1,468 results match your criteria Situs Inversus Imaging

Transverse colon cancer with obstruction in a patient with situs inversus totalis: A case report and review of literature.

Asian J Surg 2020 Dec 28;43(12):1186-1188. Epub 2020 Sep 28.

Department of General Surgery, 900 Hospital of the Joint Logistics Support Force, Fuzhou General Hospital of Fujian Medical University, Fuzhou, China. Electronic address:

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December 2020

Prenatal Diagnosis of Isolated Atrioventricular Discordance and Ventriculoarterial Concordance and Double-Outlet Right Ventricle in Situs Inversus: Case Report and Review of the Literature.

Pediatr Cardiol 2020 Dec 24;41(8):1807-1810. Epub 2020 Sep 24.

Department of Pediatrics, Section of Pediatric Cardiology, Rush University Medical Center, Chicago, IL, USA.

Atrioventricular (AV) discordance and ventriculoarterial (VA) concordance in the setting of visceral situs inversus are one of the rarest forms of cardiac malformations. To our knowledge, this is the first reported case of prenatal diagnosis of such rare cardiac anatomy in association with double-outlet right ventricle on fetal echocardiography. The physiology of this cardiac anomaly is similar to that of transposition of the great arteries, and the best surgical option is the atrial switch operation. Read More

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December 2020

Unilateral Situs Inversus of the Optic Disc in a Patient With Retinal Arteriolar Tortuosity.

Ophthalmic Surg Lasers Imaging Retina 2020 09;51(9):533-535

Familial retinal arteriolar tortuosity (fRAT) is a rare autosomal dominant disorder that is characterized by tortuosity of the second- and third-order arterioles around the posterior pole of retina. Most cases with fRAT lack associated systemic vascular abnormality. Situs inversus, a congenital anomaly, features emergence of retinal vessels from the optic nerve head in a nasal direction, usually occurs bilaterally. Read More

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September 2020

Ex vivo cardiovascular magnetic resonance diffusion weighted imaging in congenital heart disease, an insight into the microstructures of tetralogy of Fallot, biventricular and univentricular systemic right ventricle.

J Cardiovasc Magn Reson 2020 09 21;22(1):69. Epub 2020 Sep 21.

Department of Anatomy and Medical Imaging, University of Auckland, Auckland, New Zealand.

Purpose: Common types of congenital heart disease exhibit a variety of structural and functional variations which may be accompanied by changes in the myocardial microstructure. We aimed to compare myocardial architecture from magnetic resonance diffusion tensor imaging (DTI) in preserved pathology specimens.

Materials And Methods: Pathology specimens (n = 24) formalin-fixed for 40. Read More

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September 2020

Assessment of Myocardial Viability Using Nuclear Medicine Imaging in Dextrocardia.

J Nucl Med Technol 2020 Dec 4;48(4):372-377. Epub 2020 Sep 4.

Department of Nuclear Medicine, King Edward Memorial Hospital, Seth G.S. Medical College, Mumbai, India.

Imaging of dextrocardia in humans requires an understanding of the orientation of the heart chambers and walls. There are many types of cardiac malpositioning, such as dextrocardia (with or without situs inversus), mesocardia, and levocardia. Myocardial perfusion scintigraphy of dextrocardia has been explained in case reports and imaging atlases; however, myocardial viability assessment using nuclear medicine imaging techniques is less documented in the literature. Read More

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December 2020

Co-occurrence of Moyamoya syndrome and Kartagener syndrome caused by the mutation of DNAH5 and DNAH11: a case report.

BMC Neurol 2020 Aug 26;20(1):314. Epub 2020 Aug 26.

Department of Neurology, Affiliated Hospital of Jining Medical University, 89 Guhuai Road, Jining City, 272029, Shandong Province, China.

