714 results match your criteria Imaging in Arteriovenous Lung Malformation


Hereditary haemorrhagic telangiectasia with atrial septal defect and pulmonary hypertension during advanced pregnancy: a case report and literature review.

J Int Med Res 2022 Mar;50(3):3000605221085427

Department of Gynaecology and Obstetrics, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei Province, China.

Pregnancy complicated with hereditary haemorrhagic telangiectasia (HHT) is a rare condition. This case report presents an extremely rare case with the co-occurrence of HHT and congenital heart disease. In this report, a 43-year-old woman at 36 + 4 weeks of gestation experienced haemoptysis with a volume of approximately 300 ml for the first time. Read More

View Article and Full-Text PDF

A case of an unfortunate tooth fairy visit to a ventilator-dependent child.

Pediatr Pulmonol 2022 06 8;57(6):1555-1556. Epub 2022 Apr 8.

Pediatric Pulmonology Unit, Dana-Dwek Children's Hospital, Tel-Aviv Sourasky Medical Center, Tel Aviv, Israel, affiliated to the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

An 8-year-old boy recently sustained a cerebellar arteriovenous malformation rupture, and subsequently suffered from severe neurological injury and became ventilator-dependent through a tracheostomy. During a routine clinic visit, the parents reported that a loose baby tooth had fallen out and disappeared 7 days earlier. The physical examination was unremarkable, but a chest X-ray demonstrated a foreign body in the left lung and secondary atelectasis. Read More

View Article and Full-Text PDF

Pulmonary arteriovenous malformations may be the only clinical criterion present in genetically confirmed hereditary haemorrhagic telangiectasia.

Thorax 2022 Jun 14;77(6):628-630. Epub 2022 Feb 14.

Genomics England Respiratory Clinical Interpretation Partnership (GeCIP), London, UK

Pulmonary arteriovenous malformations (PAVMs) result in preventable complications demanding specialty care. Underlying hereditary haemorrhagic telangiectasia (HHT) can be identified by genetic testing, if the diagnosis is considered. Retrospectively reviewing 152 unrelated adults with genetically confirmed HHT due to , or , we found that only 104/152 (68%) met a clinical diagnosis of HHT with three Curaçao criteria. Read More

View Article and Full-Text PDF

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

Int J Surg Case Rep 2022 Feb 24;91:106722. Epub 2021 Dec 24.

Department of Thoracic Surgery, Kanazawa Medical University, 1-1 Daigaku Uchinada, Ishikawa 920-0293, Japan. Electronic address:

Introduction And Importance: Bronchial arterial racemose hemangioma is considered to be a type of pulmonary arteriovenous malformation (PAVM). We encountered an extremely rare case of racemose hemangioma, which was identified because of massive bleeding during lung cancer surgery.

Case Presentation: A 71-year-old man was suspected of having lung cancer and underwent a right upper lobectomy. Read More

View Article and Full-Text PDF
February 2022

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

J Med Case Rep 2022 Jan 21;16(1):24. Epub 2022 Jan 21.

Department of Respiratory Medicine, Kanazawa Medical University, 1-1 Daigaku, Uchinada-machi, Kahoku-gun, Ishikawa, 920-0293, Japan.

Background: Pulmonary arteriovenous malformations are mostly caused by congenitally abnormal shunts between pulmonary arteries and pulmonary veins.

Case Presentation: A 74-year-old Japanese woman with a history of bronchiectasis was admitted to our hospital because of dyspnea on exertion. Pulmonary angiography and reconstructed three-dimensional contrast-enhanced computed tomography images showed shunts between pulmonary arteries and pulmonary veins, indicating a diagnosis of pulmonary arteriovenous malformations. Read More

View Article and Full-Text PDF
January 2022

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

Respir Med Case Rep 2022 1;35:101574. Epub 2022 Jan 1.

Department of Thoracic Surgery, Fukuyama City Hospital, Fukuyama, Japan.

