Results 21 to 30 of about 8,563 (214)

Intussusception in a child with situs inversus totalis – A rare occurrence

open access: yesJournal of Pediatric Surgery Case Reports, 2022
Intussusception is when section of bowel is drawn into another. It is considered the commonest cause of intestinal obstruction in children. It is associated with a favorable outcome when diagnosis and management are prompt.
Alex Osei Assim   +3 more
doaj   +1 more source

Situs inversus totalis with symptomatic cholelithiasis: A diagnostic dilemma

open access: yesCHRISMED Journal of Health and Research, 2019
Situs inversus is a rare autosomal recessive condition, with incidence that varies from 1 in 5000 to 1 in 20,000 live births. Because of the atypical “mirror-image” anatomy associated with situs inversus, diagnosis of gallstone disease in these patients ...
Vishal Bodh   +4 more
doaj   +1 more source

Video Documentary of Situs Inversus Totalis in a Male Cadaver Module 1: Initial Discovery of Situs Inversus Totalis

open access: yesMedEdPORTAL, 2014
Situs inversus totalis is a condition in which the internal organs of the human body are transposed to opposite sides. On average, 1 in 20,000 individuals has situs inversus totalis.
Gregory Casey, Lisa Campeau
doaj   +1 more source

Situs inversus with levocardia in a 15-year-old male adolescent: a case report

open access: yesJournal of Medical Case Reports, 2023
Background Situs inversus with levocardia is a rare anomaly in which the heart is present in the left chest but the abdominal viscera are transposed. It is caused by a single incomplete penetration of an autosomal recessive gene.
Telila Mesfin   +9 more
doaj   +1 more source

An unknown situs viscerum inversus totalis, accidentally discovered after computed tomography [PDF]

open access: yesDigital Diagnostics
Benign situs inversus totalis of the viscerum is often diagnosed accidentally, rarely in adults, and more frequently in children and neonates, affecting both sexes.
Manuela Montatore   +4 more
doaj   +1 more source

Laparoscopic hemicolectomy for a patient with situs inversus totalis and colorectal cancer

open access: yesJournal of Coloproctology, 2017
Situs inversus totalis is a congenital anatomic anomaly characterized by a complete inversion of thoracic and abdominal organs. We present a case of a 67 year-old patient diagnosed with situs inversus totals in his childhood who was referred for a two ...
Maria Labalde Martínez   +3 more
doaj   +1 more source

Avoiding misdiagnosis of duodenal papilla adenocarcinoma in a situs inversus totalis patient via laparoscopic pancreaticoduodenectomy: A rare case report

open access: yesFrontiers in Surgery, 2023
Situs inversus totalis is a rare congenital anatomical anomaly that causes some difficult problems for surgeons when performing an operation. However, without histopathology specimens from surgery, a misdiagnosis of cancer may be unavoidable, in addition
Hao Liang   +4 more
doaj   +1 more source

How standard transesophageal echocardiography views change with dextrocardia

open access: yesAnnals of Cardiac Anaesthesia, 2013
Dextrocardia with situs inversus is a rare condition. Situs inversus with dextrocardia is also called as "situs inversus totalis". Transesophageal echocardiography (TEE) views in dextrocardia patient are not discussed in the literature.
Monish S Raut   +3 more
doaj   +1 more source

Transumbilical Surgery for Duodenal Stenosis in a Child with Situs Inversus: The First Report

open access: yesCase Reports in Pediatrics, 2017
Background. Situs inversus is a rare congenital anomaly with a reported incidence of only 1 in 5,000 to 10,000 live births. Congenital duodenal stenosis complicated with situs inversus is an even rarer entity. Case Presentation.
Isamu Saeki   +4 more
doaj   +1 more source

Renal Cell Carcinoma in A Patient with Kartagener Syndrome: First Case Report in English Language

open access: yesJournal of Urological Surgery, 2015
Cardiac and pulmonary anomalies are common among patients with situs inversus totalis. Renal anomalies, including renal agenesis, dysplasia, hypoplasia, ectopia, polycystic kidney, and horseshoe kidney have been reported.
Erkin Sağlam   +5 more
doaj   +1 more source

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