المؤلفون: Nomura A; Department of Emergency and Critical Care Medicine, Dokkyo Medical University, Japan.; Department of Cardiovascular Medicine and Nephrology, Dokkyo Medical University Nikko Medical Center, Japan., Otani N; Department of Cardiology, Dokkyo Medical University Nikko Medical Center, Japan., Kokubun A; Department of Cardiovascular Medicine and Nephrology, Dokkyo Medical University Nikko Medical Center, Japan.; Department of Diagnostic and Generalist Medicine, Dokkyo Medical University, Japan., Mizuguchi S; Department of Cardiovascular Medicine and Nephrology, Dokkyo Medical University Nikko Medical Center, Japan., Kawamoto S; Department of Cardiovascular Medicine and Nephrology, Dokkyo Medical University Nikko Medical Center, Japan.; Department of Diagnostic and Generalist Medicine, Dokkyo Medical University, Japan., Tomoe T; Department of Cardiovascular Medicine and Nephrology, Dokkyo Medical University Nikko Medical Center, Japan., Kitahara K; Department of Cardiovascular Medicine and Nephrology, Dokkyo Medical University Nikko Medical Center, Japan., Sugiyama T; Department of Cardiovascular Medicine and Nephrology, Dokkyo Medical University Nikko Medical Center, Japan., Horie Y; Department of Cardiology, Dokkyo Medical University Nikko Medical Center, Japan., Sugimura H; Department of Cardiology, Dokkyo Medical University Nikko Medical Center, Japan., Yasu T; Department of Cardiovascular Medicine and Nephrology, Dokkyo Medical University Nikko Medical Center, Japan.

المصدر: Internal medicine (Tokyo, Japan) [Intern Med] 2024 Jun 15; Vol. 63 (12), pp. 1739-1743. Date of Electronic Publication: 2023 Nov 13.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Japanese Society of Internal Medicine Country of Publication: Japan NLM ID: 9204241 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1349-7235 (Electronic) Linking ISSN: 09182918 NLM ISO Abbreviation: Intern Med Subsets: MEDLINE

مواضيع طبية MeSH: Dextrocardia*/diagnostic imaging , Dextrocardia*/complications , Situs Inversus*/diagnostic imaging , Situs Inversus*/complications , Pacemaker, Artificial* , Imaging, Three-Dimensional* , Tomography, X-Ray Computed*, Humans ; Female ; Aged ; Sick Sinus Syndrome/therapy ; Sick Sinus Syndrome/diagnostic imaging ; Sick Sinus Syndrome/complications ; Prosthesis Implantation/methods ; Prosthesis Implantation/instrumentation ; Treatment Outcome

مستخلص: We herein report a 76-year-old woman with situs inversus and dextrocardia who underwent pacemaker implantation for sick sinus syndrome. Situs inversus with dextrocardia, which is frequently associated with cardiovascular malformation, is a rare congenital malformation wherein the thoracic and abdominal viscera are inverted compared with their normal positions. This renders the implantation of cardiac devices an arduous task. We therefore decided to gather preoperative anatomical information on patients with situs inversus and dextrocardia. We used three-dimensional computed tomography to collect preoperative information in order to facilitate the safe implantation of cardiac devices.

المؤلفون: Tien DA; University of Medicine and Pharmacy, Vietnam National University, Hanoi, Vietnam.; CardioVascular Center-E Hospital, Hanoi, Vietnam., Bao LT; CardioVascular Center-E Hospital, Hanoi, Vietnam., Phuong DH; CardioVascular Center-E Hospital, Hanoi, Vietnam., Nhu Huyen LT; CardioVascular Center-E Hospital, Hanoi, Vietnam., Thuy NT; University of Medicine and Pharmacy, Vietnam National University, Hanoi, Vietnam.; CardioVascular Center-E Hospital, Hanoi, Vietnam.

المصدر: Asian cardiovascular & thoracic annals [Asian Cardiovasc Thorac Ann] 2024 May; Vol. 32 (4), pp. 231-233. Date of Electronic Publication: 2024 May 20.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Sage Country of Publication: England NLM ID: 9503417 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1816-5370 (Electronic) Linking ISSN: 02184923 NLM ISO Abbreviation: Asian Cardiovasc Thorac Ann Subsets: MEDLINE

