1928
DOI: 10.1097/00000658-192807000-00010
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Congenital Absence of the Gall-Bladder

Abstract: CONGENITAL ABSENCE OF THE GALL-BLADDER. to ^art fr?m congenital peculiarities of fixation, which predispose 0 volvulus of the gall-bladder, the organ may be double, bilobed r absent. The case of a ii-gravida, aged 26, in whom there was ^?ngenital absence of the gall-bladder is reported by Professor Le Fort. e had experienced normal parturition and puerperium three years Previously, and was again three months pregnant when, following

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Cited by 18 publications
(4 citation statements)
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“…Gallbladder agenesis without extrahepatic biliary atresia is a rare congenital anomaly. Since this abnormality was first described in 1701, several cases have been reported, and most cases of gallbladder agenesis have been asymptomatic . Preoperative diagnosis of gallbladder agenesis has been considered very difficult because abdominal ultrasonography (US) or computed tomography (CT) may not distinguish an absent gallbladder from one shrunken by inflammation.…”
Section: Introductionmentioning
confidence: 99%
“…Gallbladder agenesis without extrahepatic biliary atresia is a rare congenital anomaly. Since this abnormality was first described in 1701, several cases have been reported, and most cases of gallbladder agenesis have been asymptomatic . Preoperative diagnosis of gallbladder agenesis has been considered very difficult because abdominal ultrasonography (US) or computed tomography (CT) may not distinguish an absent gallbladder from one shrunken by inflammation.…”
Section: Introductionmentioning
confidence: 99%
“…Congenital gallbladder agenesis is a very rare situation [1][2][3]. Low clinical suspicion and inability of routine investigation to demonstrate this situation often leads to misdiagnosis and to a stressful procedure for the laparoscopic surgeon [14].…”
Section: Resultsmentioning
confidence: 99%
“…Most individuals remain asymptomatic for life. This abnormality was described in 1701 [3] and since 2003, 413 cases have been reported in the literature [4]. To date, more than 10 new cases have been reported [5-10].…”
Section: Introductionmentioning
confidence: 99%
“…Agenesis of the gallbladder and cystic duct is a rare congenital condition that results from the failure of the cystic bud to develop in the 4 th week of intrauterine life, and it has a reported incidence of 13–65 per 100 000 population [ 3 ]. It was first described in 1701 [ 4 ]. Choledocholithiasis has been reported to occur in 18% to 50% of patients with gallbladder agenesis, and all have jaundice as the first presentation [ 5 – 9 ].…”
Section: Introductionmentioning
confidence: 99%