ABSTRACT
RATIONALE: Hemolysis induced by high dose ascorbic acid (AA) in patients with G6PD deficiency has been reported, but is rare. To our knowledge, this is the first reported case of a male with G6PD deficiency, coexpressed with cholecystolithiasis and cholecystitis, who developed extreme hemolysis and hyperbilirubinemia after receiving pharmacological doses ascorbic acid infusion. PATIENT CONCERNS: A 27-year-old man history with glucose-6-phosphate dehydrogenase deficiency was admitted to our hospital because of cholecystolithiasis and cholecystitis. He appeared with scleral jaundice and very deep colored urine after receiving pharmacological doses ascorbic acid infusion. DIAGNOSES: Clinical findings when combined with his medical history and various laboratory results confirmed the diagnosis as hemolysis and hyperbilirubinemia induced by ascorbic acid. INTERVENTIONS: The patient was treated with steroids, hepatoprotective drugs, and folic acid in addition avoidance of agents with known hemolysis risk (such as vitamin C). OUTCOMES: As a result, the patient's symptoms from hemolytic jaundice improved, hemoglobin remained stable, and the patient was discharged 11 days later. LESSONS: Clinicians should bear in mind the possibility that vitamin C exposure may result in hemolysis in patients with G6PD deficiency, especially in those with known severe disease.
Subject(s)
Ascorbic Acid/adverse effects , Glucosephosphate Dehydrogenase Deficiency/drug therapy , Jaundice/chemically induced , Adult , Cholecystitis/congenital , Cholecystolithiasis/congenital , Glucosephosphate Dehydrogenase Deficiency/complications , Humans , Hyperbilirubinemia/chemically induced , MaleABSTRACT
Acute cholecystitis in the neonate is rare and usually treated by cholecystectomy. A 1-day-old full-term girl had clinical and sonographic features of acute calculous cholecystitis. This was successfully managed nonoperatively with intravenous fluids and antibiotics, leading to complete resolution of the condition. The infant currently is thriving and asymptomatic with a sonographically normal biliary tree. Spontaneous resolution of cholelithiasis may occur in neonates, even in the presence of acute cholecystitis.
Subject(s)
Cholecystitis/therapy , Acute Disease , Cholecystitis/congenital , Cholecystitis/diagnostic imaging , Female , Gallbladder/diagnostic imaging , Humans , Infant, Newborn , UltrasonographyABSTRACT
What appears to be the first reported case of an otherwise-asymptomatic newborn with a mass in the right upper quadrant of the abdomen and no signs of biliary disease is presented. At exploration, acute acalculous cholecystitis was found, probably secondary to cystic duct obstruction.
