : JVIR
2023

CT chest-cerebral angiography for basilar artery occlusion caused by pulmonary arteriovenous malformation.

BMJ case reports
2023

[Hereditary hemorrhagic telangiectasia].

Revue des maladies respiratoires
2023

Twenty-Seven-Year Retrospective Review of Hemoptysis from Systemic Collaterals Following Pulmonary Arteriovenous Malformation Embolization.

Cardiovascular and interventional radiology
2023

Pulmonary Arteriovenous Malformation Unmasked by Pregnancy: A Review of Pulmonary Arteriovenous Malformations and Cardiovascular and Respiratory Changes in Pregnancy.

Case reports in pulmonology
2023

Pulmonary arteriovenous fistula in a rare location: The importance of excluding patent foramen ovale.

Journal of cardiology cases
2023

Pulmonary Arteriovenous Malformation (With Secondary Erythrocytosis): A Diagnosis Hastened by COVID-19 Pandemic.

Mayo Clinic proceedings
2023

Giant complex pulmonary arteriovenous malformation treated with coil embolisation under general anaesthesia with a history of contrast media allergy.

BMJ case reports
2023

Double anterograde/retrograde approach for embolization of pulmonary arteriovenous malformation presenting with acute respiratory failure.

European heart journal
2023

Abernethy Malformation Masquerading as Congenital Heart Disease: A Boy With Cyanosis, Clubbing, and Hypoxia.

Cureus
2023

Mechanical thrombectomy for acute paradoxical cerebral embolism due to pulmonary arteriovenous malformation: A case report and review of literature.

Surgical neurology international
2022

Pulmonary Arteriovenous Malformation in a Rare Case of Hereditary Hemorrhagic Telangiectasia.

Cureus
2023

Spontaneous hemothorax in pregnant patient with pulmonary arteriovenous malformation.

Radiology case reports
2022

Risk factors for cerebral complications in patients with pulmonary arteriovenous malformations: A multicenter retrospective cohort study.

PloS one
2022

Pyogenic brain abscess associated with an incidental pulmonary arteriovenous malformation.

BMJ case reports
2023

Evolution of Pulmonary Arteriovenous Malformations: The Role of Contrast Echocardiography.

Chest
2023

Acute Ischemic Stroke in Patients With Pulmonary Arteriovenous Malformations: Paradoxical Embolism or Epiphenomenon?

Stroke (Hoboken, N.J.)
2022

Telangiectatic pulmonary arteriovenous malformation presenting as a suspected malignant part-solid nodule.

British journal of hospital medicine (London, England : 2005)
2022

Haemothorax in a Pregnant Woman Secondary to Rupture of a Pulmonary Arteriovenous Malformation.

European journal of case reports in internal medicine
2022

Recurrent pulmonary arteriovenous malformation in a patient with Sjögren syndrome: A case report.

Medicine
2022

Transcatheter closure of congenital portosystemic shunts - A multicenter experience.

Annals of pediatric cardiology
2023

Percutaneous Puncture Embolization for Recurrent Pulmonary Arteriovenous Malformation After Failed Initial Treatment: A Case Report.

Vascular and endovascular surgery
2023

Unexpected Complications 25 Years after Coil Embolization for Pulmonary Arteriovenous Fistula.

Internal medicine (Tokyo, Japan)
2022

Significance of transesophageal contrast echocardiography with the agitated saline test for diagnosing pulmonary arteriovenous malformations.

Frontiers in cardiovascular medicine
2022

Hepatic factor may not originate from hepatocytes.

Frontiers in cardiovascular medicine
2022

Noncontrast time-resolved pulmonary magnetic resonance angiography with consecutive beam saturation pulse and variable flip angles using three-dimensional fast spin echo: A preliminary study.

Magnetic resonance imaging
2023

Diagnosis and Management of Persistent Pulmonary Arterio-venous Malformations following Embolotherapy.

Academic radiology
2022

Advancements in Interventional Oncology of the Chest: Transarterial Chemoembolization and Related Therapies.

Seminars in interventional radiology
2022

Pulmonary Arteriovenous Malformations: What the Interventional Radiologist Should Know.

Seminars in interventional radiology
2023

Transcatheter management of life-threatening pulmonary arteriovenous fistula with extracorporeal membrane oxygenation support in an infant.

Cardiology in the young
2022

A Frameshift RBM10 Variant Associated With TARP Syndrome.

