Skip to Main Content
ADVERTISEMENT
SCROLL TO CONTINUE WITH CONTENT



Property Value
Status
Version
Ad File
Disable Ads Flag
Environment
Moat Init
Moat Ready
Contextual Ready
Contextual URL
Contextual Initial Segments
Contextual Used Segments
AdUnit
SubAdUnit
Custom Targeting
Ad Events
Invalid Ad Sizes
Advertisement
Heart Rhythm Case Reports
Close
  • Home
  • Articles and Issues
    • Back
    • Articles in Press
    • Current Issue
    • List of Issues
  • A Case for Education Quiz
    • Back
    • Current Quiz
    • Quiz Archive
  • For Authors
    • Back
    • About Open Access 
    • Author Information
    • Permissions
    • Researcher Academy 
    • Submit a Manuscript 
  • Journal Info
    • Back
    • About Open Access 
    • Contact Information
    • Editorial Board
    • Information for Advertisers
  • Society Info
    • Back
    • Heart Rhythm Society 
  • Heart Rhythm Society Journals
    • Back
    • Heart Rhythm
    • Heart Rhythm O2 
    • Cardiovascular Digital Health Journal 
  • HRCR Rare Diseases Article Collection 
  • Submit Your Manuscript 
Advanced searchSave search

Please enter a term before submitting your search.

Ok
  • Log in
  • Register
  • Log in
Skip menu
    x

    Filter:

    Filters applied

    • HRCR Rare Diseases Article Collection
    • September 2022 - March 2023Remove September 2022 - March 2023 filter
    Clear all

    Article Type

    • Case Reports17
    • Letter1

    Author

    • Anwer, Shehab1
    • Assaf, Nada1
    • Auf der Maur, Christoph1
    • Bahu, Marwan1
    • Bai, Rong1
    • Belhassen, Bernard1
    • Breitenstein, Alexander1
    • Bulbul, Ziad1
    • Bulj, Nikola1
    • Callans, David J1
    • Calvert, Peter1
    • Car, Siniša1
    • Cecchini, Federico1
    • Cerantola, Maxime1
    • Chaloupecký, Václav Jr1
    • Chandhok, Sheetal1
    • Charafeddine, Fatme1
    • Choudhury, Moinuddin1
    • Cunha Pachon, Carlos Thiene1
    • Davis, Megan1
    • Fabiano, Gennaro1
    • Flautt, Thomas1
    • Frankel, David S1
    • Fujiu, Katsuhito1
    • Gebauer, Roman1

    Journal

    • HeartRhythm Case Reports18

    Keyword

    • Atrial fibrillation3
    • Ventricular tachycardia3
    • Catheter ablation2
    • Congenital heart disease2
    • Ethanol ablation2
    • Sudden cardiac death2
    • Ablation1
    • Accessory pathway ablation1
    • Activation map1
    • Acute limb ischemia1
    • Anomalous coronary artery1
    • Arterial thromboembolism1
    • Asplenia syndrome1
    • Atrial tachycardia1
    • Atrioventricular nodal reentrant tachycardia1
    • Atrioventricular reciprocating tachycardia1
    • Autoimmune disease1
    • Balloon angioplasty1
    • Brugada syndrome1
    • Cardiac pacemaker1
    • Cardiac resynchronization1
    • Cardioneuroablation1
    • Carotid sinus syndrome1
    • Chagas disease1
    • CPVT1

    Access Filter

    • Open Access

    HRCR Rare Diseases Article Collection

    Read case reports pertaining to rare diseases

     

     

    Read case reports pertaining to rare diseases

    18 Results
    Subscribe to collection
    • Export
      • PDF
      • Citation

    Please select at least one article in order to proceed.

