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3.
Catheter Cardiovasc Interv ; 99(5): 1558-1562, 2022 04.
Article in English | MEDLINE | ID: covidwho-1850011

ABSTRACT

We report the first use of a single 100-mm long custom-made version of the Optimus-CVS® balloon-expandable PTFE-covered XXL (15-Zig) stent (AndraTec, GmbH) to eliminate sinus venosus defect left-to-right shunt and redirect anomalous right pulmonary veins blood flow through a new walled channel to the left atrium. Anatomical feasibility and strategy decision were guided by ex-vivo procedure simulation on the patient-specific 3D printed heart model and in-vivo balloon interrogation. Modified procedural and implantation techniques are detailed. Immediate and one-month follow-up showed excellent outcomes.


Subject(s)
Heart Defects, Congenital , Heart Septal Defects, Atrial , Pulmonary Veins , Vascular Malformations , Drainage , Humans , Pulmonary Veins/abnormalities , Pulmonary Veins/diagnostic imaging , Pulmonary Veins/surgery , Stents , Treatment Outcome
4.
J Stroke Cerebrovasc Dis ; 31(5): 106353, 2022 May.
Article in English | MEDLINE | ID: covidwho-1712840

ABSTRACT

Stroke is a common and devastating event and the majority of cases are caused by thromboembolism from the left atrium, left ventricle or left sided valves. This case report describes a case of embolic stroke with the origin of the thrombus from the left inferior pulmonary vein. The importance of this case is twofold. Firstly, it is the fourth case report of pulmonary venous thrombosis, a very rare condition, due to COVID-19 infection and secondly, it focuses attention on the fact that the left atrium is not the most proximal address of arterial thromboembolism-the pulmonary veins are. Thus, it is proposed that a thorough assessment of the pulmonary veins should be done in all cases of arterial thromboembolism.


Subject(s)
COVID-19 , Embolic Stroke , Ischemic Stroke , Pulmonary Embolism , Pulmonary Veins , Thromboembolism , Venous Thrombosis , COVID-19/complications , Embolic Stroke/diagnostic imaging , Embolic Stroke/etiology , Humans , Pulmonary Embolism/etiology , Thromboembolism/complications , Venous Thrombosis/complications
6.
Chest ; 159(6): e361-e364, 2021 06.
Article in English | MEDLINE | ID: covidwho-1241747

ABSTRACT

Research on COVID-19, the cause of a rapidly worsening pandemic, has led to the observation of laboratory derangements such as a propensity towards a hypercoagulable state. However, there are currently no reports on the incidence of pulmonary venous thrombosis in the setting of COVID-19. We report a case in which follow-up chest CT scans revealed an expansile filling defect in a branch of the right inferior pulmonary vein, which is consistent with pulmonary venous thrombosis. Our objective was to provide insight into an uncommon sequela of COVID-19 and consequently garner increased clinical suspicion for pulmonary VTE during hospitalization.


Subject(s)
COVID-19/complications , Pulmonary Veins , Venous Thrombosis/diagnosis , Venous Thrombosis/virology , Adult , COVID-19/diagnosis , COVID-19/therapy , Humans , Male , Tomography, X-Ray Computed , Venous Thrombosis/therapy
7.
Medicina (Kaunas) ; 57(4)2021 Mar 24.
Article in English | MEDLINE | ID: covidwho-1154448

ABSTRACT

Background: Establishing the diagnosis of COVID-19 and Pneumocystisjirovecii pulmonary coinfection is difficult due to clinical and radiological similarities that exist between the two disorders. For the moment, fungal coinfections are underestimated in COVID-19 patients. Case presentation: We report the case of a 52-year-old male patient, who presented to the emergency department for severe dyspnea and died 17 h later. The RT-PCR test performed at his admission was negative for SARS-CoV-2. Retesting of lung fragments collected during autopsy revealed a positive result for SARS-CoV-2. Histopathological examination showed preexisting lesions, due to comorbidities, as well as recent lesions: massive lung thromboses, alveolar exudate rich in foam cells, suprapleural and intra-alveolar Pneumocystisjirovecii cystic forms, and bilateral adrenal hemorrhage. Conclusion: COVID-19 and P.jirovecii coinfection should be considered, particularly in critically ill patients, and we recommend the systematic search for P. jirovecii in respiratory samples.