A 41-year-old man with exertional dyspnea was referred to our hospital. Chest computed tomography (CT) showed a pulmonary arteriovenous malformation (PAVM) in the left lingular lobe, and magnetic resonance imaging showed a brain abscess. After antimicrobial therapy, the patient underwent thoracoscopic lingulectomy of the PAVM. Read More

View Article and Full-Text PDF
January 2022

Pulmonary Arteriovenous Malformation and Its Vascular Mimickers.

Korean J Radiol 2022 02 4;23(2):202-217. Epub 2022 Jan 4.

Department of Radiology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Pulmonary arteriovenous malformation (AVM) is a congenital vascular disease in which interventional radiologists can play both diagnostic and therapeutic roles in patient management. The diagnosis of pulmonary AVM is simple and can usually be made based on CT images. Endovascular treatment, that is, selective embolization of the pulmonary artery feeding the nidus of the pulmonary AVM, and/or selectively either the nidus or draining vein, has become a first-line treatment with advances in interventional devices. Read More

View Article and Full-Text PDF
February 2022

Congenital pulmonary varix: Two case reports.

Medicine (Baltimore) 2021 Dec;100(51):e28340

Department of Radiology, Kansai Medical University, 2-5-1 Shinmachi, Hirakata, Osaka, Japan.

Rationale: Patients with congenital pulmonary varix are asymptomatic and require no treatment, but the radiological characteristics of a pulmonary varix are similar to those of a pulmonary arteriovenous malformation, which requires treatment. Pulmonary angiography is useful for obtaining information about the dynamics of pulmonary blood flow to differentiate a pulmonary varix from a pulmonary arteriovenous malformation for the purpose of treatment planning. Two cases of congenital pulmonary varices that were differentiated from pulmonary arteriovenous malformations based on pulmonary angiography findings are presented. Read More

View Article and Full-Text PDF
December 2021

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

Neurology 2022 02 8;98(7):292-295. Epub 2021 Dec 8.

From the Department of Clinical Neurosciences (J.I.R., A.K.);Department of Pediatrics (K.W., A.K., M.J.E.), Cumming School of Medicine, University of Calgary; Alberta Children's Hospital Research Institute (A.K., M.J.E.), University of Calgary; Hotchkiss Brain Institute (A.K., M.J.E.), University of Calgary, Alberta, Canada.

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant condition that is linked to a myriad of neurologic complications arising from vascular malformations of the brain, spinal cord, and lungs. Our case describes a previously healthy 3-year-old male who presented to hospital with fever of unknown origin and was found to have a brain abscess stemming from a pulmonary arteriovenous malformation (PAVM). This etiology was identified after a period of diagnostic delay; the medical team was suspicious for a proximal embolic source due to the presence of multiple tiny infarcts seen on MRI of the brain, but transthoracic echocardiogram and head and neck angiogram were unremarkable. Read More

View Article and Full-Text PDF
February 2022

A young female with polycythemia: Pearls in the lung.

Adv Respir Med 2021;89(5):546-547. Epub 2021 Sep 27.

Adesh Institute of Medical Sciences and Research, Bathinda, Punjab, India.

View Article and Full-Text PDF
February 2022

Computed tomography of the airways and lungs in congenital heart disease.

Pediatr Radiol 2021 Sep 25. Epub 2021 Sep 25.

Department of Radiology, Children's Hospital of Philadelphia, 3401 Civic Center Blvd., Philadelphia, PA, 19104, USA.

The presence of airway and lung disease in children with congenital heart disease is commonly observed with both cardiac CT angiography and routine chest CT. In this review we discuss abnormalities encountered on CT imaging of the chest beyond the heart and central vasculature, focusing on the airways, lung parenchyma and peripheral vasculature. Preoperative and postoperative findings are reviewed as well. Read More

View Article and Full-Text PDF
September 2021

Intrapulmonary Arteriovenous Fistula: Unusual Early Complication of Wedge Resection.

