Porto-systemic shunt - a rare cause of hyperandrogenism in children. Two case reports and review of literature.
Mikołaj DankoAnna MalinowskaElżbieta MoszczyńskaJoanna PawłowskaMaria Szarras-CzapnikMałgorzata Walewska-WolfUrszula WątrobińskaMieczysław SzaleckiPublished in: Journal of pediatric endocrinology & metabolism : JPEM (2020)
Objectives The main cause of hyperandrogenism in children is congenital adrenal hyperplasia, adrenal and gonadal tumors, polycystic ovary syndrome (PCOs) and Cushing's disease. In the last 20 years several descriptions of girls with hyperandrogenism and venous porto-systemic shunts appeared in literature. Case presentation First case is an eleven and a half-year-old girl, was admitted to Department of Endocrinology because of symptoms of hyperandrogenism. Laboratory tests revealed high serum testosterone, androstenedione, and dehydroepiandrosterone sulfate (DHEAS). The ammonia concentration was also increased. In the abdominal angio-CT scans persistent umbilical vein which connected portal and femoral vein was found. The second case was a seven-year-old boy with symptoms of precocious puberty. Blood tests also revealed high concentration of testosterone, androstenedione, DHEAS and ammonia. Imaging studies showed persistent ductus venosus. Conclusion Although pathophysiological relation is not clear, porto-systemic shunts should be considered as a cause of hyperandrogenism of unknown origin in children.
Keyphrases
- polycystic ovary syndrome
- insulin resistance
- young adults
- computed tomography
- systematic review
- high resolution
- case report
- adipose tissue
- magnetic resonance
- magnetic resonance imaging
- contrast enhanced
- metabolic syndrome
- type diabetes
- room temperature
- skeletal muscle
- depressive symptoms
- image quality
- sleep quality
- dual energy
- pulmonary hypertension
- pulmonary artery
- pulmonary arterial hypertension