Background: Kartagener syndrome is an autosomal recessive inherited disorder of primary ciliary dyskinesia. Moyamoya syndrome refers to a moyamoya angiopathy associated with other neurological and/or extra-neurological symptoms, or due to a well identified acquired or inherited cause. We herein reported a case of a 48-year-old woman who was favored the diagnosis of Kartagener syndrome and moyamoya syndrome. Read More

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[Right aortic arch with left descending aorta: a rare cause of dysphagia].

Pan Afr Med J 2020 13;36:17. Epub 2020 May 13.

Centre des Urgences de Yaoundé, Yaoundé, Cameroun.

Aortic abnormalities are a rare cause of dysphagia in children, adolescents, young adults and in the elderly. In these cases, vascular abnormalities commonly include aberrant right subclavian artery, left subclavian artery originating from the right aortic arch and, more rarely, from the right aortic arch with thoracic aorta on the left. Dysphagia, also known as "dysphagia lusoria", is due to the compression of the esophagus caused by one or several congenital vascular abnormalities and can occur in childhood or later in adulthood. Read More

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December 2020

Successful removal of multiple bile duct stones using a papillary large balloon dilation in a very elderly woman with situs inversus totalis.

Clin J Gastroenterol 2021 Feb 9;14(1):309-313. Epub 2020 Aug 9.

Department of Gastroenterology, South Miyagi Medical Center, 38-1 Aza-Nishi, Ohgawara, Miyagi, 989-1253, Japan.

Situs inversus totalis (SIT) is a rare congenital anomaly in which all viscera are transposed to the opposite side of the body. This uncommon anatomy causes technical difficulties in endoscopic treatment. A 98-year-old woman with SIT was admitted to our hospital complaining of upper abdominal pain and fever. Read More

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February 2021

Left bundle branch pacing in a patient with mirror image dextrocardia and persistent right superior vena cava.

Europace 2020 08;22(8):1215

Department of Cardiology, Guangdong Cardiovascular Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Science, Guangzhou, China.

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Small bowel obstruction with situs inversus abdominalis: A case report.

Int J Surg Case Rep 2020 15;73:307-309. Epub 2020 Jul 15.

Department of General Surgery, Armadale-Kelmscott Memorial Hospital, Australia.

Introduction: Situs inversus abdominalis (SIA) is an uncommon condition that causes intestinal malrotation in the paediatric population as its primary complication (Brown, 2017). Presentations of acute surgical emergencies in adults secondary to SIA are extremely rare (Brown, 2017).

Presentation Of Case: A 38-year-old female with situs inversus abdominalis (SIA) presented with small bowel obstruction (SBO). Read More

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An ST-Elevation Myocardial Infarction In Situs Inversus Totalis (DEXTROCARDIA).

J Emerg Med 2020 Oct 23;59(4):597-599. Epub 2020 Jul 23.

University of Chicago Pritzker School of Medicine, Chicago, Illinois; Division of Cardiology, NorthShore University HealthSystem, Chicago, Illinois.

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October 2020

A Huge Ovarian Mucinous Cystadenoma in a 15-Year-Old Girl with Situs Inversus Totalis: Report of a Rare Case.

J Pediatr Adolesc Gynecol 2021 Feb 18;34(1):88-91. Epub 2020 Jul 18.

Department of Tumour Surgery, Lanzhou University Second Hospital, Lanzhou, China. Electronic address:

Background: Ovarian mucinous cystadenomas with situs inversus totalis are infrequent in pubertal girls. Surgical techniques on their treatment without affecting ovary anatomical and physiological function have always been a great challenge.

Case: A 15-year-old girl presented with abdominal distension and pain due to some huge growths. Read More

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February 2021

Successful endovascular repair of aortic rupture caused by axillary intra-aortic balloon insertion for a Jehovah's Witness patient with situs inversus anomaly.

J Card Surg 2020 Sep 11;35(9):2410-2413. Epub 2020 Jul 11.

Department of Surgery, Section of Vascular Surgery and Endovascular Therapy, University of Chicago Medicine, Chicago, Illinois.

