This report describes the novel sampling of bile from the biliary endoscopic intervention for the molecular identification of parasite infection. A 63-year-old Vietnamese man underwent travel health examination in our hospital. Physical examination showed that his height was 159 cm and weight was 41 kg. He had a 15-year history of intermittent abdominal pain and frequent episodes of diarrhea. Laboratory tests revealed raised eosinophil count (23%, normal range [NR] 0-5), absolute eosinophil count (1899/mL, NR 50-350), and levels of serum immunoglobulin E (3770 IU/mL, NR<100), aspartate transaminase (270 U/L, NR 0-37), alanine transaminase (210 U/L, NR 0-40), and total bilirubin (1.8 mg/dL, NR 0.2-1.4); however, the serum alkaline phosphatase level was normal (65 U/L, NR 28-94) and non-reactive result for serum human insufficiency virus antibody. Magnetic resonance cholangiopancreatography revealed diffuse dilatation of the biliary tree; the common hepatic and pancreatic duct diameters increased to 1.86 cm and 0.61 cm, respectively. Endoscopic retrograde cholangiopancreatography was performed and a 10-Frmodel plastic biliary stent was inserted and flushed with 20 cc normal saline; thereafter, the bile was collected and sent for DNA sequencing. Isospora belli (IB) infection was identified by a polymerase chain reaction. Trimethoprim-sulfamethoxazole 800mg q6h was administered for 1 month. Liver enzyme levels normalized and negative for concentration method of ova study. The patient was doing well and weighed 51 kg at the outpatient clinic visit 3 months later. This bile sampling with molecular identification has not been described in the literature. We believe that an acute IB infection through fecal-oral transmission may progress to chronic infection of the hepatobiliary system, leading to biliary obstruction and jaundice.
CITATION STYLE
Chiu, K. W., Chiou, S. S., Lu, L. S., Wu, C. K., & Eng, H. L. (2016). Molecular identification of biliary isospora belli: A case report. Medicine (United States), 95(10). https://doi.org/10.1097/MD.0000000000003071
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