A Rare Congenital Anomaly of the Gallbladder – Fundic Diverticulum
نویسنده
چکیده
Diverticulum of the human gall bladder is an important but distinct anatomical entity. Gallbladder diverticulum is an unusual and uncommon congenital anomalies that is rarely reported in the literature. We describe a patient with cholecystitis associated with a true gallbladder diverticulum was detected after surgery and confirmed histopathologically.
منابع مشابه
Embryological Basis and Clinical Correlation of the Rare Congenital Anomaly of the Human Gall Bladder: - “The Diverticulum” - A Morphological Study Key words: Gallbladder, Diverticulum, Congenital, Solitary, Cadaveric, Morphology
IntrOductIOn Diverticulum of the gall bladder is an important but distinct anatomical entity with significant clinical implications. Congenital diverticulum of the gall bladder is one of the rarest of all anomalies, corroborated by its very low incidence and infrequent reports and references in the literature [1]. Diverticulum can be of congenital or acquired variety. The congenital type contai...
متن کاملAnterior Urethral Valve and Diverticulum in a Neonate with Urinary Tract Infection
Introduction:Anterior urethral valve (AUV) is a rare congenital anomaly that can cause obstructive uropathy. AUV can lead to variable urinary tract symptoms, and if left untreated, it can result in end-stage renal disease. AUV should be immediately evaluated and managed. Herein, we present a neonate with AUV and diverticulum, who was treated by cystoscopy. Case report:A 11-day-old boy was ref...
متن کاملGallbladder Duplication: Case Report of a Rare Congenital Anomaly Treated by Single-Incision Laparoscopic Cholecystectomy in a Pediatric Patient
Introduction: Gallbladder duplication is a rare congenital anomaly. Preoperative diagnosis is essential for prevention of intra operative complications. Based on our review of the literature, this is the second description of gallbladder duplication treated with single-incision laparoscopic surgery (SILS). Case Presentation: A 14 year-old girl presented to the pediatric surgery clinic with a 4-...
متن کاملA Choledochal Cyst Resulting in Obstructive Jaundice in a Case with Gallbladder Agenesis: Report of a Case and Review of the Literature
Agenesis of the gallbladder (AGB) and choledochal cyst (CC) are among the rare conditions of congenital extrahepatic biliary tree anomalies. AGB results from the failure of the cystic bud to develop in the 4th week of intrauterine life. It normally develops from the caudal part of the hepatic diverticulum (1, 2). CCs are single or multiple dilatations of the intrahepatic or extrahepatic biliary...
متن کاملA Case of Double Gallbladder with Adenocarcinoma Arising from the Left Hepatic Duct: A Case Report and Review of the Literature
Double gallbladder is a rare congenital biliary anomaly, but an accessory gallbladder arising from the left hepatic duct is a more remarkably rare congenital anomaly. We report a case of double gallbladder with adenocarcinoma and gallstones, which was preoperatively diagnosed by endoscopic retrograde cholangiopancreatography (ERCP) and then confirmed by open laparotomy. A review of the literatu...
متن کامل