Caudal Duplication Syndrome: A Case Report of Challenging Imaging Findings and Management | ||
International Journal of Pediatrics | ||
مقاله 44، دوره 10، شماره 8، آبان 2022، صفحه 16614-16619 اصل مقاله (472.22 K) | ||
نوع مقاله: case report | ||
شناسه دیجیتال (DOI): 10.22038/ijp.2021.54433.4304 | ||
نویسندگان | ||
Masood Mahdavi Rashed1؛ Ahmad Mohammadipour2؛ Samaneh Najafi3؛ Malihe Seyedhoseini* 4 | ||
1Department of Radiology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad,Iran | ||
2Department of surgury,Akbar Hospital,Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran | ||
3Department of Radiology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad,Iran. | ||
4Islamic Republic of Iran, Khorasan Razavi,Mashhad, Emamreza Hospital,Mashhad,Iran | ||
چکیده | ||
Caudal duplication syndrome is a rare congenital disease caused by duplication of cloaca and notochord embryonic structures in various forms. The estimated prevalence of this syndrome is 1 per 100,000 births. A range of anomalies is observed in urinary and gastrointestinal tracts as well as in skeletal and neural structures of the spine and even limbs of these patients. Various factors such as genetic disorders and conjoined twinning have been mentioned in etiology of the disease. We introduce a case of this rare disease referred to our center for imaging as an infant with increased soft tissue in perineum without excretion of meconium from birth but with evidence of duplication in the genitourinary system (vagina and urethra) and gastrointestinal tract (rectum and colon) that was subject to reconstructive surgery. | ||
کلیدواژهها | ||
Caudal Duplication Syndrome؛ Congenital Anomalies؛ Genitourinary Duplication؛ Infant | ||
مراجع | ||
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آمار تعداد مشاهده مقاله: 334 تعداد دریافت فایل اصل مقاله: 294 |