Results 61 to 70 of about 7,207 (227)

Value of serum GGT level in the timing of diagnosis of choledochal cyst perforation

open access: yesFrontiers in Pediatrics, 2022
BackgroundCholedochal cyst perforation is extremely rare, and early diagnosis or prediction is important for the immediate therapeutic intervention of perforations.
Shuhao Zhang   +9 more
doaj   +1 more source

Outcome of fetal ovarian cysts following in‐utero aspiration vs expectant management: multicenter cohort study

open access: yesUltrasound in Obstetrics &Gynecology, Volume 67, Issue 1, Page 60-66, January 2026.
ABSTRACT Objective The primary aim was to evaluate pre‐ and postnatal morphological changes in large simple fetal ovarian cysts following in‐utero aspiration compared with expectant management. Secondary aims were to assess postnatal outcome in terms of surgical intervention and to evaluate complications associated with in‐utero aspiration.
V. Peyronnet   +10 more
wiley   +1 more source

Choledochal cyst--case report [PDF]

open access: yes, 2012
Neðst á síðunni er hægt að nálgast greinina í heild sinni með því að smella á hlekkinn View/Open Allur texti - Full textThe clinical manifestation of a choledochal cyst is diverse and can mimic common diseases like gallstones, cholecystitis or ...
Karl Kristinsson   +2 more
core  

Choledochal Cyst

open access: yes, 2014
Choledochal cyst, which is characterized by dilatation of the biliary ducts, is common in Asian countries, mainly Japan, but relatively rare worldwide. This report describes 2 Saudi female children with choledochal cysts, with emphasis on long term follow-up.
openaire   +2 more sources

Pelvi‐Ureteric Junction Obstruction in a Solitary Functioning Kidney in Children: An Unfavourable Combination

open access: yesActa Paediatrica, Volume 115, Issue 1, Page 196-201, January 2026.
ABSTRACT Aim Solitary functioning kidney (SFK) is linked to chronic kidney disease (CKD) in children, particularly when associated with congenital anomalies of the kidney and urinary tract (CAKUT). Pelvi‐ureteric junction obstruction (PUJO) is the most frequent obstructive uropathy in SFK.
Mathilde Grapin   +9 more
wiley   +1 more source

Understanding the Operative Experience of the Practicing Pediatric Surgeon: Implications for Training and Maintaining Competency [PDF]

open access: yes, 2016
Importance The number of practicing pediatric surgeons has increased rapidly in the past 4 decades, without a significant increase in the incidence of rare diseases specific to the field.
Abdullah, Fizan   +15 more
core   +1 more source

Biliary Reconstruction for Intrahepatic Bile Duct Strictures and Optimal Jejunal Limb Length in Congenital Biliary Dilation Surgery: A Literature Review and Consensus Statements From the AOB Consensus Meeting

open access: yesAsian Journal of Endoscopic Surgery, Volume 19, Issue 1, January/December 2026.
ABSTRACT Introduction With the aim of facilitating cross‐specialty discussion on detailed anatomical interpretations in congenital biliary dilatation surgery, the Japan Society for Endoscopic Surgery (JSES) and the Consensus Meeting of Anatomy on the Border (AOB) developed a series of consensus statements in 2024.
Masahiro Takeda   +20 more
wiley   +1 more source

Diagnostic dilemma in a large choledochal cyst

open access: yesJournal of Society of Surgeons of Nepal, 2019
Choledochal cysts are rare congenital anomalies that have a variable presentation with occasional diagnostic and therapeutic dilemmas. Our case is a 14-year female presented with recurrent abdomen pain with confusing diagnostic findings, suggestive of
Tul Maya Gurung   +2 more
doaj   +1 more source

Congenital biliary anomaly with secondary cholangiohepatitis in a Siamese cross kitten [PDF]

open access: yes, 2016
A 5-month-old Siamese cross kitten was presented with jaundice and a palpable abdominal mass at the right cranial quadrant. The extra-hepatic biliary system was markedly distended upon abdominal ultrasonography.
Khor, Kuan Hua   +5 more
core  

Liver transplantation for biliary atresia [PDF]

open access: yes, 1984
Orthotopic liver transplantation was performed 15 months to 20 years ago in 126 recipients, all of whom were under 18 years of age. Eighty-six of these pediatric recipients were treated before 1980 with azathioprine (or eyclophosphamide) and prednisone ...
B.W. Shaw Jr.   +12 more
core   +2 more sources

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