    Ok
    FilterHide Filter
    • Case Reports
      Open Access

      Demonstration of presence of a sling between anterior and posterior bundle branch during tachycardia using twin atrioventricular nodes: A case of asplenia syndrome

      HeartRhythm Case Reports
      In Press Corrected Proof
      Published online: January 30, 2023
      • Takahiko Kinjo
      • Masaomi Kimura
      • Taihei Itoh
      • Yuji Ishida
      • Hirofumi Tomita
      Cited in Scopus: 0
      • Preview Hide Preview
      • Download PDF
      • Export Citation
        Atrioventricular (AV) reciprocating tachycardia via twin AV nodes and corresponding AV bundles with a connecting sling has been reported in patients with asplenia and right isomerism.1,2 Although the presence of the sling has been reported histologically,3 its connection form and electrophysiological properties remain to be elucidated.
        Demonstration of presence of a sling between anterior and posterior bundle branch during tachycardia using twin atrioventricular nodes: A case of asplenia syndrome
      • Case Reports
        Open Access

        Very delayed pericarditis associated with ethanol ablation of the vein of Marshall for treatment of atrial fibrillation

        HeartRhythm Case Reports
        In Press Corrected Proof
        Published online: January 28, 2023
        • Koichiro Motoki
        • Takaomi Harada
        • Shinobu Hosokawa
        • Tomoko Hara
        • Kiyoshige Yamamoto
        • Koichi Kishi
        Cited in Scopus: 0
        • Preview Hide Preview
        • Download PDF
        • Export Citation
          Catheter ablation of persistent atrial fibrillation has limited success. Procedural strategies beyond pulmonary vein isolation have failed to consistently improve results.
          Very delayed pericarditis associated with ethanol ablation of the vein of Marshall for treatment of atrial fibrillation
        • Case Reports
          Open Access

          Multiple recurrent episodes of pacemaker-associated postcardiac injury syndrome

          HeartRhythm Case Reports
          In Press Corrected Proof
          Published online: January 24, 2023
          • Eriko Hasumi
          • Katsuhito Fujiu
          • Issei Komuro
          Cited in Scopus: 0
          • Preview Hide Preview
          • Download PDF
          • Export Citation
            Postcardiac injury syndrome (PCIS) is an autoimmune disease that causes damage to the pericardium, myocardium, and pleura after myocardial infarction, cardiac surgery, or trauma. Although most cases are benign, anti-inflammatory agents may be used to treat PCIS. Rarely, PCIS may become refractory or recur after anti-inflammatory treatment.1 In such cases, long-term oral corticosteroids are usually prescribed2; however, the optimal duration of administration remains unclear. We report a patient who experienced multiple recurrent episodes of pacemaker lead–related PCIS that were treated with oral prednisone and pericardial drainage.
            Multiple recurrent episodes of pacemaker-associated postcardiac injury syndrome
          • Case Reports
            Open Access

            Idiopathic premature ventricular contraction–triggered ventricular fibrillation: Subcutaneous implantable cardioverter-defibrillator (S-ICD) template matched ablation in the absence of inducible clinical premature ventricular contraction

            HeartRhythm Case Reports
            In Press Corrected Proof
            Published online: January 15, 2023
            • Sudeepthi Reddy Mekala
            • Megan Davis
            • Komandoor Srivathsan
            Cited in Scopus: 0
            • Preview Hide Preview
            • Download PDF
            • Export Citation
              Idiopathic ventricular fibrillation is diagnosed in patients who have survived sudden cardiac arrest from ventricular fibrillation (VF) without identifiable structural heart disease.1 It is the main cause of unexplained sudden cardiac death, particularly in young patients under the age of 35.2 An implantable cardioverter-defibrillator (ICD) is usually recommended for the secondary prevention of sudden cardiac death. VF ablation is recommended for clinical VF recurrence and for reducing the number of ICD shocks.
              Idiopathic premature ventricular contraction–triggered ventricular fibrillation: Subcutaneous implantable cardioverter-defibrillator (S-ICD) template matched ablation in the absence of inducible clinical premature ventricular contraction
            • Case Reports
              Open Access

              An unexpected finding by epicardial mapping: Atrial fibrillation in a 14-month-old patient with short QT syndrome

