Bibliografías temáticas / Interstitial lung disease, systemic sclerosis, magnetic resonance imaging, computed tomography

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Literatura académica sobre el tema "Interstitial lung disease, systemic sclerosis, magnetic resonance imaging, computed tomography"

Autor: Grafiati
Publicado: 10 de marzo de 2023
Última modificación: 31 de julio de 2025

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Artículos de revistas sobre el tema "Interstitial lung disease, systemic sclerosis, magnetic resonance imaging, computed tomography"

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Albu, Mihai Tudor, Alexandru-Emil Matei, Jörg H. W. Distler, Frederik L. Giesel, and Yuriko Mori. "Fibroblast activation protein inhibitor PET/CT as an emerging diagnostic modality in interstitial lung disease and other fibrotic conditions." Rheumatology and Immunology Research 5, no. 3 (2024): 152–56. http://dx.doi.org/10.2478/rir-2024-0021.

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Abstract Interstitial lung diseases (ILD) encompass a wide range of disorders characterized by alveolar inflammation and fibrotic tissue remodeling, marked by significant morbidity and mortality. Systemic sclerosis (SSc), among other connective tissue diseases, is a frequent cause of ILD. Assessment of pulmonary fibrosis is frequently constrained by the delayed manifestations of profibrotic activation of fibroblasts, which results in late macroscopic alterations detectable by standard imaging techniques such as computed tomography (CT) and magnetic resonance imaging (MRI) scans. 68Ga-labeled f
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Landini, N., M. Orlandi, M. Occhipinti, et al. "POS0264 THE EMERGING ROLE OF MAGNETIC RESONANCE IMAGING IN INTERSTITIAL LUNG DISEASE IN SYSTEMIC SCLEROSIS: EVIDENCE FOR ULTRA SHORT TE AND COMPRESSED SENSING VIBE ACQUISITIONS AS PROMISING TOOLS FOR THE EVALUATION OF PARENCHYMAL ALTERATIONS." Annals of the Rheumatic Diseases 80, Suppl 1 (2021): 355.1–355. http://dx.doi.org/10.1136/annrheumdis-2021-eular.3253.

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Background:Interstitial lung disease (ILD) is a frequent complication and the major cause of death in Systemic sclerosis (SSc). Computed tomography (CT) is the gold standard imaging technique to assess ILD but is burdened by exposure to ionizing radiations that limits its use for the follow-up. MRI sequences with Ultra Short Echo Time (UTE) are promising for ILD.Objectives:We tested two MRI sequences, UTE Spiral VIBE and Compressing Sensing (CS) VIBE, in SSc-ILD, in comparison to chest CT.Methods:SSc patients with suspected-ascertained ILD were evaluated for undergoing CT-MRI examinations in t
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Orlandi, M., N. Landini, C. Nardi, G. Morana, S. Colagrande, and M. Matucci-Cerinic. "POS0384 ULTRA SHORT ECHO TIME MRI (UTE) SEQUENCE IN THE ASSESSMENT OF INTERSTITIAL DISEASE IN PATIENTS WITH SYSTEMIC SCLEROSIS: CORRELATION WITH DISEASE EXTENSION AT CT AND WITH PULMONARY LUNG FUNCTION TESTS." Annals of the Rheumatic Diseases 81, Suppl 1 (2022): 446.2–447. http://dx.doi.org/10.1136/annrheumdis-2022-eular.4529.

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BackgroundInterstitial lung disease (ILD) is the major cause of death in Systemic sclerosis (SSc). Computed tomography (CT) is the gold standard imaging technique to diagnose ILD and to assess ILD prognosis. ILD extent assessment at lung CT has shown to correlate with functional lung capacity: extensive lung disease (> 20%) correlate with significant lung capacity decline (forced vital capacity ((FVC) <70%) that is, in fact, associated with a higher mortality. Unfortunately, it is burdened by exposure to ionizing radiations that limits its use for the follow-up. For this reason, new MRI
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Shareef, Narin, and Jana Natkunarajah. "CPC08 Two fatal cases of fulminant, rapidly progressive interstitial lung disease secondary to MDA5 dermatomyositis." British Journal of Dermatology 191, Supplement_1 (2024): i11—i12. http://dx.doi.org/10.1093/bjd/ljae090.021.