مواضيع طبية MeSH: Situs Inversus*/complications , Situs Inversus*/diagnostic imaging , Situs Inversus*/surgery , Dextrocardia*/complications , Dextrocardia*/diagnostic imaging , Dextrocardia*/surgery , Tetralogy of Fallot*/surgery , Tetralogy of Fallot*/diagnostic imaging , Tetralogy of Fallot*/complications , Thoracotomy* , Coronary Vessel Anomalies*/surgery , Coronary Vessel Anomalies*/complications , Coronary Vessel Anomalies*/diagnostic imaging , Abnormalities, Multiple*/surgery, Humans ; Treatment Outcome ; Male ; Cardiac Surgical Procedures

مستخلص: We present a rare case of tetralogy of Fallot accompanied with dextrocardia, situs inversus and anomalous origin of the right coronary artery. Total repair was accomplished successfully using a minimally invasive left axillary thoracotomy.
Competing Interests: Declaration of conflicting interestsThe author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

عنوان ترانسليتريتد: Situs Inversuslu ve Dekstrokardili Bir Hastada Atriyal Fibrilasyonun Kriyobalon ile Ablasyonu.

المؤلفون: Çay S; Division of Arrhythmia and Electrophysiology, Department of Cardiology, University of Health Sciences, Yuksek Ihtisas Cardiovascular Building, Ankara City Hospital, Ankara, Türkiye., Özeke Ö; Division of Arrhythmia and Electrophysiology, Department of Cardiology, University of Health Sciences, Yuksek Ihtisas Cardiovascular Building, Ankara City Hospital, Ankara, Türkiye., Özcan F; Division of Arrhythmia and Electrophysiology, Department of Cardiology, University of Health Sciences, Yuksek Ihtisas Cardiovascular Building, Ankara City Hospital, Ankara, Türkiye., Kara M; Division of Arrhythmia and Electrophysiology, Department of Cardiology, University of Health Sciences, Yuksek Ihtisas Cardiovascular Building, Ankara City Hospital, Ankara, Türkiye., Özcan Çetin EH; Division of Arrhythmia and Electrophysiology, Department of Cardiology, University of Health Sciences, Yuksek Ihtisas Cardiovascular Building, Ankara City Hospital, Ankara, Türkiye., Korkmaz A; Division of Arrhythmia and Electrophysiology, Department of Cardiology, University of Health Sciences, Yuksek Ihtisas Cardiovascular Building, Ankara City Hospital, Ankara, Türkiye., Topaloğlu S; Division of Arrhythmia and Electrophysiology, Department of Cardiology, University of Health Sciences, Yuksek Ihtisas Cardiovascular Building, Ankara City Hospital, Ankara, Türkiye.

المصدر: Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir [Turk Kardiyol Dern Ars] 2024 Jun; Vol. 52 (4), pp. 300-301.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Kare Country of Publication: Turkey NLM ID: 9426239 Publication Model: Print Cited Medium: Internet ISSN: 1308-4488 (Electronic) Linking ISSN: 10165169 NLM ISO Abbreviation: Turk Kardiyol Dern Ars Subsets: MEDLINE

مواضيع طبية MeSH: Atrial Fibrillation*/surgery , Atrial Fibrillation*/complications , Dextrocardia*/diagnostic imaging , Dextrocardia*/complications , Dextrocardia*/surgery , Situs Inversus*/complications , Situs Inversus*/diagnostic imaging , Cryosurgery*/methods, Humans ; Male ; Middle Aged

المؤلفون: Shahani R; Northwell Health, New Hyde Park, New York.; Northwell Health, Staten Island University Hospital Heart Institute, Staten Island, New York.; Department of Cardiothoracic Surgery, Staten Island University Hospital Heart Institute, Staten Island, New York., Ahmed A; Northwell Health, New Hyde Park, New York.; City University of New York School of Medicine, New York, New York., Rosell FM; Northwell Health, New Hyde Park, New York.; Northwell Health, Staten Island University Hospital Heart Institute, Staten Island, New York.; Department of Cardiothoracic Surgery, Staten Island University Hospital Heart Institute, Staten Island, New York., Iribarne A; Northwell Health, New Hyde Park, New York.; Northwell Health, Staten Island University Hospital Heart Institute, Staten Island, New York.; Department of Cardiothoracic Surgery, Staten Island University Hospital Heart Institute, Staten Island, New York.

المصدر: Texas Heart Institute journal [Tex Heart Inst J] 2024 Apr 16; Vol. 51 (1).