              HeartRhythm Case Reports
              In Press Corrected Proof
              Published online: December 31, 2022
              • Mathijs S. van Schie
              • Nawin L. Ramdat Misier
              • Wouter J. van Leeuwen
              • Yannick J.H.J. Taverne
              • Natasja M.S. de Groot
              Cited in Scopus: 0
              • Preview Hide Preview
              • Download PDF
              • Export Citation
                Short QT syndrome (SQTS) is a very rare channelopathy accompanied by familial clustering and sudden cardiac death.1 It has an estimated prevalence ranging from 0.02% up to 2% in the adult population, but only 0.05% among pediatric patients.2–6 To date, 9 mutations in 6 different genes have been identified, including KCNH2, KCNQ1, KCNJ1, CACNA1C, CACNB2, and CACNA2D1. In pediatric patients, SQTS is characterized by shortening of the corrected QT interval (QTcB <316 ms, J-Tpeak cB <181 ms, and the presence of early repolarization) on the surface electrocardiogram (ECG).
                An unexpected finding by epicardial mapping: Atrial fibrillation in a 14-month-old patient with short QT syndrome
              • Case Reports
                Open Access

                Right ventricular outflow tract ablation close to an anomalous right coronary artery: When imaging meets electrophysiology

                HeartRhythm Case Reports
                In Press Corrected Proof
                Published online: December 28, 2022
                • Peter Calvert
                • Moinuddin Choudhury
                • Afshin Khalatbari
                • Richard Snowdon
                • Dhiraj Gupta
                • Simon Modi
                • and others
                Cited in Scopus: 0
                • Preview Hide Preview
                • Download PDF
                • Export Citation
                • Video
                Catheter ablation is a commonly undertaken and highly effective treatment for symptomatic right ventricular outflow tract (RVOT) ventricular ectopy / ventricular tachycardia (VT).1 Despite the high chance of cure with ablation, caution is required to avoid collateral injury to coronary arteries in certain well-described locations. Anomalous coronary arteries are rare2 and may have an unfamiliar path involving the outflow tracts, posing a significantly increased risk with ablation. The approach to outflow tract ablation in a patient with an anomalous coronary artery has not been previously reported.
                Right ventricular outflow tract ablation close to an anomalous right coronary artery: When imaging meets electrophysiology
              • Case Report
                Open Access

                Novel trans-2,3-enoyl-CoA reductase–like variant associated with catecholaminergic polymorphic ventricular tachycardia type 3

                HeartRhythm Case Reports
                Vol. 9Issue 3p171–177Published online: December 20, 2022
                • Fatme Charafeddine
                • Nada Assaf
                • Ali Ismail
                • Ziad Bulbul
                Cited in Scopus: 0
                • Preview Hide Preview
                • Download PDF
                • Export Citation
                  Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited arrhythmia syndrome characterized by polymorphic ventricular tachycardia, usually provoked by emotional stress or exercise, in the absence of any structural cardiac abnormality, and in the presence of often normal resting electrocardiogram (ECG).1 It is a highly lethal disease with an overall mortality of 30%–40% if left untreated.2 Studies have shown that almost 35% of affected individuals become symptomatic before the age of 10 and 75% before the age of 20 years.
                  Novel trans-2,3-enoyl-CoA reductase–like variant associated with catecholaminergic polymorphic ventricular tachycardia type 3
                • Case Report
                  Open Access

                  Left bundle branch area pacing for the treatment of painful left bundle branch block syndrome

                  HeartRhythm Case Reports
                  Vol. 9Issue 2p121–125Published online: December 9, 2022
                  • Maxime Cerantola
                  • David S. Frankel
                  • David J. Callans
                  • Pasquale Santangeli
                  • Robert D. Schaller
                  Cited in Scopus: 0
                  • Preview Hide Preview
                  • Download PDF
                  • Export Citation
                    Painful left bundle branch block (LBBB) syndrome causes intermittent or chronic chest pain and/or shortness of breath in the absence of myocardial ischemia.1 Given its low prevalence and association with coronary artery disease, it is frequently not recognized, making its true prevalence unknown. The mechanistic nature of the associated chest pain has not been completely elucidated but is thought to be related to ventricular dyssynchrony2 and interoceptive hypersensitivity.3 Treatment options include the use of beta-blockers to reduce heart rate and cardiac pacing therapy aimed at reestablishing normal ventricular activation, through biventricular or His bundle pacing (HBP).
                    Left bundle branch area pacing for the treatment of painful left bundle branch block syndrome
                  • Case Report
                    Open Access