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Abstract Anti-MDA5 dermatomyositis (DM) is a rare systemic autoimmune condition associated with clinically amyopathic DM and rapidly progressive interstitial lung disease (RP-ILD). It is associated with unique skin features including cutaneous ulceration, eyelid oedema, palmar papules and mechanic’s hands. We present two challenging cases of anti-MDA5 DM with atypical skin manifestations, complicated by RP-ILD, which unfortunately resulted in death in both patients. The first case is a 47-year-old Egyptian woman who initially presented with erythema and burning sensation of the fingertips, thi
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Senkal, N., E. Kiyan, E. Kocasoy-Orhan, et al. "AB0331 PULMONARY INVOLVEMENT IN A SINGLE CENTER COHORT OF PATIENTS WITH SYSTEMIC LUPUS ERYTHEMATOSUS." Annals of the Rheumatic Diseases 80, Suppl 1 (2021): 1191.1–1191. http://dx.doi.org/10.1136/annrheumdis-2021-eular.3152.

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Background:The prevalence of SLE pulmonary involvement varies depending on several factors, including diagnostic methods [1].Objectives:We aimed to determine the frequency of involvement with different diagnostic methods in a single center cohort.Methods:300 SLE patients were included. Chest x-ray (CXR), lung spirometry, carbonmonoxide diffusion test (DLCOc) and echocardiography were performed. High resolution thorax computed tomography (HRCT) was done for a definite diagnosis of interstitial lung disease (ILD) whilst diagram electromyography (EMG), ultrasonography (USG) and magnetic resonance
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Khanna, Dinesh, Oliver Distler, Vincent Cottin, et al. "Diagnosis and monitoring of systemic sclerosis-associated interstitial lung disease using high-resolution computed tomography." Journal of Scleroderma and Related Disorders, January 3, 2022, 239719832110644. http://dx.doi.org/10.1177/23971983211064463.

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Patients with systemic sclerosis are at high risk of developing systemic sclerosis–associated interstitial lung disease. Symptoms and outcomes of systemic sclerosis–associated interstitial lung disease range from subclinical lung involvement to respiratory failure and death. Early and accurate diagnosis of systemic sclerosis–associated interstitial lung disease is therefore important to enable appropriate intervention. The most sensitive and specific way to diagnose systemic sclerosis–associated interstitial lung disease is by high-resolution computed tomography, and experts recommend that hig
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Muscogiuri, Emanuele, Valerie Van Ballaer, Walter De Wever, et al. "Uncommon Causes of Pulmonary Hypertension With Associated Cardiomyopathy: Computed Tomography and Magnetic Resonance Imaging of Cardiothoracic Manifestations." Echocardiography 42, no. 2 (2025). https://doi.org/10.1111/echo.70103.

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ABSTRACTPulmonary hypertension (PH) is a disease characterized by pathologically increased pressure in the pulmonary arteries, defined by a mean pulmonary arterial pressure (mPAP) >20 mmHg at rest measured with right heart catheterization (RHC). This definition encompasses pathologies with very different pathological backgrounds, ultimately resulting in PH. For this reason, the latter can be possibly (though seldom) accompanied by cardiomyopathies, pathologies characterized by a structural and functionally abnormal myocardium not secondary to coronary disease, hypertension, valvular disease
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Pattiata, Cara, and Luke Sammut. "OA15 A case of cardiac manifestation of systemic sclerosis." Rheumatology Advances in Practice 6, Supplement_1 (2022). http://dx.doi.org/10.1093/rap/rkac066.015.

