Zobrazeno 1 - 10
of 988
pro vyhledávání: '"Myxomas"'
Publikováno v:
The Egyptian Heart Journal, Vol 76, Iss 1, Pp 1-6 (2024)
Abstract Background Primary cardiac tumors are uncommon, with approximately 70–80% classified as benign. Myxomas constitute roughly half of all benign cardiac tumors, while cardiac hydatid cysts are exceptionally rare. Shortness of breath is a prom
Externí odkaz:
https://doaj.org/article/2ceb60f9b2ac444b9fe05f9df62ed858
Autor:
Cheng Cheng, Yang Song, Haidong Yan, Daojun Bao, Xiaodi Zhang, Yi Zhao, Daxing Liu, Dengshen Zhang
Publikováno v:
BMC Cardiovascular Disorders, Vol 24, Iss 1, Pp 1-8 (2024)
Abstract Background Carney syndrome is an uncommon autosomal disorder closely linked to mutations in the PRKAR1A gene. Skin lesions are the most pronounced feature of Carney syndrome, affecting over 80% of individuals with this condition. This syndro
Externí odkaz:
https://doaj.org/article/cabb4604fed9490f8b2fdb4a9ee3b0cc
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2024)
Cardiac myxoma is a rare etiology of ischemic stroke, especially in young people. We report a case of multiple myxomas in left atrium and right ventricle inducing acute cerebral infarction. No significant abnormalities were detected in the patient's
Externí odkaz:
https://doaj.org/article/ad4090038c444379b74f6a847efc2706
Autor:
Laurys Boudin, Valeria De Luca, Léna Mescam-Mancini, Vincent Niziers, Delphine Perrot, Jerome Guiramand, Audrey Monneur, Christophe Chagnaud, François Bertucci
Publikováno v:
Case Reports in Oncology, Vol 16, Iss 1, Pp 294-301 (2023)
The Mazabraud syndrome is a rare form of bone fibrous dysplasia associated with intramuscular myxomas. The McCune-Albright syndrome is characterized by the association of dysplasia fibrous bone to one or more extra-osseous manifestations, including c
Externí odkaz:
https://doaj.org/article/dddd8d1a45564fe8b07cf1f1162aae7d
Publikováno v:
BMC Cardiovascular Disorders, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Background Primary cardiac tumors are rare, and cardiac myxoma (CM) accounts for the majority of these tumors. Most of the reports in the literature are case reports. This study summarizes our clinical experience in the surgical treatment of
Externí odkaz:
https://doaj.org/article/732fc452f7914559840a3e2053a23e49
Autor:
Bandar Alamro, Valeria Pergola, Abdalla Eltayeb, Amal Alshammari, Naji Kholaif, Ahmad Alhamshari, Mohammed Al Admawi, Shamayel Mohammed, Feras Khaliel, Domenico Galzerano
Publikováno v:
Monaldi Archives for Chest Disease (2023)
Nowadays, the diagnosis of cardiac myxomas (CM), particularly the histological types, remains a challenge. Two-dimensional (2D) transthoracic (TT) and transesophageal (TEE) echocardiography (ECHO) represent the first steps in the imaging pathway. 3D
Externí odkaz:
https://doaj.org/article/2117de896aca4df69983d28ed2fb9d76
Autor:
Akshay Mathavan, Akash Mathavan, Urszula Krekora, Mohit Mathavan, Vanessa Rodriguez, Ellery Altshuler, Brianna Nguyen, Mohammed Ruzieh
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundPrimary cardiac tumors are often benign and commonly present as cardiac myxomas (CMs) or papillary fibroelastomas (CPFEs). There is a paucity of prognostic indicators for tumor burden or potential for embolic cerebrovascular events (CVEs).
Externí odkaz:
https://doaj.org/article/7a7443d1ca624719bdc64ed930a49a26
Autor:
Ahmed Abdulfattah Alhasso, Okba F. Ahmed, Dana H. Mohammed-Saeed, Fahmi H. Kakamad, Saif S. Almodhaffer, Zaid A. Zaid, Hiwa O. Abdullah, Razhan K. Ali, Suhaib H. Kakamad, Diyar A. Omar, Berun A. Abdalla, Shvan H. Mohammed, Mohammed Q. Mustafa
Publikováno v:
Frontiers in Surgery, Vol 10 (2023)
BackgroundCardiac myxoma is a rare cardiac tumor that may be asymptomatic or can cause embolization or intracardiac obstruction, leading to heart failure, sudden cardiac death, and arrhythmia. This study aims to report an 11-year experience of a sing
Externí odkaz:
https://doaj.org/article/c8885ea72dd844d7943c14c823286f55
Publikováno v:
Iatreia, Vol 35, Iss 2, Pp 183-192 (2022)
Carney complex is a disease characterized by skin lesions, endocrine, cardiac, gonadal and other organ tumors, associated with mutations of the PRKAR1A gene. We present the clinical case of a patient with several of the most characteristic manifestat
Externí odkaz:
https://doaj.org/article/e5b14cc57f0549508bbc1f03de83fadb
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.