منابع مشابه
Characteristic prenatal ultrasonographic findings of patent urachus: a case report.
A characteristic prenatal ultrasonographic finding of patent urachus is described. Routine obstetrical ultrasonography first revealed a cystic mass in the umbilical cord at 16 weeks of gestation. The mass spontaneously decreased in size and was undetectable at full term on serial ultrasound examination. The male newborn infant was delivered uneventfully at 38 weeks of gestation, weighing 2,774 ...
متن کاملUltrasonographic diagnosis and minimally invasive treatment of a patent urachus associated with a patent omphalomesenteric duct in a newborn
RATIONAL Patent urachus (PU) is due to an incomplete obliteration of the urachus, whereas patent omphalomesenteric duct (POMD) is due to an incomplete obliteration of the vitelline duct. These anomalies are very rarely associated with one another. We describe a case of a newborn with a PU associated with a POMD, who was diagnosed by an abdominal ultrasound (US) and laparoscopy, and managed with...
متن کاملHepatoid Adenocarcinoma of the Urachus
Hepatoid adenocarcinoma of the urachus is a rare condition. We present the case of a 51-year-old female who developed abdominal pain and hematuria. Pelvic magnetic resonance imaging (MRI) reported an urachal mass with invasion to the bladder that was resected by partial cystectomy. On light microscopy the tumor resembled liver architecture, with polygonal atypical cells in nest formation and tr...
متن کاملUrachal bladder in kidney transplanted patient with Prune Belly syndrome and patent urachus.
We report a 16-year-old-male patient with Prune-Bellysyndrome (PBS) and patent urachus, bilateral renal dysplasia and end-stage renal disease (ESRD). The first kidney transplantation was performed at the age of 3 years, leaving an urachal catheter. Transplant failure underwent in a new cadaveric transplant at the present. Post-kidney transplant renogram was performed to evaluate the renal funct...
متن کاملHypertrophic Pyloric Stenosis developing In a Patient Operated for Patent Urachus – A Case Report
A neonate with patent urachus (PU) who later developed hypertrophic pyloric stenosis (HPS) is being reported. The newborn was first operated for PU; post-operatively he developed persistent vomiting and radiological workup confirmed HPS. Pyloromyotomy was performed with an uneventful recovery.
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ژورنال
عنوان ژورنال: BMJ
سال: 1875
ISSN: 0959-8138,1468-5833
DOI: 10.1136/bmj.2.772.486