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: published in the Cardiovascular Surgical Research Laboratories, Texas Heart Institute Country of Publication: United States NLM ID: 8214622 Publication Model: Print Cited Medium: Internet ISSN: 1526-6702 (Electronic) Linking ISSN: 07302347 NLM ISO Abbreviation: Tex Heart Inst J Subsets: MEDLINE

مواضيع طبية MeSH: Coronary Artery Disease*/complications , Coronary Artery Disease*/diagnosis , Coronary Artery Disease*/surgery , Situs Inversus*/complications , Situs Inversus*/diagnosis , Situs Inversus*/surgery , Dextrocardia*/complications , Dextrocardia*/surgery, Male ; Humans ; Middle Aged ; Coronary Artery Bypass ; Rare Diseases

مستخلص: Dextrocardia with situs inversus totalis is a rare hereditary condition characterized by reversed orientation of the major thoracic and abdominal organs. Though dextrocardia itself is not believed to increase the risk of coronary artery disease, the workup and surgical management of patients with this condition may be technically challenging to heart team clinicians. This report describes the case management of a high-risk 56-year-old man with dextrocardia who presented with multivessel coronary artery disease.
(© 2024 The Authors. Published by The Texas Heart Institute®.)

المؤلفون: Karmegaraj B; Sowmi Pediatric Heart Centre, Swasthik Fetal Heart Unit, Tirunelveli, Tamil Nadu, India.; Fetal Cardiology Division, Department of Paediatric Cardiology, Amrita Institute of Medical Sciences and Research Centre, Kochi, Kerala, India.

المصدر: Echocardiography (Mount Kisco, N.Y.) [Echocardiography] 2024 Feb; Vol. 41 (2), pp. e15788.

نوع المنشور: Case Reports

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 8511187 Publication Model: Print Cited Medium: Internet ISSN: 1540-8175 (Electronic) Linking ISSN: 07422822 NLM ISO Abbreviation: Echocardiography Subsets: MEDLINE

مواضيع طبية MeSH: Dextrocardia*/complications , Dextrocardia*/diagnostic imaging , Heart Defects, Congenital* , Heart Septal Defects, Ventricular*, Humans ; Aorta/abnormalities ; Fetus

مستخلص: Three-dimensional virtual dissection using high-definition live tissue rendering ultrasound tool of a 23-week gestation fetus with situs solitus, mirror image dextrocardia, ventricular septal defect, aortic override, and pulmonary atresia.
(© 2024 Wiley Periodicals LLC.)

المؤلفون: Guo Z; Orthopedics Department of the Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, China., Li D; Orthopedics Department of the Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, China., Zang X; Department of Orthopaedics, Qilu Hospital of Shandong University, Jinan, People's Republic of China.

المصدر: Medicine [Medicine (Baltimore)] 2024 Mar 29; Vol. 103 (13), pp. e37625.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 2985248R Publication Model: Print Cited Medium: Internet ISSN: 1536-5964 (Electronic) Linking ISSN: 00257974 NLM ISO Abbreviation: Medicine (Baltimore) Subsets: MEDLINE

مواضيع طبية MeSH: Dextrocardia*/complications , Dextrocardia*/diagnostic imaging , Dextrocardia*/surgery , Situs Inversus*/complications , Situs Inversus*/diagnostic imaging , Musculoskeletal Abnormalities*/surgery, Female ; Humans ; Child, Preschool ; Laminectomy ; Treatment Outcome

مستخلص: Rationale: Situs inversus totalis is a rare malposition of organs that typically involves lesions in the respiratory, circulatory, or urinary systems. Cases of congenital hemivertebrae combined with situs inversus totalis are extremely rare and have limited reports.
Patient Concerns: We report a 2.5 years old girl with 2 congenital hemipyramids and complete visceral inversion who ultimately underwent hemilaminectomy.
Diagnosis: Congenital hemivertebrae combined with situs inversus totalis.
Intervention: The patient underwent hemilaminectomy.
Outcomes: The spinal deformity was corrected.
Lessons: For patient with spinal deformities combined with situs inversus totalis, surgery can be an effective treatment method. But we also need to be vigilant about the dysfunction of various systems.
Competing Interests: The authors have no conflicts of interest to disclose.
(Copyright © 2024 the Author(s). Published by Wolters Kluwer Health, Inc.)

المؤلفون: Kelley BP; Division of Cardiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Glasco S; Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Sang CJ 3rd; Division of Cardiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Yoo B; Division of Cardiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Yeung M; Division of Cardiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA., Zhang J; Division of Cardiology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.

المصدر: Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions [Catheter Cardiovasc Interv] 2024 Mar; Vol. 103 (4), pp. 565-569. Date of Electronic Publication: 2024 Feb 12.

