Results 171 to 180 of about 375,643 (212)
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Umbilical cyst associated with patent urachus that spontaneously disappeared: A case report

Prenatal Diagnosis, 2021
A 31‐year‐old woman was referred to our hospital due to an umbilical cyst at 28 weeks of pregnancy. The cyst appeared to be fluid‐filled, was 65 35 mm in diameter and the umbilical cord was clearly edematous.
Yuya Fujibe, Tasuku Mariya, M. Mizuuchi
semanticscholar   +1 more source

Adult patent urachus presenting with umbilical discharge: a rare case report

International Surgery Journal
The urachus is a vestigial remnant of the allantoic duct, which normally regresses before birth to form the median umbilical ligament. Incomplete obliteration results in urachal anomalies, among which patent urachus is the most severe and rarest form ...
Lutfiya F. Bastawala   +2 more
semanticscholar   +1 more source

Patent urachus with bladder eversion

Journal of Pediatric Surgery, 2003
An infant was born at term after having received a diagnosis of omphalacele on prenatal ultrasound scan. She did not have an omphalacele but rather had a patent urachus with bladder eversion onto the abdominal wall. The remainder of the genitourinary tract was normal, and it was possible to pass a soft catheter through the urethra and out of the ...
Melania, Yeats, Lewis, Pinch
openaire   +2 more sources

Ectopic scrotum and patent urachus

Pediatric Surgery International, 2001
Ectopic scrotum is a rare condition and has been reported in association with other urological abnormalities. We present a case with an associated patent urachus and a brief discussion on the possible mechanism to explain this deformation.
S K, Chowdhary   +3 more
openaire   +2 more sources

Allantoic cyst and patent urachus

The Indian Journal of Pediatrics, 2008
Allantoic cysts of the umbilical cord are extremely rare anomalies. Only few cases have been reported in the postnatal life. The etiopathogenesis is still obscure. We describe a case of allantoic cyst and patent urachus in a newborn associated with hypospadias and meatal obstruction.
Kamalesh, Pal   +2 more
openaire   +2 more sources

Nonoperative management of a patent urachus

Urology, 2005
Patent urachus accounts for 10% to 15% of all reported urachal abnormalities in the literature. Treatment in the past has relied on immediate surgery. Conservative therapy with bladder catheter drainage, resulting in spontaneous closure, has not been described.
Scott P, Cuda   +2 more
openaire   +2 more sources

Laparoscopic Excision of a Patent Urachus

2008
Urachus extends from the dome of bladder to the umbilicus. It has three distinct layers. Incomplete obliteration of the urachus manifests in various forms (i.e.) urachal cyst, urachal sinus, urachal diverticulum and patent urachal fistula. Symptomatic urachal cyst and patent urachal fistula warrant surgical excision and can be accomplished ...
Kallappan Senthil, Manickam Ramalingam
openaire   +1 more source

Patent Urachus in the Adult

Australian and New Zealand Journal of Surgery, 1970
The urachus is a developmental tube between the bladder and umbilicus which normally undergoes closure prior to birth. Its failure to close leads to congenital anomalies, usually presenting in the neonate, but rarely in the adult. Two such adult cases are presented, and the embryology, clinical features, diagnosis and treatment are discussed.
openaire   +2 more sources

Laparoscopic Excision of a Patent Urachus

Surgical Laparoscopy, Endoscopy & Percutaneous Techniques, 1994
We report the case of a patent urachus presenting as an umbilical discharge. The urachus was visualised laparoscopically, divided at either extremity, and successfully removed with subsequent abrogation of symptoms.
H P, Redmond   +3 more
openaire   +2 more sources

Patent urachus

2016
Patent urachus is a congenital anomaly which results from the failure of the obliteration of the ventral aspect of the cloaca. Careful history and physical examination usually suffice to make the diagnosis. A neonate with patent urachus is presented, diagnostic and therapeutic implications are discussed.
Balik, E., Ulman, İ., Avanoglu, A.
openaire   +1 more source

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