Andrea Frustaci
Catholic University of the Sacred Heart
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Circulation | 1997
Andrea Frustaci; Cristina Chimenti; Fulvio Bellocci; Emanuela Morgante; M. A. Russo; Attilio Maseri
BACKGROUND Lone atrial fibrillation (LAF) is a common clinical syndrome, but its origin remains unknown. METHODS AND RESULTS We performed endomyocardial biopsies of the right atrial septum (2 to 3 per patient; mean, 2.8) and of the two ventricles (6 per patient) in 12 patients (10 men, 2 women; mean age, 32 years) with paroxysmal LAF refractory to conventional antiarrhythmic treatment. As controls, we used endomyocardial biopsies (3 to 5 per patient; mean, 4.4) from the right atrial septum of 11 patients with Wolff-Parkinson-White syndrome (WPW) undergoing resection of the abnormal AV pathway. The weight of the biopsies ranged from 2.8 to 4.5 mg. Biopsy samples were processed for histology and electron microscopy and were read by a pathologist blinded to clinical data. All patients underwent two-dimensional Doppler echocardiography; cardiac catheterization; coronary angiography; and hormonal, virologic, and electrophysiological studies. All tests and WPW biopsies were normal, but all LAF atrial biopsy specimens (average, 2.8 per patient) showed abnormalities (P<.0001). The type of abnormalities varied: Two patients had a severe hypertrophy with vacuolar degeneration of the atrial myocytes and ultrastructural evidence of fibrillolysis occupying >50% of the areas assessed morphometrically (P=.50), 8 had lymphomononuclear infiltrates with necrosis of the adjacent myocytes (5 with fibrosis and 3 without; P<.003), and 2 had only nonspecific patchy fibrosis (P=.50). Biventricular biopsies were abnormal in only 3 patients and showed inflammatory infiltrates similar to those found in atrial biopsies. CONCLUSIONS Abnormal atrial histology was uniformly found in multiple biopsy specimens in all patients with LAF. It was compatible with a diagnosis of myocarditis in 66% of patients (active in 25%) and of noninflammatory localized cardiomyopathy in 17% and was represented by patchy fibrosis in 17%. The cause of the pathological changes, which were found only in atrial septal biopsies but not in biventricular biopsies, in 75% of patients remains unknown.
Chest | 1998
Paolo Zeppilli; Antonio Dello Russo; Cesare Santini; Vincenzo Palmieri; Luigi Natale; Alessandro Giordano; Andrea Frustaci
Biochemical and Biophysical Research Communications | 2003
Luisa Nanni; Maurizio Pieroni; Cristina Chimenti; Barbara Simionati; Rosanna Zimbello; Attilio Maseri; Andrea Frustaci; Gerolamo Lanfranchi
Chest | 1998
Andrea Frustaci; Nicola Gentiloni; Cristina Chimenti; Luigi Natale; Giovanni Gasbarrini; Attilio Maseri
Chest | 1994
Paolo Zeppilli; Cesare Santini; Vincenzo Palmieri; Roberto Vannicelli; Alessandro Giordano; Andrea Frustaci
Chest | 1995
Andrea Frustaci; Sergio Cameli; Paolo Zeppilli
International Journal of Sports Medicine | 1997
Paolo Zeppilli; Cesare Santini; S. Cameli; A. Dello Russo; C. Picani; Alessandro Giordano; Andrea Frustaci
Chest | 1997
Andrea Frustaci; Cristina Chimenti; Maurizio Pieroni
Chest | 1982
Andrea Frustaci; A.C. Rebuzzi; Giovanni Schiavoni; E. Coppola; U. Manzoli
Annals of the New York Academy of Sciences | 1995
Andrea Frustaci; A. Zurlo; Giulietta A. Perrone; A. Russo; M. Caldarulo; M. A. Russo