Subject(s)
COVID-19/pathology , Lung/pathology , Pneumonia, Pneumocystis/pathology , Respiratory Insufficiency/pathology , Thrombosis/pathology , Acute Kidney Injury/complications , Acute-On-Chronic Liver Failure/complications , Adrenal Gland Diseases/complications , Adrenal Gland Diseases/pathology , Autopsy , COVID-19/complications , Coinfection/pathology , Exudates and Transudates , Fatal Outcome , Fibrosis , Foam Cells/pathology , Hemorrhage/complications , Hemorrhage/pathology , Humans , Hypertension/complications , Liver Diseases, Alcoholic/complications , Male , Middle Aged , Myocardial Ischemia/complications , Pneumonia, Pneumocystis/complications , Pulmonary Artery/pathology , Pulmonary Veins/pathology , Respiratory Insufficiency/etiology , SARS-CoV-2 , Thrombosis/etiology
8.
Eur J Radiol ; 134: 109442, 2021 Jan.
Article in English | MEDLINE | ID: covidwho-1060223

ABSTRACT

PURPOSE: The vascular enlargement (VE) pattern differs from previously described imaging patterns for pneumonia. This study aimed to investigate the incidence, computed tomography (CT) characteristics, and diagnostic value of the VE pattern in coronavirus disease 2019 (COVID-19). METHOD: The CT data of 106 patients with COVID-19 from January 19 to February 29, 2020, and 52 patients with influenza virus pneumonia (IVP) from January 2018 to February 2020 were retrospectively collected. The incidences of the VE pattern between the two groups were compared. The CT manifestations of COVID-19 were analyzed with a particular focus on the VE pattern's specific CT signs, dynamic changes, and relationships with lesion size and disease severity. RESULTS: Peripheral and multilobar ground-glass opacities (GGOs) or mixed GGOs with various sizes and morphologies were typical features of COVID-19 on initial CT. The VE pattern was more common in COVID-19 (88/106, 83.02 %) than in IVP (10/52, 19.23 %) on initial CT (P < 0.001). Three special VE-pattern-specific CT signs, including central vascular sign, ginkgo leaf sign, and comb sign, were identified. Four types of dynamic changes in the VE pattern were observed on initial and follow-up CT, which were closely associated with the evolution of lesions and the time interval from the onset of symptoms to initial CT scan. The VE pattern in COVID-19 was more commonly seen in larger lesions and patients with severe-critical type (all P < 0.001). CONCLUSIONS: The VE pattern is a valuable CT sign for differentiating COVID-19 from IVP, which correlates with more extensive or serious disease. A good understanding of the CT characteristics of the VE pattern may contribute to the early and accurate diagnosis of COVID-19 and prediction of the evolution of lesions.


Subject(s)
COVID-19/diagnostic imaging , Lung/diagnostic imaging , Pneumonia/diagnostic imaging , Pulmonary Artery/pathology , Pulmonary Veins/diagnostic imaging , Pulmonary Veins/pathology , Tomography, X-Ray Computed/methods , Adolescent , Adult , Aged , Aged, 80 and over , COVID-19/pathology , Child , Diagnosis, Differential , Female , Humans , Influenza, Human/diagnostic imaging , Influenza, Human/pathology , Lung/blood supply , Lung/pathology , Male , Middle Aged , Pneumonia/pathology , Pulmonary Artery/diagnostic imaging , Retrospective Studies , SARS-CoV-2 , Young Adult
9.
Br J Radiol ; 94(1118): 20200716, 2021 Feb 01.
Article in English | MEDLINE | ID: covidwho-1038510

ABSTRACT

OBJECTIVES: Ground-glass opacity and consolidation are recognized typical features of Coronavirus disease-19 (COVID-19) pneumonia on Chest CT, yet ancillary findings have not been fully described. We aimed to describe ancillary findings of COVID-19 pneumonia on CT, to define their prevalence, and investigate their association with clinical data. METHODS: We retrospectively reviewed our CT chest cases with coupled reverse transcriptase polymerase chain reaction (rt-PCR). Patients with negative rt-PCR or without admission chest CT were excluded. Ancillary findings included: vessel enlargement, subpleural curvilinear lines, dependent subpleural atelectasis, centrilobular solid nodules, pleural and/or pericardial effusions, enlarged mediastinal lymph nodes. Continuous data were expressed as median and 95% confidence interval (95% CI) and tested by Mann-Whitney U test. RESULTS: Ancillary findings were represented by 106/252 (42.1%, 36.1 to 48.2) vessel enlargement, 50/252 (19.8%, 15.4 to 25.2) subpleural curvilinear lines, 26/252 (10.1%, 7.1 to 14.7) dependent subpleural atelectasis, 15/252 (5.9%, 3.6 to 9.6) pleural effusion, 15/252 (5.9%, 3.6 to 9.6) mediastinal lymph nodes enlargement, 13/252 (5.2%, 3 to 8.6) centrilobular solid nodules, and 6/252 (2.4%, 1.1 to 5.1) pericardial effusion. Air space disease was more extensive in patients with vessel enlargement or centrilobular solid nodules (p < 0.001). Vessel enlargement was associated with longer history of fever (p = 0.035) and lower admission oxygen saturation (p = 0.014); dependent subpleural atelectasis with lower oxygen saturation (p < 0.001) and higher respiratory rate (p < 0.001); mediastinal lymph nodes with shorter history of cough (p = 0.046); centrilobular solid nodules with lower prevalence of cough (p = 0.023), lower oxygen saturation (p < 0.001), and higher respiratory rate (p = 0.032), and pericardial effusion with shorter history of cough (p = 0.015). Ancillary findings associated with longer hospital stay were subpleural curvilinear lines (p = 0.02), whereas centrilobular solid nodules were associated with higher rate of intensive care unit admission (p = 0.01). CONCLUSION: Typical high-resolution CT findings of COVID-19 pneumonia are frequently associated with ancillary findings that variably associate with disease extent, clinical parameters, and disease severity. ADVANCES IN KNOWLEDGE: Ancillary findings might reflect the broad range of heterogeneous mechanisms in severe acute respiratory syndrome from viral pneumonia, and potentially help disease phenotyping.