Frontiers in genetics
2023

Postembolization Persistence of Pulmonary Arteriovenous Malformations: A Retrospective Comparison of Coils and Amplatzer and Micro Vascular Plugs Using Propensity Score Weighting.

AJR. American journal of roentgenology
2022

Feasibility of Single-Shot Whole Thoracic Time-Resolved MR Angiography to Evaluate Patients with Multiple Pulmonary Arteriovenous Malformations.

Korean journal of radiology
2022

Bronchoscopy-guided removal of intrabronchial coil migration after coil embolization of pulmonary arteriovenous malformation.

Radiology case reports
2022

Brain abscess associated with Mycoplasma faucium - The initial presentation of pulmonary arteriovenous malformation.

IDCases
2022

Current trends in image-guided chest interventions.

Respirology (Carlton, Vic.)
2023

Neurologic Complications in Hereditary Hemorrhagic Telangiectasia with Pulmonary Arteriovenous Malformations: A Systematic Review.

The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
2022

Endovascular Embolisation of Pulmonary Arteriovenous Malformation Using Amplatzer Vascular Plugs.

Cureus
2022

Pulmonary arteriovenous malformation and inherent complications with solitary lung nodule biopsy-literature overview and case report.

Radiology case reports
2021

Three-dimensional rotational angiography utility in imaging and intervention in a case of pulmonary arteriovenous malformation.

Annals of pediatric cardiology
2022

Management of pulmonary arteriovenous malformations involves additional factors aside from the diameter of feeding arteries: a 3-year case-case retrospective analysis.

Respiratory research
2022

Hemoptysis after coil embolization for pulmonary arteriovenous malformation: Histopathological confirmation of bronchial epithelium extension.

Radiology case reports
2022

Neurovascular Complications and Pulmonary Arteriovenous Malformation Feeding Artery Size.

Annals of the American Thoracic Society
2022

Hypoxia and Polycythemia: A Pediatric Emergency Department Point of Care Ultrasound Diagnosis of Pulmonary Arteriovenous Malformation.

Pediatric emergency care
2022

Pulmonary arteriovenous malformations: A case of missed diagnosis in a neonate.

The Medical journal of Malaysia
2022

Hemodynamic Assessment of a Large Pulmonary Arteriovenous Malformation in a Neonate: Case Report and Review of Literature.

Pediatric cardiology
2022

Intracardiac versus extracardiac shunt in a young man with ischaemic stroke.

BMJ case reports
2022

Venous thrombosis via pulmonary arteriovenous malformation causing acute myocardial infarction in a relatively young female patient.

BMJ case reports
2022

Retrograde Transseptal Pulmonary Vein Transcatheter Plug Closure for Pulmonary Arteriovenous Malformation.

JACC. Case reports
2022

Multimodality imaging of Abernethy malformation.

Echocardiography (Mount Kisco, N.Y.)
2022

Treatment of a rare recurrent pulmonary arteriovenous malformation after multiple embolization by robotic-assisted thoracoscopic surgery.

Journal of surgical case reports
2022

Iatrogenic pulmonary artery perforation associated with 5-Fr catheter manipulation during pulmonary arteriovenous malformation embolization with a vascular plug.

Radiology case reports
2022

Racemose hemangioma revealed by massive intraoperative hemorrhage: A case report.

International journal of surgery case reports
2022

Pulmonary arteriovenous malformation revealing Osler-Weber-Rendu disease: A case report.

Clinical case reports
2022

Acquired pulmonary arteriovenous malformation associated with bronchiectasis: a case report.

Journal of medical case reports
2022

Occult lung metastases of papillary thyroid cancer detected in a resected pulmonary arteriovenous malformation specimen.

Respiratory medicine case reports
2022

Pulmonary Arteriovenous Malformation and Its Vascular Mimickers.

Korean journal of radiology
2022

Assessment of pulmonary arteriovenous malformation with ultra-short echo time magnetic resonance imaging.

European journal of radiology
2022

CT Appearance of Pulmonary Arteriovenous Malformations and Mimics.

Radiographics : a review publication of the Radiological Society of North America, Inc
2022

Concurrent pulmonary arteriovenous malformation and pulmonary embolism causing stroke: a therapeutic dilemma.

CVIR endovascular
2021

Congenital pulmonary varix: Two case reports.

Medicine
2021

Severe Hypoxemia Caused by High-Output Heart Failure and Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia.