                    Groin lymphorrhea after catheter ablation of atrial fibrillation: A case report

                    HeartRhythm Case Reports
                    Vol. 9Issue 3p178–180Published online: December 9, 2022
                    • Mihovil Santini
                    • Kristijan Đula
                    • Vjekoslav Radeljić
                    • Siniša Car
                    • Nikola Bulj
                    • Ivan Zeljković
                    Cited in Scopus: 0
                    • Preview Hide Preview
                    • Download PDF
                    • Export Citation
                      Catheter ablation is a well-established therapeutic option for the treatment of atrial fibrillation (AF).1,2 Although nowadays performed on a routine basis, catheter ablation of atrial fibrillation (AFCA) is associated with a non-negligible complication rate of up to 16% with significant discrepancies in incidence and type, with vascular access site complications being the most common (groin hematoma, femoral arterial pseudoaneurysms, and femoral arteriovenous fistula).1–4 We report a case of a 75-year-old White male patient with right groin lymphorrhea as an access site–related complication after second catheter ablation of recurrent atrial fibrillation.
                      Groin lymphorrhea after catheter ablation of atrial fibrillation: A case report
                    • Case Report
                      Open Access

                      A case of successful catheter ablation for biatrial reentrant tachycardia after a Mustard operation for dextro-transposition of the great arteries

                      HeartRhythm Case Reports
                      Vol. 9Issue 3p140–143Published online: December 5, 2022
                      • Yuka Taguchi
                      • Katsumi Matsumoto
                      • Morio Shoda
                      • Manabu Nitta
                      • Junya Hosoda
                      • Toshiyuki Ishikawa
                      Cited in Scopus: 0
                      • Preview Hide Preview
                      • Download PDF
                      • Export Citation
                        Mustard and Senning operations are atrial switch techniques for dextro-transposition of the great arteries (d-TGA) that have been mainly performed during a period from the 1960s to the mid-1980s.
                        A case of successful catheter ablation for biatrial reentrant tachycardia after a Mustard operation for dextro-transposition of the great arteries
                      • Case Report
                        Open Access

                        Incessant atrioventricular nodal reentrant tachycardia resulting in tachycardia-induced cardiomyopathy and catastrophic embolization of left ventricular thrombus

                        HeartRhythm Case Reports
                        Vol. 9Issue 3p144–147Published online: December 5, 2022
                        • Roy Taoutel
                        • Fares Sukhon
                        • Steven Liskov
                        • Bahij Kreidieh
                        • Sheetal Chandhok
                        Cited in Scopus: 0
                        • Preview Hide Preview
                        • Download PDF
                        • Export Citation
                          Atrioventricular nodal reentrant tachycardia (AVNRT) is a common paroxysmal supraventricular tachycardia (SVT) featuring repetitive salvos with spontaneous termination. Few reports exist demonstrating incessant AVNRT with chronically uncontrolled ventricular rates and tachycardia-induced cardiomyopathy (TIC).1,2 Persistent cases of incessant AVNRT resulting in TIC and intracavitary thrombus are exceedingly rare.2 We report a case of incessant slow/fast AVNRT associated with TIC and catastrophic embolization of left ventricular (LV) thrombus treated with acute radiofrequency slow pathway modification.
                          Incessant atrioventricular nodal reentrant tachycardia resulting in tachycardia-induced cardiomyopathy and catastrophic embolization of left ventricular thrombus
                        • Case Report
                          Open Access

                          Successful ablation of ventricular tachycardia in a patient with Chagas disease using ethanol ablation in the coronary venous system: A case report

                          HeartRhythm Case Reports
                          Vol. 9Issue 2p109–112Published online: December 3, 2022
                          • Thomas Flautt
                          • Miguel Valderrábano
                          Cited in Scopus: 0
                          • Preview Hide Preview
                          • Download PDF
                          • Export Citation
                            Chagas disease is a parasitic zoonosis that constitutes a severe public health problem and is endemic in 21 Latin American countries.1 It is estimated that between 6 and 8 million people are infected with Trypanosoma cruzi (T cruzi), with an additional 65 million at risk of acquiring the disease by vector-borne transmission, blood or congenital transmission, or food-borne transmission.2,3 Chagas disease has an acute, indeterminate, and chronic phase. If untreated, the acute phase may transition to an indeterminate phase characterized by seropositivity for T cruzi in the absence of clinical symptoms.
                            Successful ablation of ventricular tachycardia in a patient with Chagas disease using ethanol ablation in the coronary venous system: A case report
                          • Case Report
                            Open Access

