The main presenting clinical manifestations were congestive heart failure in 10 of the 32 patients (31%), distal atrioventricular block in 10 patients (31%), sustained VT in 7 cases (22%), and a syndrome mimicking acute myocardial infarction with chest pain and ST-segment changes in 4 cases (13%). Myocarditis can affect your heart muscle and your heart's electrical system, reducing your heart's ability to pump and causing rapid or abnormal heart rhythms (arrhythmias).A viral infection usually causes myocarditis, but it can result from a reaction to a drug or be part of a more general inflammatory condition. The mean ejection fraction was 38±13% with values <50% in 23 patients (74%). TTE showed improved contractility with an EF of 45%.
For this reason, giant cell arteritis is sometimes called temporal arteritis.Giant cell arteritis frequently causes headaches, scalp tenderness, jaw pain and vision problems. Spontaneous echocontrast or "smoke" can be seen in the left ventricle due to low flow and stasis.Copyright © 2015 Rose Tompkins et al. We set out to analyze (1) our experience in diagnosing giant-cell myocarditis and (2) the outcome of patients on combined immunosuppression.We reviewed the histories, diagnostic procedures, details of treatment, and outcome of 32 consecutive patients with histologically verified giant-cell myocarditis treated in our hospital since 1991. ×40).Giant Cell Myocarditis: Not Always a Presentation of Cardiogenic ShockDepartment of Cardiology, New York University Langone Medical Center, New York, NY 10016, USADepartment of Radiology, New York University School of Medicine, New York, NY 10016, USA Giant cell myocarditis in an explant heart from patient. The diagnosis is based on endomyocardial biopsy. Earlier reports have shown that if left untreated, giant-cell myocarditis is often fatal. Combined immunosuppression with corticosteroids and calcineurin inhibitor resulted in resolution of symptoms and sustained recovery of left ventricular function one year later. The Multicenter GCM Study Group also initially required absence of granulomas for the diagnosis of GCMThe 1997 report by the Multicenter GCM Study Group established the gloomy prognosis of the disease: out of 63 patients, 89% either died or underwent transplantation with a median transplant-free survival of only 5.5 months from symptom onset.There are no good data to guide immunosuppression for long-term maintenance of remission in GCM. Although the outlook of GCM on combined immunosuppression thus looks less grim than usually thought the present data are at best suggestive and there remain many deficiencies in our knowledge about GCM. Of the 32 cases, 26 were diagnosed by endomyocardial biopsies (EMBs [n=23]) or surgical biopsies (n=3), 4 at autopsy, and 2 from explanted hearts post-transplantation. Correspondence to Jukka Lehtonen, MD, Division of Cardiology, Helsinki University Central Hospital, 00029 Helsinki, Finland. The data are median and range. Giant cell myocarditis (GCM) is a rare and often fatal disease with the most obvious presentation being a rapid hemodynamic deterioration with declining left ventricular (LV) systolic function and cardiogenic shock .
A clinically worthwhile observation was also the high frequency of atrioventricular block as the first manifestation of the disease, equaling the frequency of heart failure at hospital presentation.With 32 patients ours is by far the largest series of GCM reported from a single institution. Giant cell myocarditis was confirmed via endomyocardial biopsy. Since the first report of the Multicenter GCM Study Group,We initially identified from the medical records 36 patients with GCM, the diagnoses having been made by pathologists in the referring hospitals (n=18) or at our institution (n=18). Nine patients with ventricular tachycardia (VT) have been reported previouslyFrom 1991 through 2005, we were routinely using clinical examination, 12-lead ECG, laboratory tests, and echocardiography to explore the pathogenesis of an unknown myocardial disease. Introduction. The most obvious presentation often described in the literature is one of rapid hemodynamic deterioration due to cardiogenic shock necessitating urgent consideration of mechanical circulatory support and heart transplantation. Twenty-one patients (68%) had locally thinned or thickened interventricular septum and 3 (10%) had aneurysms of the left ventricle (Contrast-enhanced cardiac MRI was done in 9 patients and showed areas of late contrast enhancement in each. The median follow-up time calculated from symptom onset was 15.0 months (range, 0.3–90.3 months). Early diagnosis is critical, as recent studies have shown that rapidly instituted cyclosporine-based immunosuppression can reduce inflammation and improve transplant-free survival. Data presented as number of patients or median and range. However, our understanding of the disease is still developing.
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