JACC. Case reports
2022

Pearls & Oy-sters: Cerebral Abscess Secondary to Pulmonary Arteriovenous Malformation in Hereditary Hemorrhagic Telangiectasia.

Neurology
2021

Pulmonary multifocal arteriovenous malformations lead to ischemic stroke in young adults: a case report and literature review.

Annals of palliative medicine
2021

Pulmonary Arteriovenous Malformations Incidentalloma in a 10-Years-Old Child.

Global pediatric health
2022

A massive pulmonary arteriovenous malformation with platypnoea-orthodeoxia: an important and reversible cause of refractory hypoxaemia.

The Medical journal of Australia
2022

Complex, Isolated Pulmonary Arteriovenous Malformation in Two Children With Severe Cyanosis.

World journal for pediatric &amp; congenital heart surgery
2021

Commentary: sVEGFR1 Is Enriched in Hepatic Vein Blood-Evidence for a Provisional Hepatic Factor Candidate?

Frontiers in pediatrics
2021

[A case of pulmonary arteriovenous malformation treated surgically].

Revue des maladies respiratoires
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Referências e fontes

Bases de dados externas citadas neste artigo

Publicações científicas

Artigos indexados no PubMed ligados a esta doença no grafo RarasNet — título, periódico e PMID direto da fonte, sem intermediação de IA.

  1. Safety and Efficacy of the LOBO Vascular Occlusion Device for Embolization of Pulmonary Arteriovenous Malformations (PAVM): A Single-Center Retrospective Experience.
    Journal of vascular and interventional radiology : JVIR· 2026· PMID 41850521mais citado
  2. BMPR2 Splice-Site Variant in a Patient With Pulmonary Arteriovenous Malformation and Delayed-Onset Pulmonary Arterial Hypertension: A Case Report and&#xa0;Mechanistic Phenocopy Hypothesis.
    American journal of medical genetics. Part A· 2026· PMID 41795626mais citado
  3. Four-Dimensional Computed Tomography Differentiates Congenital Right Pulmonary Vein Atresia From Suspected Arteriovenous Malformation: A Case Report.
    Respirology case reports· 2026· PMID 41777480mais citado
  4. Pulmonary arteriovenous malformation in pregnancy: a case report and literature review.
    Maternal health, neonatology and perinatology· 2026· PMID 41772677mais citado
  5. An Uncommon Cause of Massive Hemothorax: Pulmonary Arteriovenous Malformation in the Right Middle Lobe.
    Open respiratory archives· 2026· PMID 41716743mais citado
  6. The Benefits of an Intracardiac Conduit in the Fontan Operation for Complex Systemic Venous Anomalies in Patients with Single Ventricle Physiology.
    World J Pediatr Congenit Heart Surg· 2026· PMID 41984069recente
  7. Concurrent Patent Foramen Ovale and Pulmonary Arteriovenous Malformation Etiology: Complex Case of Cryptogenic Stroke.
    JACC Case Rep· 2026· PMID 41973884recente
  8. Multifactorial Hypercoagulability Causing Simultaneous STEMI and Pulmonary Embolism in Young Adults With Prothrombin G20210A Mutation.
    JACC Case Rep· 2026· PMID 41954539recente
  9. Role of the Transcranial Doppler Bubble Test in the Diagnostic Pathway of a Patent Foramen Ovale in Embolic Stroke of Undetermined Source.
    Cureus· 2026· PMID 41883901recente

Bases de dados e fontes oficiais

Identificadores e referências canônicas usadas para montar este verbete.

  1. ORPHA:2038(Orphanet)
  2. OMIM OMIM:265140(OMIM)
  3. MONDO:0009930(MONDO)
  4. Busca completa no PubMed(PubMed)
  5. Q52775754(Wikidata)

Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.

Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar

Malformação arteriovenosa pulmonar
Compêndio · Raras BR

Malformação arteriovenosa pulmonar

ORPHA:2038 · MONDO:0009930
Prevalência
Unknown
Herança
Multigenic/multifactorial, Unknown
CID-10
Q25.7 · Outras malformações congênitas da artéria pulmonar
CID-11
Ensaios
4 ativos
Início
Infancy
Prevalência
0.0 (Europe)
MedGen
UMLS
C0155675
EuropePMC
Wikidata
Papers 10a
Evidência
🥇 Rev. sistemática
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