A case of hereditary presacral teratoma involving father and daughter is described. The use of magnetic resonance imaging in the diagnosis of this condition is illustrated and a review of the literature of this unusual condition is presented.
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http://dx.doi.org/10.1111/j.1445-2197.1996.tb01224.x | DOI Listing |
Radiol Case Rep
December 2024
Department of Radiology, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia.
Diphallia, also known as penile duplication, represents a highly unusual congenital abnormality of sex development, occurring in 1 in every 5 million to 1 in thirty million live births. Wecker, in Bologna, Italy, noted the first instance of diphallia in 1609. Meanwhile, no sufficient report has meticulously described the incidence in Indonesia.
View Article and Find Full Text PDFRadiol Case Rep
September 2022
Chronic Respiratory Diseases Research Center, National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Currarino syndrome is an autosomal dominant hereditary disease defined as a triad of anorectal abnormality, sacral dysgenesis, and a presacral mass, primarily an anterior sacral meningocele. It is often seen in children and considered rare in adults. It is mostly found as an incidental finding.
View Article and Find Full Text PDFObstet Gynecol Sci
September 2019
Department of Obstetrics and Gynecology, Konkuk University School of Medicine, Seoul, Korea.
Currarino syndrome is a hereditary disease characterized by the triad of sacral agenesis, anorectal malformation, and presacral mass. Most patients are diagnosed in childhood, and this condition rarely manifests in adulthood. In women, gynecological malformations associated with Currarino syndrome have been reported, such as bicornuate uterus, rectovaginal fistula, and septate uterus.
View Article and Find Full Text PDFA A Pract
June 2019
From the Department of Anesthesiology and Perioperative Medicine, College of Medicine, Mayo Clinic, Rochester, Minnesota.
Currarino triad is a rare hereditary condition characterized by anorectal malformation, sacral dysgenesis, and a presacral mass. Neuraxial anesthetic techniques pose increased risks to patients with spinal malformations. Ultrasound imaging improves accuracy of intervertebral level identification compared to clinical estimation.
View Article and Find Full Text PDFInt J Surg Case Rep
March 2019
Department of Pediatric Surgery, Saint George Hospital University Medical Center, Balamand University, Beirut, Lebanon.
Introduction: Currarino syndrome is a rare congenital disorder characterized by a triad of anorectal malformation, a sacral bone defect, and a presacral mass. It results of an abnormal separation of the ectoderm from the endoderm caused by HLXB9 mutation in chromosome 7q36 in 50% of cases. The disorder is mostly hereditary as it can also be sporadic with a variable expression spectrum.
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