Hepatic Resection and Transplant in Glycogen Storage Diseases

Exp Clin Transplant. 2022 Jun;20(6):609-612. doi: 10.6002/ect.2019.0313. Epub 2020 Feb 7.

Abstract

Patients with glycogen storage diseases pose unique management challenges to clinicians.These challenges are exacerbated wheneverthey undergo surgery as the basic anomaly in their glycogen storage pathways make them susceptible to organic acidosis, which may in turn complicate their preoperative, intraoperative, and postoperative course. Because of the rarity of these diseases, clinicians may not be aware of the specific management concerns. In the case reported here, a 37-year-old patient with glycogen storage disease type 1 underwentleft hepatectomy for hepatic adenomatosis, which was complicated by intraoperative severe lactic acidosis that was successfully treated. After successful hepatectomy, the patient underwent liver transplant without major lactic acidosis or hemodynamic instability. Early recognition and aggressive management of blood sugar and lactic acidosis in patients with glycogen storage diseases can allow for successful outcomes even when complex surgical procedures are required.

Publication types

  • Case Reports

MeSH terms

  • Acidosis, Lactic*
  • Adult
  • Glycogen Storage Disease* / diagnosis
  • Glycogen Storage Disease* / surgery
  • Hepatectomy
  • Humans
  • Liver
  • Treatment Outcome