keyword
Keywords coronary syndrome collagen con...

coronary syndrome collagen congenital

https://read.qxmd.com/read/37088677/nephrotic-syndrome-and-acute-coronary-syndrome-in-children-teenagers-and-young-adults-systematic-literature-review
#1
REVIEW
Olivier Wolf, Romain Didier, Frédéric Chagué, Florence Bichat, Luc Rochette, Marianne Zeller, Laurent Fauchier, Bernard Bonnotte, Yves Cottin
Myocardial infarction is rare in children, teenagers and young adults (aged<20 years). The most common aetiologies identified include Kawasaki disease, familial hypercholesterolaemia, collagen vascular disease-induced coronary arteritis, substance abuse (cocaine, glue sniffing), trauma, complications of congenital heart disease surgery, genetic disorders (such as progeria), coronary artery embolism, occult malignancy and several other rare conditions. Nephrotic syndrome is a very rare cause of myocardial infarction, but it is probably underestimated...
May 2023: Archives of Cardiovascular Diseases
https://read.qxmd.com/read/33966639/cardiovascular-magnetic-resonance-in-women-with-cardiovascular-disease-position-statement-from-the-society-for-cardiovascular-magnetic-resonance%C3%A2-scmr
#2
REVIEW
Karen G Ordovas, Lauren A Baldassarre, Chiara Bucciarelli-Ducci, James Carr, Juliano Lara Fernandes, Vanessa M Ferreira, Luba Frank, Sophie Mavrogeni, Ntobeko Ntusi, Ellen Ostenfeld, Purvi Parwani, Alessia Pepe, Subha V Raman, Hajime Sakuma, Jeanette Schulz-Menger, Lilia M Sierra-Galan, Anne Marie Valente, Monvadi B Srichai
This document is a position statement from the Society for Cardiovascular Magnetic Resonance (SCMR) on recommendations for clinical utilization of cardiovascular magnetic resonance (CMR) in women with cardiovascular disease. The document was prepared by the SCMR Consensus Group on CMR Imaging for Female Patients with Cardiovascular Disease and endorsed by the SCMR Publications Committee and SCMR Executive Committee. The goals of this document are to (1) guide the informed selection of cardiovascular imaging methods, (2) inform clinical decision-making, (3) educate stakeholders on the advantages of CMR in specific clinical scenarios, and (4) empower patients with clinical evidence to participate in their clinical care...
May 10, 2021: Journal of Cardiovascular Magnetic Resonance
https://read.qxmd.com/read/15590083/the-coronary-circulation-in-cyanotic-congenital-heart-disease
#3
JOURNAL ARTICLE
Joseph K Perloff
BACKGROUND: Dilated coronary arteries, coronary blood flow, and the paucity of coronary atherosclerosis have not been studied in cyanotic congenital heart disease. METHODS: Coronary arteriograms were interpreted in 59 cyanotic adults, and dilated coronaries were examined histologically in 6. Coronary blood flow was determined with N-13 ammonia positron emission tomography in 14 Eisenmenger syndrome patients and in 10 controls. Total non-fasting cholesterols were retrieved in 279 patients who were divided into: Group A--143 cyanotic unoperated, Group B--47 acyanotic after operation, Group C--41 acyanotic unoperated, Group D--48 acyanotic before and after operation...
December 2004: International Journal of Cardiology
https://read.qxmd.com/read/11523694/matrix-metalloproteinases-from-biology-to-therapeutic-strategies-in-cardiovascular-disease
#4
REVIEW
I J Benjamin
In this comprehensive review of matrix remodeling, one central theme that bears re-emphasis is the extensivecross-talk and dynamic interactions that exist between terminally differentiated, postmitotic cells, proliferative cells, and the ECM of the cardiovascular system. The activities of MMPs and TIMPs constitute a well-orchestrated contest to maintain tissue integrity and homeostasis. Overexpression of MMPs tilts the balance in favor of irreversible tissue destruction of joints (eg, as in rheumatic disease), and efforts to curtail such errant pathways are ongoing (123)...
September 2001: Journal of Investigative Medicine: the Official Publication of the American Federation for Clinical Research
https://read.qxmd.com/read/11343993/pathology-of-the-diffuse-variant-of-supravalvar-aortic-stenosis
#5
JOURNAL ARTICLE
P Vaideeswar, V Shankar, J R Deshpande, A Sivaraman, N Jain
Supravalvar aortic stenosis is a rare congenital heart anomaly, producing left ventricular outflow tract obstruction. Of the two anatomic variants that have been described, diffuse type is the rarest. We report five such cases in children between two months and nine years of age. None had features of Williams syndrome. The entire aorta was involved in three cases, with abdominal aortic coarctation in two cases. Stenosis was mainly due to involvement of the media, which showed smooth muscle hypertrophy, abnormal elastic fibers, and mild collagenization...
January 2001: Cardiovascular Pathology: the Official Journal of the Society for Cardiovascular Pathology
https://read.qxmd.com/read/7967668/cardiac-fibroma-clinicopathologic-correlates-and-surgical-treatment
#6
JOURNAL ARTICLE
A P Burke, M Rosado-de-Christenson, P A Templeton, R Virmani
The clinicopathologic findings of 23 patients with cardiac fibroma are presented. The mean patient age was 13 years, with a range of 1 day to 56 years. The presenting symptoms included heart failure, arrhythmias, sudden death, cyanosis, and chest pain. Some patients had no symptoms, and one patient had Gorlin's syndrome. Echocardiography and magnetic resonance imaging were very sensitive in diagnosis. Nineteen patients underwent tumor resection or biopsy, and four tumors were diagnosed at cardiac transplantation or autopsy on explanted hearts...
November 1994: Journal of Thoracic and Cardiovascular Surgery
https://read.qxmd.com/read/6029164/heart-block-and-coronary-artery-disease
#7
JOURNAL ARTICLE
M J Davies, D Redwood, A Harris
No abstract text is available yet for this article.
August 5, 1967: British Medical Journal (1857-1980)
https://read.qxmd.com/read/1171679/-arteriopathia-calcificans-infantum
#8
JOURNAL ARTICLE
M Stolte, B Jurowich
A report is given on all 11-weeek-old male child who, after normal development, suddenly became critically ill and died within 8 hours. The autopsy revealed a rare aetiologically and in its pathogenesis unclarified, always lethal clinical picture of so-called "Arteriopathia calcificans infantum" (ACI). An analysis of 90 published cases revealed an average age of the diseased children of 150.9 days and a mean duration of the disease of 32.8 days; in the large majority of the cases (64.7%), death occurred at the latest within 3 days of the first symptoms...
May 1975: Basic Research in Cardiology
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