                            Carotid sinus syndrome treated by cardioneuroablation: Is sinus node denervation enough? Insights from a syncope recurrence report

                            HeartRhythm Case Reports
                            Vol. 9Issue 1p48–52Published online: October 31, 2022
                            • Juan Carlos Zerpa Acosta
                            • Kleber Oliveira de Souza
                            • Felipe Augusto Ortencio
                            • Carlos Thiene Cunha Pachon
                            • Enrique Indalecio Pachon Mateos
                            • Jose Carlos Pachon Mateos
                            Cited in Scopus: 1
                            • Preview Hide Preview
                            • Download PDF
                            • Export Citation
                              Cardioneuroablation (CNA) has been proposed as an alternative treatment for patients with refractory vasovagal syncope (VVS), functional atrioventricular block (AVB), or functional bradyarrhythmia instead of classical treatment or pacemaker.1 Vagal denervation is achieved by endocardial catheter ablation targeting atrial fibrillation nests (AFN)2 and ganglionic plexus (GP)-related areas. We describe a clinical case of cardioinhibitory carotid sinus syndrome (CSS) treated with CNA, where partial vagal denervation was achieved over sinus node.
                              Carotid sinus syndrome treated by cardioneuroablation: Is sinus node denervation enough? Insights from a syncope recurrence report
                            • Letter to the Editor
                              Open Access

                              To the Editor—Concealed His or Purkinje extrasystoles?

                              HeartRhythm Case Reports
                              Vol. 8Issue 12p863Published online: October 21, 2022
                              • Bernard Belhassen
                              Cited in Scopus: 0
                              • Preview Hide Preview
                              • Download PDF
                              • Export Citation
                                I read with interest the case report by Ho and colleagues.1 I would like to present arguments suggesting alternative diagnoses.
                              • Case Report
                                Open Access

                                Improved symptoms, exercise capacity, and homogeneity of cardiac deformation through conduction system pacing in a patient with symptomatic left bundle branch block

                                HeartRhythm Case Reports
                                Vol. 9Issue 1p43–47Published online: October 18, 2022
                                • Daniel Hofer
                                • Shehab Anwer
                                • Felix C. Tanner
                                • Christoph Auf der Maur
                                • Jan Steffel
                                • Sergio Richter
                                • and others
                                Cited in Scopus: 0
                                • Preview Hide Preview
                                • Download PDF
                                • Export Citation
                                • Video
                                Painful left bundle branch syndrome is a clinical entity consisting of exertional angina and rate-dependent left bundle branch block (LBBB), affecting patients of all age and sex.1 Because of potentially coexisting other cardiac diseases (ie, cardiomyopathy, coronary artery disease) that may mimic both LBBB and symptoms, the true prevalence is unknown, but fewer than 60 cases have been reported so far.1 Diagnostic criteria do not officially exist, but simultaneous onset of LBBB and angina during exercise test support the diagnosis.
                                Improved symptoms, exercise capacity, and homogeneity of cardiac deformation through conduction system pacing in a patient with symptomatic left bundle branch block
                              • Case Report
                                Open Access

                                Electrophysiology and surgery intertwined in complex treatment of Ebstein’s anomaly in childhood

                                HeartRhythm Case Reports
                                Vol. 9Issue 1p17–22Published online: September 30, 2022
                                • Václav Chaloupecký Jr.
                                • Roman Gebauer
                                • Jan Kovanda
                                • Karel Koubský
                                • Ioana Sus
                                • Jan Janoušek
                                Cited in Scopus: 0
                                • Preview Hide Preview
                                • Download PDF
                                • Export Citation
                                • Video
                                Ebstein’s anomaly, a rare and highly variable congenital heart defect,1 still presents a treatment challenge. The currently used cone repair of the tricuspid valve has carried favorable results in suitable patients.2 Arrhythmogenic substrates including accessory pathways3,4 and right bundle branch block5 associated with electromechanical ventricular dyssynchrony present additional therapeutic targets. We present a patient with Ebstein’s anomaly of tricuspid valve and Wolff-Parkinson-White syndrome in whom joint electrophysiological and surgical interventions were used to address all major disease components.
                                Electrophysiology and surgery intertwined in complex treatment of Ebstein’s anomaly in childhood
                              • Case Report
                                Open Access