We report the successful endovascular repair of a rare case of aortic rupture caused by axillary intra-aortic balloon pump (IABP) insertion failure. A 38-year-old Jehovah's Witness female with situs inversus totalis was referred to our hospital for acute decompensated heart failure. We placed an axillary IABP for circulatory support. Read More

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September 2020

Thoracoatrial discordance in a case of twisted atrioventricular connections: A unique configuration of visceroatrial arrangement.

J Card Surg 2020 Oct 11;35(10):2798-2799. Epub 2020 Jul 11.

Department of Cardiovascular Radiology and Endovascular Interventions, All India Institute of Medical Sciences, New Delhi, India.

We present a case of a 12-year-old boy with discordance between the atrial arrangement and the thoracoabdominal arrangement in the setting of twisted atrioventricular connections. This case highlights the importance of a separate description of all visceral organs and venous drainage for an accurate description of visceroatrial arrangement in cases of congenital heart defects. Read More

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October 2020

Multimodal Imaging in a Case of Fovea Plana Associated with Situs Inversus of the Optic Disc

Turk J Ophthalmol 2020 06;50(3):190-192

University of Health Sciences Turkey, Ankara Ulucanlar Eye Training and Research Hospital, Clinic of Ophthalmology, Ankara, Turkey.

Fovea plana is a congenital condition characterized by anatomic absence of the foveal pit. It may be isolated or associated with congenital ocular anomalies. In this report, we present a case of fovea plana associated with situs inversus of the optic disc, optic disc hypoplasia, tilted optic disc, and prepapillary vascular loop and with best corrected visual acuity of 20/32. Read More

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A case report of late-onset symptoms of erythrocytosis in univentricular dextrocardia.

Medicine (Baltimore) 2020 Jul;99(27):e21092

Department of Ultrasound, Zhejiang Hospital, Hangzhou, China.

Rationale: Univentricular dextrocardia is a rare congenital heart disease that usually presents cyanotic manifestations from childhood. Due to the sustained dysfunction of blood oxygenation, it is very difficult to keep an asymptomatic survival. Herein, we described an interesting case of univentricular dextrocardia who suffered from initial symptoms in his middle age. Read More

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Percutaneous coronary intervention in dextrocardia: a case report and a brief review of the literature.

J Cardiovasc Med (Hagerstown) 2020 Aug;21(8):613-615

Interventional Cardiology Unit, Azienda Ospedaliera Universitaria di Parma, Parma, Italy.

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Unconventional deployment of atrial septal occluder in a patient with atrial septal defect, dextrocardia, and interrupted inferior vena cava.

Cardiol Young 2020 Aug 29;30(8):1206-1208. Epub 2020 Jun 29.

Department of Cardiology, Nizam's Institute of Medical Sciences, Hyderabad, India.

An atrial septal defect is a rare anomaly in patients with interrupted inferior vena cava, which renders the percutaneous intervention more complex; and hence, innovative approaches should be sought. Dextrocardia further complicates the procedure, and traditional atrial septal device deployment methods cannot be employed. We report a successful percutaneous secundum atrial septal defect closure by a novel deployment strategy along with balloon dilation of associated severe valvular pulmonary stenosis in a patient with dextrocardia and interrupted inferior vena cava. Read More

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Video-assisted minimally invasive aortic valve replacement through left anterior mini-thoracotomy in a patient with situs inversus totalis.

Eur J Cardiothorac Surg 2020 11;58(5):1095-1096

Division of Thoracic and Cardiovascular Surgery, Heart Centre Siegburg, Siegburg, Germany.

We describe herein the first experience with a surgical technique for aortic valve replacement using a video-assisted minimally invasive approach via a left anterior mini-thoracotomy in patient with dextrocardia and situs inversus totalis. This procedure was performed safely with good clinical and cosmetic results. Read More

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November 2020

Urgent cholecystectomy in patient with left-sided gallbladder Case report and review of the literature.

Ann Ital Chir 2020 May 25;9. Epub 2020 May 25.