Ann Thorac Surg 2022 06 10;113(6):e405-e407. Epub 2021 Sep 10.

Department of Pathology, John Paul II Hospital, Cracow, Poland.

We present a case of an arteriovenous fistula that developed in the early postoperative course after wedge resection of the right upper lobe. A 57-year-old man treated for acute myeloid leukemia was referred from the hematology department because of a right upper-lobe tumor. Wedge resection was performed. Read More

View Article and Full-Text PDF

Massive haemorrhagic complications of ruptured pulmonary arteriovenous malformations: outcomes from a 12 years' retrospective study.

BMC Pulm Med 2021 Jul 13;21(1):230. Epub 2021 Jul 13.

Department of Radiology, Shanghai Pulmonary Hospital, Tongji University School of Medicine, 507 Zhengmin Road, Shanghai, 200433, China.

Background: The life-threatening haemorrhagic complications of pulmonary arteriovenous malformations (PAVMs) are extremely rare, and only described in isolated cases. This study was designed to comprehensively investigate management of ruptured PAVMs.

Methods: We retrospectively assessed clinical and imaging data of ruptured PAVMs to summarize incidence, clinical characteristics, and outcomes following embolisation between January 2008 and January 2021. Read More

View Article and Full-Text PDF

Rare ruptured pulmonary arteriovenous malformation mimicking lung tumor in a girl.

Anatol J Cardiol 2021 07;25(7):E30

Department of Cardiology, Changhai Hospital; Shanghai-China.

View Article and Full-Text PDF

Anesthetic challenges in a child with hereditary hemorrhagic telangiectasia with coexisting pulmonary and cerebral arteriovenous malformations for intracerebral hematoma evacuation: A case report.

J Clin Anesth 2021 11 26;74:110430. Epub 2021 Jun 26.

Department of Anesthesiology, Neuro anaesthesia division, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, Kerala, India.

View Article and Full-Text PDF
November 2021

Young stroke due to pulmonary arteriovenous malformation.

BMJ Case Rep 2021 Jun 21;14(6). Epub 2021 Jun 21.

Neurology, University Hospital Southampton NHS Foundation Trust, Southampton, UK.

Young patients presenting with cryptogenic stroke should be investigated for cardiac and extra-cardiac sources of emboli. We present a patient who was investigated for a cardiac source of emboli, following multiple ischaemic strokes and migraine with aura over a period of 17 years. The events were initially thought to be related to a patent foramen ovale (PFO) on bubble contrast echocardiography, however, due to an unusual flow pattern to the left heart, she underwent a CT angiogram to exclude intrapulmonary shunting. Read More

View Article and Full-Text PDF

[Surgery for Right Pulmonary Arteriovenous Malformation with Recurrent Brain Abscess:Report of a Case].

Kyobu Geka 2021 Jun;74(6):477-480

Department of Thoracic Surgery, Japanese Red Cross Osaka Hospital, Osaka, Japan.

A 68-year-old man was referred to our hospital for further examination for chest abnormal shadow in the right lung field. He had a past history of subarachnoid hemorrhage. He was diagnosed with pulmonary arteriovenous malformation (PAVM) and recommended early treatment, but he didnot accept immediate surgical treatment. Read More

View Article and Full-Text PDF

Acute thrombosis of a giant perimedullary arteriovenous fistula in a pediatric HHT patient.

Interv Neuroradiol 2022 Apr 29;28(2):132-135. Epub 2021 May 29.

Division of Pediatric Pulmonology, Mayo Clinic, Rochester, MN, USA.

