Results 41 to 50 of about 7,444 (195)

Biventricular Intravascular Microaxial Blood Pumps and Immunosuppression as a Bridge to Recovery in Giant Cell Myocarditis

open access: yesJACC: Case Reports, 2020
We report a case of giant cell myocarditis in a 76-year-old patient managed with combined immunosuppression and biventricular intravascular microaxial blood pumps. This case highlights a feasible approach for managing such patients who are not candidates
Janet I. Ma, MD   +3 more
doaj   +1 more source

Idiopathic systemic granulomatous pathology causing sudden death due to myocarditis: A rare case report

open access: yesIndian Journal of Pathology and Microbiology, 2015
Idiopathic granulomatous myocarditis is extremely rare, particularly since the introduction of drugs effective against tuberculosis (TB), viruses, fungi and the effective treatment of sarcoidosis.
Harpal Singh, Ramesh Kundal
doaj   +1 more source

Left Atrial Giant Cell Myocarditis Presenting as a Tumor: First-in-Man Case Report

open access: yesBrazilian Journal of Cardiovascular Surgery
Giant cell myocarditis is a rare and highly lethal disorder with resultant cardiac insufficiency. It necessitates aggressive immune suppression therapy, although the results are often fatal.
Omer Tanyeli   +3 more
doaj   +1 more source

Clinical case of the treatment of acute heart failure with extracorporeal membrane oxygenation in patients with acute idiopathic giant cell myocarditis [PDF]

open access: yesКардіохірургія та інтервенційна кардіологія, 2016
The article describes clinical case demonstrating the feasibility of using extracorporeal circulatory support in patients with severe heart failure caused by idiopathic giant cell myocarditis.
B.M. Todurov   +6 more
doaj  

Progressive Thinning of the Basal Interventricular Septum by Giant Cell Myocarditis

open access: yesJACC: Case Reports, 2020
We describe a patient with ventricular tachycardia and complete atrioventricular block. Remarkable thinning of the basal interventricular septum preceded left ventricular dysfunction. Endomyocardial biopsy demonstrated giant cell myocarditis. The patient
Arthur Iturriagagoitia, MD   +5 more
doaj   +1 more source

Cardiovascular involvement in Kawaski Disease [PDF]

open access: yes, 2005
This article contains a case report of a 19 month old child with Kawasaki Disease who developed bilateral giant coronary artery aneurysms.peer ...
Chintala, Kavitha   +2 more
core  

Fulminantne müokardiit. Haigusjuht ja kirjanduse ülevaade [PDF]

open access: yes, 2018
Müokardiit on heterogeenne haigus nii etioloogia kui ka kliinilise kulu poolest. Haiguse aluseks on põletikuline südamelihase kahjustus, mis kulgeb ägeda, enamasti taaspöörduva sündroomina.
Altmets, Mait   +5 more
core   +2 more sources

Idiopathic giant cell myocarditis in a newborn: case report

open access: yesThe Turkish Journal of Pediatrics, 2016
Idiopathic giant cell myocarditis (IGCM) is a rare cause of arrhythmia, heart failure and death in children. The etiology of IGCM is unknown. Endomyocardial biopsy and histological examination are essential for diagnosis.
Doğuş Özdemir-Kara   +5 more
doaj   +1 more source

Regulatory lymphoid and myeloid cells determine the cardiac immunopathogenesis of Trypanosoma cruzi infection [PDF]

open access: yes, 2018
Chagas disease is a multisystemic disorder caused by the protozoan parasite Trypanosoma cruzi, which affects ~8 million people in Latin America, killing 7,000 people annually.
Abrahamsohn   +94 more
core   +3 more sources

Histopathological Evaluation of Somatostatin Receptor 2 Expression in Myocarditis—Rationale for the Diagnostic Use of Somatostatin Receptor Imaging

open access: yesDiagnostics
Background/Objectives: Myocarditis is an inflammatory disease of the myocardium and remains to this day a challenging diagnosis. A promising novel imaging method uses the expression of somatostatin receptors (SSTRs) on inflammatory cells to visualize ...
Christian L. Polte   +10 more
doaj   +1 more source

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