A case of mitochondrial encephalomyopathy remarkable presenting with refractory shock.
10.11817/j.issn.1672-7347.2025.240250
- Author:
Yang LIAO
1
,
2
;
Daomiao XU
1
;
Li LI
1
,
3
Author Information
1. Department of Critical Care Medicine, Xiangya Hospital, Central South University, Changsha
2. Liaoyang@csu.edu.cn.
3. 404620@csu.edu.cn.
- Publication Type:Case Reports
- Keywords:
abdominal pain;
hyperlactacidemia;
mitochondrial encephalomyopathy;
myasthenia;
refractory shock
- MeSH:
Humans;
Male;
Mitochondrial Encephalomyopathies/genetics*;
Mutation;
Shock/etiology*
- From:
Journal of Central South University(Medical Sciences)
2025;50(3):511-516
- CountryChina
- Language:English
-
Abstract:
Mitochondrial encephalomyopathy is a multisystemic metabolic disorder caused by mutations in mitochondrial or nuclear genes. It commonly presents with stroke-like episodes or myopathy as initial symptoms. This paper reports a young male patient with mitochondrial encephalomyopathy whose early and prominent clinical manifestation was refractory shock, without typical neurological symptoms. The patient initially presented with abdominal pain and lower limb weakness, followed by severe hypotension requiring high-dose vasopressors to maintain blood pressure. His lactate level peaked at 20 mmol/L. After 10 days of symptomatic and supportive treatment, his hypotension resolved; lactate levels returned to normal by day 22. One month later, he still had difficulty weaning from mechanical ventilation and exhibited persistent limb weakness. Genetic testing of the biceps brachii revealed an m.3271T>C mutation in the mitochondrial tRNA gene. Mitochondrial encephalomyopathy may initially present with severe circulatory dysfunction. In patients with lactic acidosis not related to hypoperfusion, mitochondrial disease should be considered, and genetic testing of muscle or other peripheral tissues may improve diagnostic yield.