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant hereditary disorder that results in arteriovenous malformations (AVMs) in the nose, mucocutaneous surfaces and visceral organs, including lung, brain, liver, bowel and rarely spinal cord. We describe a case of a young child with HHT who presented with acute paraparesis due to acute thrombosis of a spinal perimedullary arteriovenous fistula. Patient underwent coil embolization of spinal arteriovenous shunt with resolution of clinical symptoms. Read More

View Article and Full-Text PDF

Placental Site Trophoblastic Tumor in a Pulmonary Vascular Malformation With Spontaneous Pneumothorax.

Ann Thorac Surg 2022 03 25;113(3):e211-e214. Epub 2021 May 25.

Department of Thoracic Surgery, Mazumdar Shaw Medical Centre, Narayana Health City, Bengaluru, Karnataka, India. Electronic address:

Placental site trophoblastic tumor, a rare variety of gestational trophoblastic disease, is traditionally limited to the uterus, found within the placental implantation site where it can lead to arteriovenous malformations. Gestational trophoblastic diseases are known to metastasize to the lungs, of which choriocarcinomas are the most common. However arteriovenous malformations related to such metastatic lesions are extremely rare. Read More

View Article and Full-Text PDF

Usefulness of dynamic fluorodeoxyglucose positron emission tomography/computed tomography in diagnosing pulmonary arteriovenous malformation mimicking a lung tumour.

Interact Cardiovasc Thorac Surg 2021 10;33(4):665-667

Department of Chest Disease, Faculty of Medicine, Tokat Gaziosmanpasa University, Tokat, Turkey.

A 61-year-old male patient with known kidney dysfunction who underwent a non-contrast thorax CT and was then referred to our department for metabolic assessment of solitary pulmonary nodule (SPN). The patient underwent dynamic FDG PET/CT to differentiate benign from malignant SPN. This case illustrates the usefulness of dynamic FDG PET/CT imaging when assessing SPN especially in patients with suspicion for pulmonary arterio-venous malformation accompanying renal failure or contrast allergy. Read More

View Article and Full-Text PDF
October 2021

Transpleural systemic artery-to-pulmonary artery communications in the absence of chronic inflammatory lung disease. A case series and review of the literature.

Clin Radiol 2021 Sep 23;76(9):711.e9-711.e15. Epub 2021 Apr 23.

Imaging Department, Hammersmith Hospital, Imperial College Healthcare NHS Trust, Du Cane Road, London, W12 0HS, UK.

Aim: To describe the causes and computed tomography (CT) and angiographic appearances of transpleural systemic artery-to-pulmonary artery shunts in patients without chronic inflammatory lung disease and determine their best management.

Materials And Methods: All patients referred to a tertiary referral unit between January 2009 and January 2020 in whom a diagnosis of a systemic-to-pulmonary artery communication without underlying chronic inflammatory lung disease was subsequently made have been included in this report. Medical records and imaging findings were reviewed retrospectively. Read More

View Article and Full-Text PDF
September 2021

Pulmonary arteriovenous malformation with metal allergy.

BMJ Case Rep 2021 Mar 10;14(3). Epub 2021 Mar 10.

Thoracic Surgery, National Hospital Organization Shibukawa Medical Center, Shibukawa, Gunma, Japan.

We present a rare case of single pulmonary arteriovenous malformation (PAVM) with multiple metal allergies, including for platinum. A 47-year-old woman presented to our hospital without any symptoms. Enhanced computed tomography showed a single PAVM in S6 of the right lung. Read More

View Article and Full-Text PDF

[Sudden convulsion with multiple pulmonary nodules in a girl aged 15 years].

Zhongguo Dang Dai Er Ke Za Zhi 2021 Mar;23(3):288-293

Department of Pediatrics, Peking University Third Hospital, Beijing 100191, China.

A girl, aged 15 years, was admitted due to sudden convulsion once and multiple pulmonary nodules on lung CT. Acrocyanosis or acropachy/toe deformity was not observed. Laboratory examinations showed an increase in hemoglobin (162 g/L) and a reduction in arterial partial pressure of oxygen (61. Read More

View Article and Full-Text PDF

Giant Ascending Aortic Aneurysm and Pulmonary Arteriovenous Malformation in the Left Upper Lung Lobe.