Introduction: Sinistroposition of the gallbladder, or true left-sided gallbladder (LSG) without situs viscerum inversus, is a rare congenital anatomical variant where the gallbladder is located to the left of round/falciform ligament. It can be associated with anomalies of the biliary tree, portal system and hepatic vascularization. The surgical management of a LSG could be challenging even for an experienced operator, being usually an incidental intraoperative finding. Read More

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Double lung transplantation for end-stage Kartagener syndrome: a case report and literature review.

J Thorac Dis 2020 Apr;12(4):1588-1594

Department of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan 430060, China.

Kartagener syndrome (KS) is an autosomal recessive disorder characterized by situs inversus, paranasal sinusitis and bronchiectasis. We report the successful use of double lung transplant (DLTx) to treat end-stage KS. A 49-year-old Han woman was admitted to Renmin Hospital (Wuhan University, China) in September 2017 with a ≥15 year history of chronic productive cough that had worsened during the past year. Read More

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Cardiac herniation after blunt thoracic trauma.

CMAJ 2020 04;192(17):E454

Departments of Emergency Medicine (Broughton), Anesthesia (Maguire) and Thoracic Surgery (LeBlanc), Rady College of Medicine, University of Manitoba, Winnipeg, Man.

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Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report.

BMC Med Genet 2020 05 1;21(1):87. Epub 2020 May 1.

Department of Medicine, Solna, Karolinska Institutet, Solnavägen 30, 171 76 Solna, Stockholm, Sweden.

Background: Developmental dyslexia (DD) is a neurodevelopmental learning disorder with high heritability. A number of candidate susceptibility genes have been identified, some of which are linked to the function of the cilium, an organelle regulating left-right asymmetry development in the embryo. Furthermore, it has been suggested that disrupted left-right asymmetry of the brain may play a role in neurodevelopmental disorders such as DD. Read More

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Dextrocardia, situs solitus, inlet ventricular septal defect (VSD), and iatrogenic tricuspid regurgitation (TR)-A surgical perspective.

J Card Surg 2020 Jun 29;35(6):1383-1386. Epub 2020 Apr 29.

Department of Cardiovascular and Thoracic Surgery, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.

Dextrocardia with situs solitus is a rare congenital anomaly, often associated with intra- or extracardiac malformations. A clear understanding of the spatial orientation of the chambers of the heart for planning surgical approach, is imperative. Access to the right side of the heart, especially for repair of the tricuspid valve can be challenging. Read More

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Transposition of the Great Arteries Associated With Non-Kommerell Diverticulum: Lessons From Two Cases.

World J Pediatr Congenit Heart Surg 2020 May;11(3):377-379

Department of Cardiovascular Surgery, Children Heart Center, National Children's Hospital, Đống Đa, Hanoi, Vietnam.

Vascular ring malformations usually occur as an isolated lesion. d-Transposition of the great arteries (d-TGA) associated with vascular ring malformations has seldom been reported in the literature. In this report, we describe two unusual cases of d-TGA associated with non-Kommerell diverticulum resulting in vascular ring. Read More

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Kartagener Syndrome.

Am J Med Sci 2020 06 21;359(6):390-391. Epub 2020 Feb 21.

Department of Respiratory and Critical Care Medicine, West China School of Medicine and West China Hospital, Sichuan University, Chengdu, China. Electronic address:

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Beta-sitosterol-induced Acute Pancreatitis: A Case Report and Review of the Literature.

Cureus 2020 Mar 25;12(3):e7407. Epub 2020 Mar 25.

Gastroenterology, West Virginia University, Morgantown, USA.

While drug-induced pancreatitis from corticosteroids has been well described in the medical literature, the exact mechanism is unclear. We present the first reported case of drug-induced pancreatitis from beta-sitosterol, a naturally occurring plant sterol structurally similar to cholesterol, obtained primarily through Western diet and supplementation. A 57-year-old male with a history of situs inversus and benign prostatic hyperplasia presented from an outside facility with a two-day history of worsening epigastric pain radiating to the right upper quadrant. Read More

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