                                Epicardial multisite conduction blocks detected by equispaced electrode array and omnipolar technology in Brugada syndrome

                                HeartRhythm Case Reports
                                Vol. 9Issue 1p12–16Published online: September 30, 2022
                                • Saverio Iacopino
                                • Federico Cecchini
                                • Alberto Tripodi
                                • Paolo Sorrenti
                                • Gennaro Fabiano
                                • Andrea Petretta
                                Cited in Scopus: 0
                                • Preview Hide Preview
                                • Download PDF
                                • Export Citation
                                • Video
                                Brugada syndrome (BrS) is an inherited channelopathy linked to an increased risk of developing malignant ventricular arrhythmias and sudden cardiac death in otherwise healthy individuals.1 Currently, implantable cardioverter-defibrillator (ICD) is still the mainstay of treatment for BrS,1 but for patients experiencing recurrent ICD shocks despite optimal medical therapy, radiofrequency (RF) transcatheter ablation of the arrhythmogenic substrate is an available option with promising results.2–5 Although there is a generalized consensus in considering the right ventricular outflow tract (RVOT) epicardium as the locus harboring the pathologic substrate, the exact pathogenesis of BrS is still a matter of debate.
                                Epicardial multisite conduction blocks detected by equispaced electrode array and omnipolar technology in Brugada syndrome
                              • Case Report
                                Open Access

                                Localized intramural reentry confined within the ventricular septum in lamin cardiomyopathy

                                HeartRhythm Case Reports
                                Vol. 8Issue 12p840–844Published online: September 22, 2022
                                • Jake Martinez
                                • Rong Bai
                                • Marwan Bahu
                                • Michael F. Morris
                                • J. Peter Weiss
                                • Roderick Tung
                                Cited in Scopus: 0
                                • Preview Hide Preview
                                • Download PDF
                                • Export Citation
                                  High-resolution electroanatomic mapping systems have greatly improved the ability to characterize the size and dimensions of the reentrant circuit responsible for human ventricular tachycardia (VT). The minimal dimension of critical isthmus regions may be less than 1 cm in more than 25% of circuits mapped.1 Despite advanced, detailed simultaneous epicardial and endocardial mapping, detection of intramural circuit components remains challenging. Epicardial mapping through coronary venous branches has gained popularity owing to refinement of mapping catheters and novel use of transcoronary venous ethanol.
                                  Localized intramural reentry confined within the ventricular septum in lamin cardiomyopathy
                                Page 1 of 1

                                Login to your account

                                Show
                                Forgot password?
                                Don’t have an account?
                                Create a Free Account

                                If you don't remember your password, you can reset it by entering your email address and clicking the Reset Password button. You will then receive an email that contains a secure link for resetting your password

                                If the address matches a valid account an email will be sent to __email__ with instructions for resetting your password

                                Cancel
                                • Home
                                • Articles and Issues
                                • Articles in Press
                                • Current Issue
                                • List of Issues
                                • HRCR Rare Diseases Article Collection
                                • A Case for Education Quiz
                                • Current Quiz
                                • Quiz Archive
                                • For Authors
                                • About Open Access
                                • Author Information
                                • Permissions
                                • Researcher Academy
                                • Submit a Manuscript
                                • Journal Info
                                • About Open Access
                                • Info for Advertisers
                                • Contact Information
                                • Editorial Board
                                • Society Info
                                • Heart Rhythm Society
                                • Heart Rhythm Society Journals
                                • Heart Rhythm
                                • Heart Rhythm O2
                                • Cardiovascular Digital Health Journal
                                • Follow Us
                                • Facebook
                                • Twitter
                                • RSS Feed

                                The content on this site is intended for healthcare professionals.



                                We use cookies to help provide and enhance our service and tailor content. To update your cookie settings, please visit the Cookie Preference Center for this site.
                                Copyright © 2023 Elsevier Inc. except certain content provided by third parties.

                                • Privacy Policy  
                                • Terms and Conditions  
                                • Accessibility  
                                • Help & Contact

                                RELX