نوع المنشور: Case Reports

بيانات الدورية: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 100884139 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1522-726X (Electronic) Linking ISSN: 15221946 NLM ISO Abbreviation: Catheter Cardiovasc Interv Subsets: MEDLINE

مواضيع طبية MeSH: Dextrocardia* , Angioplasty, Balloon, Coronary* , Percutaneous Coronary Intervention*/adverse effects, Humans ; Treatment Outcome ; Coronary Angiography

مستخلص: Coronary angioplasty in patients with a right-sided heart may be difficult due to challenges in engaging the coronary arteries, interpreting angiogram, and further delivering intracoronary therapies. We present our experience of percutaneous coronary intervention in two cases and propose a practical algorithm to approach cardiac catheterization in these patients.
(© 2024 Wiley Periodicals LLC.)

المؤلفون: Wang Y; Department of Nephrology, Blood Purification Research Center, the First Affiliated Hospital, Fujian Medical University, Fuzhou, China.; Fujian Clinical Research Center for Metabolic Chronic Kidney Disease, the First Affiliated Hospital, Fujian Medical University, Fuzhou, China.; Department of Nephrology, National Regional Medical Center, Binhai Campus of the First Affiliated Hospital, Fujian Medical University, Fuzhou, China., Chen C; Department of Nephrology, Blood Purification Research Center, the First Affiliated Hospital, Fujian Medical University, Fuzhou, China.; Fujian Clinical Research Center for Metabolic Chronic Kidney Disease, the First Affiliated Hospital, Fujian Medical University, Fuzhou, China.; Department of Nephrology, National Regional Medical Center, Binhai Campus of the First Affiliated Hospital, Fujian Medical University, Fuzhou, China., Xu Y; Department of Nephrology, Blood Purification Research Center, the First Affiliated Hospital, Fujian Medical University, Fuzhou, China.; Fujian Clinical Research Center for Metabolic Chronic Kidney Disease, the First Affiliated Hospital, Fujian Medical University, Fuzhou, China.; Department of Nephrology, National Regional Medical Center, Binhai Campus of the First Affiliated Hospital, Fujian Medical University, Fuzhou, China.

المصدر: QJM : monthly journal of the Association of Physicians [QJM] 2024 Feb 26; Vol. 117 (2), pp. 140-141.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Published for the Association of Physicians of Great Britain and Ireland by the Oxford University Press Country of Publication: England NLM ID: 9438285 Publication Model: Print Cited Medium: Internet ISSN: 1460-2393 (Electronic) Linking ISSN: 14602393 NLM ISO Abbreviation: QJM Subsets: MEDLINE

مواضيع طبية MeSH: Truncus Arteriosus, Persistent* , Heart Defects, Congenital* , Dextrocardia*/complications , Dextrocardia*/diagnostic imaging, Adult ; Humans

SCR Disease Name: Conotruncal cardiac defects

المؤلفون: Kozyk M; Department of Internal Medicine, Corewell Health William Beaumont University Hospital, Royal Oak, MI, USA., Usenko OY; Department of Thoracoabdominal Surgery, O.O. Shalimov National Institute of Surgery and Transplantology, Kyiv, Ukraine., Kessler SA; Oakland University William Beaumont School of Medicine, Rochester, MI, USA., Shkarban VP; Department of Pancreatic Surgery, O.O. Shalimov National Institute of Surgery and Transplantology, Kyiv, Ukraine., Tereshkevych IS; Department of Endoscopy, O.O. Shalimov National Institute of Surgery and Transplantology, Kyiv, Ukraine., Babii IV; Department of Endoscopy, O.O. Shalimov National Institute of Surgery and Transplantology, Kyiv, Ukraine., Sanzharov OM; Department of Endoscopy, O.O. Shalimov National Institute of Surgery and Transplantology, Kyiv, Ukraine., Strubchevska K; Department of Internal Medicine, Corewell Health William Beaumont University Hospital, Royal Oak, MI, USA.

