Type II Abernethy malformation with cystic fibrosis in a 12-year-old girl: A case report

Figure 1 Chest and abdominal computed tomography. A and B: Chest computed tomography (CT) showed bronchial dilatation and flocculent shadow with multiple cystic translucency in both lungs; C-E: Preoperative whole abdominal enhanced CT showed splenomegaly, multiple tortuous dilated vessels at the splenic hilum, irregular liver morphology and pancreatic atrophy; F and G: 17-month postoperative whole abdomen enhanced CT showed irregular liver morphology, splenomegaly, multiple tortuous dilated vessels at the splenic hilum, and pancreatic atrophy.

Figure 2 CFTR gene sequencing. A: The mother of the proband was a carrier of CFTR gene c.233_c.234insT heterozygous mutation compared with the standard sequence; B: The father of the proband carried CFTR gene c.2909G>A/p.Gly970Asp heterozygous mutation.

Figure 3 Pathology of liver biopsy. Pathological findings of the liver biopsy showed poorly developed, dilated or absent portal vein branches.