Ann Thorac Surg 2021 06 5;111(6):e459. Epub 2021 Mar 5.

Department of Cardiovascular Surgery, Mimihara General Hospital, Osaka, Japan.

View Article and Full-Text PDF

The Lugones Procedure for Surgical Repair of Scimitar Syndrome: Preserved Growth in a Young Infant.

World J Pediatr Congenit Heart Surg 2021 Mar;12(2):284-285

Congenital Cardiac Surgery, Timone Hospital, 369900Assistance Publique-Hôpitaux de Marseille, France.

Surgical repair of Scimitar syndrome is challenging, especially in small patients. Our images demonstrate that the pericardial tunnel technique is feasible even in low-weight patient and that it provides a good growth potential. Read More

View Article and Full-Text PDF

Emergent Lung Resection for Massive Hemoptysis From Bronchial Malformation.

Ann Thorac Surg 2021 12 4;112(6):e423-e426. Epub 2021 Mar 4.

Department of Surgery, Washington University School of Medicine, St Louis, Missouri.

Bronchial arteriovenous malformations are usually asymptomatic findings noted on imaging but may present with massive hemoptysis after endobronchial rupture. Initial treatment usually involves transcatheter embolization with surgery reserved for refractory cases. Here, we present a patient with large-volume hemoptysis after bronchial arteriovenous malformation rupture. Read More

View Article and Full-Text PDF
December 2021

Asymptomatic Large Pulmonary Arteriovenous Malformation Masquerading as a Metastatic Deposit in a Patient with Papillary Thyroid Carcinoma.

Indian J Nucl Med 2020 Oct-Dec;35(4):326-329. Epub 2020 Oct 21.

Department of Nuclear Medicine and Molecular Imaging, Amrita Institute of Medical Sciences and Research Center, Cochin, Kerala, India.

Adult cases of congenital arteriovenous malformation (AVM) of the mediastinum are extremely rare, and because of their varied clinical presentations, they pose a diagnostic challenge. There is no reported association of pulmonary AVM and papillary thyroid carcinoma. We describe a 38-year-old female with a large right lung AVM, multinodular goiter, and high serum thyroglobulin (Tg) with papillary thyroid carcinoma. Read More

View Article and Full-Text PDF
October 2020

Endovascular Repair of Diffuse Pulmonary Arteriovenous Malformations with Systemic Arterial Shunts.

Vasc Endovascular Surg 2021 Aug 24;55(6):642-644. Epub 2021 Feb 24.

Department of Radiological Sciences, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.

Diffuse pulmonary arteriovenous malformations (PAVMs) are defined as arteriovenous malformations (AVMs) involving subsegmental, segmental, or both types of arteries in at least 1 lung lobe and are more extensive than multiple PAVMs. Diffuse PAVMs involving systemic arterial shunts are very rare. We describe a rare case, in which diffuse PAVMs involving systemic arterial shunts were successfully treated with coil embolization. Read More

View Article and Full-Text PDF

Cryptic brain abscess - do not forget hereditary hemorrhagic teleangiectasia!

Am J Hematol 2021 05 11;96(5):640-642. Epub 2021 Feb 11.

Department of Internal Medicine, General Hospital of Šibenik-Knin County, Šibenik, Croatia.

View Article and Full-Text PDF

A rare cause of newborn central cyanosis.

Echocardiography 2020 09 15;37(9):1524-1525. Epub 2020 Aug 15.

Pediatric Cardiology and Congenital Heart Defects Department, Medical University in Gdansk, Gdansk, Poland.

Pulmonary arteriovenous malformations are rare congenital vascular anomalies. They are usually associated with congenital hemorrhagic hemangioma. The hemodynamic effect of fistulas depends on their size, as well as the location. Read More

View Article and Full-Text PDF
September 2020