Literature DB >> 6687671

Hypoplasia of the right ventricular myocardium with ventricular tachycardia.

S Bharati, A W Feld, R Bauernfeind, A A Kattus, M Lev.   

Abstract

A 20-year-old woman died suddenly after having had recurrent ventricular tachycardia for five years. An ECG showed two distinct varieties of ventricular tachycardia, both characterized by left bundle-branch block. Pathologic examination showed what we considered to be a type of Uhl's anomaly. Most of the compact layer of the right ventricle was replaced by fat, with the trabeculated areas intact but showing severe fibrosis and chronic inflammation. Patches of such degeneration were also found in the septum and the left ventricle. The conduction system disclosed a septated bundle of His.

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Year:  1983        PMID: 6687671

Source DB:  PubMed          Journal:  Arch Pathol Lab Med        ISSN: 0003-9985            Impact factor:   5.534


  4 in total

1.  Familial right ventricular dysplasia with biventricular involvement and inflammatory infiltration. Heart Muscle Disease Study Group.

Authors:  B Pinamonti; D Miani; G Sinagra; R Bussani; F Silvestri; F Camerini
Journal:  Heart       Date:  1996-07       Impact factor: 5.994

Review 2.  The arrhythmogenic right ventricle. Dysplasia versus cardiomyopathy.

Authors:  G Fontaine; F Fontaliran; F R Andrade; E Velasquez; J Tonet; X Jouven; Y Fujioka; R Frank
Journal:  Heart Vessels       Date:  1995       Impact factor: 2.037

3.  Arrhythmogenic right ventricular dysplasia.

Authors:  G Fòntaine
Journal:  Br Heart J       Date:  1993-09

4.  Cardiac arrest in an adolescent with Uhl's anomaly: Two unusual cardiac arrhythmia mechanisms.

Authors:  Jeffrey P Moak; Gail D Pearson; Bradley Clark; Charles I Berul; Russell R Cross; Dilip S Nath
Journal:  HeartRhythm Case Rep       Date:  2016-05-26
  4 in total

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