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Abstract Introduction/Background A 45-year-old lady, originally from Peru, with a background of diffuse cutaneous systemic sclerosis presented with shortness of breath on exertion, frequent palpitations, non-exertional chest tightness, and fatigue. Description/Method In 2011, she presented with inflammatory arthritis as well as Raynaud’s phenomenon. Her anti-nuclear antibody screen showed a positive anti-SCL-70 and anti-U3RNP. Over the years she developed pulmonary hypertension, renal involvement (proteinuria), dysphagia, cutaneous involvement (sclerodactyly, digital ulcers, telangiectasia) an
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Lin, Kan-Hsuan, and Jun-Kai Kao. "Overlap syndrome in a 12-year-old girl with systemic lupus erythematosus and anti-oj antibody-positive polymyositis: a case report." Pediatric Rheumatology 20, no. 1 (2022). http://dx.doi.org/10.1186/s12969-022-00753-z.

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Abstract Background The peculiar presentation of overlap syndrome in children makes precise diagnosis difficult. Children with overlap syndrome may or may not have specific antibodies. We present the case of a 12-year-old girl diagnosed with overlap syndrome of systemic lupus erythematosus (SLE) and juvenile polymyositis (JPM) who tested positive for anti-OJ antibodies. Case presentation We describe the case of a 12-year-old girl diagnosed with SLE at the age of 7 and presented with fever with malar rash, periungual erythema, generalized weakness, and multiple joint pain at admission. The pati
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Fontoura Mateus, Nathália Lopes, Paula Velozo Leal, Beatriz Candolo Marques, Karen Fernanda Da Silva, Douglas Rodrigo Mattei, and Elizabeth Regina Carvalho. "Non-Cardiogenic Thromboembolism in a Persian Cat with Hypertrophic Cardiomyopathy." Acta Scientiae Veterinariae 48 (February 13, 2020). http://dx.doi.org/10.22456/1679-9216.100519.

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Background: Hypertrophic cardiomyopathy is the most common acquired cardiovascular disease in the feline species. A frequent complication of this cardiomyopathy is the development of cardiac congestive failure, left atrial enlargement and subsequent development of arterial thromboembolism. In a significant percentage of affected animals there is progression to congestive heart failure, resulting in cyanosis and dyspnea, often the first clinical signs reported by owners. This is a report of a 10-year-old Persian cat with hypertrophic cardiomyopathy and venous and arterial thromboembolism of non
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Tesis sobre el tema "Interstitial lung disease, systemic sclerosis, magnetic resonance imaging, computed tomography"

1

Landini, Nicholas. "Characterization of Connective Tissue Disorders related Interstitial Lung Disease (CTD-ILD) with Computed Tomography (CT) and Magnetic Resonance Imaging (MRI)." Doctoral thesis, 2022. http://hdl.handle.net/2158/1260834.

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Purpose/Objectives Interstitial Lung Disease (ILD) is a major complication of Systemic Sclerosis (SSc), with high morbidity and mortality. Computed tomography is the gold standard for ILD imaging assessment. However, recent Ultra-Short Echo-Time (UTE) Magnetic Resonance Imaging (MRI) sequences are promising for lung parenchyma evaluation. Moreover, different Dynamic Contrast Enhancement (DCE) MRI patterns seems able to identify prevalent inflammatory and fibrotic ILD, with possible implications in the management of the therapy. We aimed to verify the reliability of respiratory triggered UTE S
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Actas de conferencias sobre el tema "Interstitial lung disease, systemic sclerosis, magnetic resonance imaging, computed tomography"

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Assmann, G., M. Schmidt, M. Ramona, et al. "AB1204 COMPARISON OF DIAGNOSTIC SIGNIFICANCE OF HIGH RESOLUTION COMPUTED TOMOGRAPHY (HRCT) AND MAGNET RESONANCE IMAGING (MRI) IN SYSTEMIC SCLEROSIS INTERSTITIAL LUNG DISEASE (SSc-ILD) – A PROSPECTIVE BLINDED MONO-CENTRE STUDY OF 20 CASES." In EULAR 2024 European Congress of Rheumatology, 12-15 June. Vienna, Austria. BMJ Publishing Group Ltd and European League Against Rheumatism, 2024. http://dx.doi.org/10.1136/annrheumdis-2024-eular.3360.

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