المصدر: The American journal of case reports [Am J Case Rep] 2024 Mar 07; Vol. 25, pp. e942006. Date of Electronic Publication: 2024 Mar 07.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: International Scientific Information, Inc Country of Publication: United States NLM ID: 101489566 Publication Model: Electronic Cited Medium: Internet ISSN: 1941-5923 (Electronic) Linking ISSN: 19415923 NLM ISO Abbreviation: Am J Case Rep Subsets: MEDLINE

مواضيع طبية MeSH: Dextrocardia*/complications , Pancreatic Pseudocyst*/diagnostic imaging , Pancreatic Pseudocyst*/surgery , Pancreatic Pseudocyst*/complications , Situs Inversus*/complications , Situs Inversus*/diagnosis, Female ; Humans ; Middle Aged ; Abdomen ; Tomography, X-Ray Computed

مستخلص: BACKGROUND Duplication of the gastrointestinal tract is a rare congenital malformation that can develop in any part of the digestive tract. These duplications may be asymptomatic into adult age. Situs inversus totalis is a rare congenital anomaly characterized by a mirror transposition of thoracic and abdominal organs. We present a case of a pancreatic pseudocyst in a patient with a combination of situs inversus totalis and doubling of the esophagus, stomach, and first part of the duodenum. CASE REPORT A 64-year-old woman presented with epigastric pain. Abdominal computed tomography revealed a pancreatic pseudocyst and a previously identified duplication of the esophagus, stomach, and duodenum with situs inversus totalis. The patient underwent esophagogastroduodenoscopy (EGD) with endoscopic ultrasonography for pseudocyst drainage. During EGD, a bifurcation of the esophagus was found. Duplication of the esophagus, stomach, and first part of the duodenum was evident on further advancement. A week later, there was repeated filling of the pseudocyst with a liquid component, and the patient underwent cystogastrostomy with stenting. Five months after discharge, the stent was removed without complications. CONCLUSIONS Duplication of the gastrointestinal tract and situs inversus totalis are very rare congenital malformations that require early diagnosis. While situs inversus totalis does not represent any medical disadvantage, physicians should be aware of abnormal anatomy before procedures to prepare specialists for this in case of the need for special techniques. Endoscopic treatment of pancreatic pseudocysts is safe and effective even in such rare cases. The use of endoscopic methods also minimizes intervention and decreases the length of the patients' stays in the hospital.

المؤلفون: English C; Pediatric and Adult Cardiology, UC Davis Medical Center, Sacramento, California, USA., Fan D; Pediatric and Adult Cardiology, UC Davis Medical Center, Sacramento, California, USA., Ing F; Pediatric and Adult Cardiology, UC Davis Medical Center, Sacramento, California, USA., Cortez D; Pediatric and Adult Cardiology, UC Davis Medical Center, Sacramento, California, USA.

المصدر: Journal of cardiovascular electrophysiology [J Cardiovasc Electrophysiol] 2024 Mar; Vol. 35 (3), pp. 418-421. Date of Electronic Publication: 2024 Jan 11.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Blackwell Country of Publication: United States NLM ID: 9010756 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1540-8167 (Electronic) Linking ISSN: 10453873 NLM ISO Abbreviation: J Cardiovasc Electrophysiol Subsets: MEDLINE

مواضيع طبية MeSH: Double Outlet Right Ventricle*/etiology , Pacemaker, Artificial*/adverse effects , Dextrocardia*, Male ; Humans ; Adult ; Cardiac Pacing, Artificial/adverse effects ; Heart Ventricles ; Treatment Outcome ; Equipment Design

مستخلص: Introduction: Patients with congenital heart disease are at increased risk for requiring cardiac pacing during their lifetime.
Methods: We present the first described case of using two leadless pacing systems manufactured by separate companies implanted within the same patient to provide atrial and ventricular pacing due to complex congenital anatomy.
Results: A 27-year-old male with dextrocardia with double outlet right ventricle, subaortic ventricular septal defect, and pulmonary stenosis status-post pulmonary valve replacement complicated by ventricular pacing dependence and subsequent atrial pacing dependence after atriotomy-based atypical flutter ablation developed recurrent mediastinitis and pocket infection with erosion despite prolonged antibiotic treatment. Due to atrial and ventricular pacing dependence, a comprehensive congenital care team concluded the need for lead extraction and replacement of pacemaker via leadless peacemaking device. Laser-lead extraction and temporary atrial pacemaker placement was performed. Afterward, a transesophageal echocardiogram guided implantation of both a Micra AV 2 (Medtronic) leadless pacemaker in the interventricular septum within the right ventricle and an Aveir (Abbott) leadless pacemaker in the superior base of the right atrial appendage was performed with successful pacing. Although there is no communication between these devices, atrial-mechanical ventricular pacing was reliable with good implant thresholds, impedances and sensing from both devices.
Conclusion: Our case demonstrates the feasibility of using dual leadless pacing modalities to simultaneously pace someone at complex, prohibitive risk for temporary permanent or permanent pacemaker devices.
(© 2024 The Authors. Journal of Cardiovascular Electrophysiology published by Wiley Periodicals LLC.)