Subject(s)
COVID-19/diagnostic imaging , Incidental Findings , Lung/diagnostic imaging , SARS-CoV-2 , Adult , Aged , Aged, 80 and over , Dilatation, Pathologic/diagnostic imaging , Female , Humans , Lung/blood supply , Lymph Nodes/diagnostic imaging , Lymphadenopathy/diagnostic imaging , Male , Middle Aged , Multidetector Computed Tomography/methods , Observer Variation , Pleural Effusion/diagnostic imaging , Pulmonary Artery/diagnostic imaging , Pulmonary Veins/diagnostic imaging , Retrospective Studies
10.
BMJ Case Rep ; 14(1)2021 Jan 08.
Article in English | MEDLINE | ID: covidwho-1015619

ABSTRACT

Hereditary haemorrhagic telangiectasia (HHT) also known as Osler-Weber-Rendu syndrome is an autosomal dominant disorder affecting 1 in 8000 individuals. The eponym recognises the 19th-century physicians William Osler, Henri Jules Louis Marie Rendu and Frederick Parkes Weber who each independently described the disease. It is characterised by epistaxis, telangiectasia and visceral arteriovenous malformations. Individuals with HHT have been found to have abnormal plasma concentrations of transforming growth factor beta and vascular endothelial growth factor secondary to mutations in ENG, ACVRL1 and MADH4. Pulmonary artery malformations (PAVMs) are abnormal communications between pulmonary arteries and veins and are found in up to 50% of individuals with HHT. The clinical features suggestive of PAVMs are stigmata of right to left shunting such as dyspnoea, hypoxaemia, cyanosis, cerebral embolism and unexplained haemoptysis or haemothorax. The authors present the case of a 33-year-old woman presenting with progressive dyspnoea during the COVID-19 pandemic. She had a typical presentation of HHT with recurrent epistaxis, telangiectasia and pulmonary arteriovenous malformations. Although rare, PAVM should be considered in individuals presenting to the emergency department with dyspnoea and hypoxaemia. Delayed diagnosis can result in fatal embolic and haemorrhagic complications.


Subject(s)
Arteriovenous Malformations/diagnosis , Dyspnea/physiopathology , Epistaxis/physiopathology , Hypoxia/physiopathology , Telangiectasia, Hereditary Hemorrhagic/diagnosis , Activin Receptors, Type II/genetics , Adult , Antithyroid Agents/therapeutic use , Arteriovenous Malformations/physiopathology , Blood Gas Analysis , COVID-19/diagnosis , Carbimazole/therapeutic use , Diagnosis, Differential , Female , Graves Disease/complications , Graves Disease/drug therapy , Humans , Migraine Disorders/complications , Pulmonary Artery/abnormalities , Pulmonary Artery/diagnostic imaging , Pulmonary Veins/abnormalities , Pulmonary Veins/diagnostic imaging , SARS-CoV-2 , Telangiectasia, Hereditary Hemorrhagic/complications , Telangiectasia, Hereditary Hemorrhagic/physiopathology , Tomography, X-Ray Computed
15.
Clin Appl Thromb Hemost ; 26: 1076029620936350, 2020.
Article in English | MEDLINE | ID: covidwho-639157

ABSTRACT

This practical guidance, endorsed by the Brazilian Society of Thrombosis and Hemostasis and The Brazilian Society of Angiology and Vascular Surgery, the International Union of Angiology and the European Venous Forum, aims to provide physicians with clear guidance, based on current best evidence-based data, on clinical strategies to manage antithrombotic strategies in patients with coronavirus disease 2019.


Subject(s)
Betacoronavirus , Coronavirus Infections/complications , Pandemics , Pneumonia, Viral/complications , Practice Guidelines as Topic , Thrombophilia/therapy , Thrombosis/prevention & control , Anticoagulants/therapeutic use , Biomarkers , COVID-19 , Clinical Trials as Topic , Coronavirus Infections/blood , Cytokine Release Syndrome/blood , Cytokine Release Syndrome/etiology , Disease Management , Endothelium, Vascular/physiopathology , Endothelium, Vascular/virology , Evidence-Based Medicine , Fibrin Fibrinogen Degradation Products/analysis , Humans , Lung Diseases/etiology , Lung Diseases/prevention & control , Pneumonia, Viral/blood , Pulmonary Veins , SARS-CoV-2 , Thrombophilia/etiology , Thrombophlebitis/etiology , Thrombophlebitis/prevention & control , Thrombosis/etiology , Venous Thromboembolism/etiology , Venous Thromboembolism/prevention & control
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