Results 81 to 90 of about 112,559 (334)

Case report: Severe dry cough associated with superior vena cava syndrome—Caused recurrent chylothorax

open access: yesFrontiers in Cardiovascular Medicine, 2022
IntroductionSymptomatic pleural effusion is occasionally caused by superior vena cava syndrome. Dyspnea and pleuritic chest pain are common symptoms of pleural effusion.
Ziming Wan
doaj   +1 more source

Prenatal diagnosis and clinical pregnancy outcome of fetuses with conotruncal defects in a Chinese cohort

open access: yesInternational Journal of Gynecology &Obstetrics, EarlyView.
Abstract Objective This study aimed to explore genetic etiologies of conotruncal defects (CTDs) in fetuses by analyzing the results of different genetic tests and to assess pregnancy outcomes of fetuses with CTD in a Chinese prenatal cohort. Methods A total of 146 fetuses that underwent invasive prenatal genetic testing for CTD at the prenatal ...
Min Li   +5 more
wiley   +1 more source

Non-Hodgkin’s Lymphoma Mass Causing Superior Vena Cava Syndrome and Disappeared Completely with Low-dose Steroid: Case Report

open access: yesAnkara Üniversitesi Tıp Fakültesi Mecmuas, 2020
Superior vena cava syndrome is a rare oncologic emergency in children. Non-Hodgkin’s lymphoma is the most common tumor and the most common subtype is T-cell non-Hodgkin’s lymphoma. Steroids, chemotherapy and radiotherapy are used for treatment.
Halil Aslan, Doğan Köse
doaj   +1 more source

Enhanced Feedback Iterative Decoding of Sparse Quantum Codes [PDF]

open access: yesIEEE Transactions on Information Theory 58 (2): 1231-1241 (6 February 2012), 2009
Decoding sparse quantum codes can be accomplished by syndrome-based decoding using a belief propagation (BP) algorithm.We significantly improve this decoding scheme by developing a new feedback adjustment strategy for the standard BP algorithm. In our feedback procedure, we exploit much of the information from stabilizers, not just the syndrome but ...
arxiv   +1 more source

Síndrome de vena cava superior: urgencia oncológica [PDF]

open access: yes, 2018
The first description of superior vena cava syndrome was performed in 1757, by a Scottish physician, William Hunter, in a patient with syphilis aortic aneurysm.
Delgado, Dahiana Delgado
core   +2 more sources

Association Between Fetal Myocardial Alterations and Congenital Heart Disease Based on Post‐Mortem Myocardial MRI

open access: yesiRADIOLOGY, EarlyView.
Applying myocardial parametric mapping based on post‐mortem MRI is feasible for non‐invasive tissue characterization. We speculated that the elevated T2 relaxation may be an essential myocardial tissue characterization of cyanotic congenital heart disease, potentially suggesting myocardial edema, which may provide evidence to guide appropriate ...
Weizeng Zheng   +12 more
wiley   +1 more source

Tratamento da síndrome da veia cava superior Treatment of superior vena cava syndrome

open access: yesJornal Brasileiro de Pneumologia, 2005
A veia cava superior é formada pela união das duas veias inominadas, direita e esquerda, e localiza-se no mediastino médio, à direita da artéria aorta e anteriormente à traquéia.
Luís Marcelo Inaco Cirino   +3 more
doaj   +1 more source

Superior vena caval syndrome caused by the tumor of the left hilum in a patient with unilateral persistent left superior vena cava diagnosed with multislice spiral computed tomography : a case report [PDF]

open access: yes, 2007
Background: Unilateral persistent left superior vena cava (PLSVC) is an infrequent finding with incidence of 18-20% among the individuals with PLSVC. The persistence of the left-sided superior vena cava is an effect of disturbances in development of the ...
Buczkowski, Jarosław   +6 more
core  

Congenital Absence of Superior Vena Cava with no Manifestation of Superior Vena Cava Syndrome [PDF]

open access: yesKorean Circulation Journal, 2016
Total absence of superior vena cava (SVC) is a very rare anomaly, and the patient usually suffers from SVC syndrome or conduction disturbances. We report an asymptomatic 27 year-old male, with complete absence of SVC. Transthoracic echocardiography and computed tomography demonstrated the absence of SVC and other congenital cardiac anomalies, but the ...
Jeong Jae Kim   +3 more
openaire   +3 more sources

Chromosomal Microarray Analysis and Karyotype Analysis for Prenatal Diagnosis of Fetuses With Abnormal Ultrasound Soft Markers

open access: yesJournal of Clinical Laboratory Analysis, EarlyView.
Genetic detection of fetal specimens obtained by ultrasound‐guided puncture was carried out using karyotype analysis and chromosomal microarray analysis (CMA) in this study, and the detection rates of chromosomal abnormalities in different ultrasonic abnormalities were analyzed.
Lina Liu   +4 more
wiley   +1 more source

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