Results 171 to 180 of about 37,403 (228)
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Acta Chirurgica Belgica, 2023
A 34-year-old man without previous medical history was admitted for right hypochondrium pain with nausea and vomiting. Blood tests were normal and abdominal echography described a difficult to find gallbladder but suspected biliary lithiasis. The diagnosis of uncomplicated symptomatic cholelithiasis was proposed and laparoscopic cholecystectomy was ...
Neuberg, Maud, Detry, Olivier
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A 34-year-old man without previous medical history was admitted for right hypochondrium pain with nausea and vomiting. Blood tests were normal and abdominal echography described a difficult to find gallbladder but suspected biliary lithiasis. The diagnosis of uncomplicated symptomatic cholelithiasis was proposed and laparoscopic cholecystectomy was ...
Neuberg, Maud, Detry, Olivier
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European Respiratory Journal, 1989
Agenesis of the lung is extremely rare. Developmental defects of the lung are usually associated with other congenital malformations. Half of all reported patients die either at birth or within the first 5 yrs of life. We report a case of right lung agenesis with absence of the left kidney, and fusion anomaly between ribs 4 and 5 on the left hemithorax.
KAYA, IS, DILMEN, U
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Agenesis of the lung is extremely rare. Developmental defects of the lung are usually associated with other congenital malformations. Half of all reported patients die either at birth or within the first 5 yrs of life. We report a case of right lung agenesis with absence of the left kidney, and fusion anomaly between ribs 4 and 5 on the left hemithorax.
KAYA, IS, DILMEN, U
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Journal of Pediatric Surgery, 1989
We report a case of agenesis of the trachea type III of Floyd that survived for 2 days with an esophageal intubation. Surgical treatment consisted of a distal esophageal binding, cervical esophagostomy in double-barrelled shotgun, and gastrostomy. Death occurred on the third day after surgery.
J, Rovira +5 more
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We report a case of agenesis of the trachea type III of Floyd that survived for 2 days with an esophageal intubation. Surgical treatment consisted of a distal esophageal binding, cervical esophagostomy in double-barrelled shotgun, and gastrostomy. Death occurred on the third day after surgery.
J, Rovira +5 more
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Annals of Otology, Rhinology & Laryngology, 1992
Tracheal agenesis is a catastrophic congenital anomaly that invariably results in death. Forty-seven cases have been previously reported in the literature. We add five additional cases, including two type 1 cases, two type 2 cases, and one type 3 case, based on Floyd's classification scheme.
P J, Koltai, R, Quiney
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Tracheal agenesis is a catastrophic congenital anomaly that invariably results in death. Forty-seven cases have been previously reported in the literature. We add five additional cases, including two type 1 cases, two type 2 cases, and one type 3 case, based on Floyd's classification scheme.
P J, Koltai, R, Quiney
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Acta Paediatrica, 1994
Complete agenesis of pancreas is a rare and lethal condition. Four cases have previously been reported in combination with other malformations, such as severe intrauterine growth retardation, hyperglycaemia and meconium ileus. We report a case of pancreatic agenesis as a single anomaly. The child died when 48 h old with severe metabolic acidosis.
P, Voldsgaard +2 more
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Complete agenesis of pancreas is a rare and lethal condition. Four cases have previously been reported in combination with other malformations, such as severe intrauterine growth retardation, hyperglycaemia and meconium ileus. We report a case of pancreatic agenesis as a single anomaly. The child died when 48 h old with severe metabolic acidosis.
P, Voldsgaard +2 more
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Southern Medical Journal, 1990
Tracheal agenesis is a rare congenital anomaly. We report a case and review the cases previously reported. Clinical features that might indicate tracheal agenesis include antenatal polyhydramnios, severe respiratory distress, absence of an audible cry, failure to advance an endotracheal tube beyond the larynx, a palpable distal trachea, clinical ...
T, Chiu +3 more
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Tracheal agenesis is a rare congenital anomaly. We report a case and review the cases previously reported. Clinical features that might indicate tracheal agenesis include antenatal polyhydramnios, severe respiratory distress, absence of an audible cry, failure to advance an endotracheal tube beyond the larynx, a palpable distal trachea, clinical ...
T, Chiu +3 more
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American Journal of Roentgenology, 1975
Tracheal agenesis is a rare anomaly that produces neonatal respiratory distress and has been uniformly lethal to date. In this malformation the entire trachea is usually absent, air reaching the bronchi through a communication with the esophagus, and the lungs are normally formed.
E L, Effmann +4 more
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Tracheal agenesis is a rare anomaly that produces neonatal respiratory distress and has been uniformly lethal to date. In this malformation the entire trachea is usually absent, air reaching the bronchi through a communication with the esophagus, and the lungs are normally formed.
E L, Effmann +4 more
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International Urology and Nephrology, 1988
Agenesis of the bladder is an extremely rare anomaly with only approximately 40 such cases reported in the literature. We report on a 30-year-old female patient who also had right renal agenesis.
A, Akdaş +3 more
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Agenesis of the bladder is an extremely rare anomaly with only approximately 40 such cases reported in the literature. We report on a 30-year-old female patient who also had right renal agenesis.
A, Akdaş +3 more
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International Journal of Pediatric Otorhinolaryngology, 1987
Congenital anomalies of the tracheobronchial tree must be included in the differential diagnosis of children with symptoms of respiratory distress. Tracheal agenesis is a rare major congenital anomaly that has been uniformly fatal. Diagnosis requires a high index of suspicion utilizing roentgenographic and endoscopic examinations.
D B, Kearns, R H, Miller
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Congenital anomalies of the tracheobronchial tree must be included in the differential diagnosis of children with symptoms of respiratory distress. Tracheal agenesis is a rare major congenital anomaly that has been uniformly fatal. Diagnosis requires a high index of suspicion utilizing roentgenographic and endoscopic examinations.
D B, Kearns, R H, Miller
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