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Published on: August 1, 2018
Hemodialysis-related portal-systemic encephalopathy
Naohide Kondo1, Yasuhiro Ito, Hiroshi Yamashita
1Department of Neurology, Nagoya University Graduate School of Medicine, Japan.
Hemodialysis-related portal-systemic encephalopathy (HRPSE) is a rare condition causing brain dysfunction without liver issues. This case highlights HRPSE as a treatable neuropsychiatric disorder, emphasizing prompt diagnosis and intervention.
Area of Science:
- Nephrology
- Neurology
- Gastroenterology
Background:
- Hemodialysis-related portal-systemic encephalopathy (HRPSE) presents as portosystemic encephalopathy without underlying liver dysfunction.
- It is typically associated with alterations in systemic venous flow secondary to hemodialysis procedures.
Observation:
- A 75-year-old woman experienced hepatic encephalopathy five years into her hemodialysis treatment.
- Diagnostic imaging, including contrast-enhanced CT and 3D CT angiography, identified an acquired portosystemic venous shunt.
Findings:
- The patient was diagnosed with portosystemic encephalopathy attributed to hemodialysis.
- Subsequent occlusion therapy effectively resolved the patient's disturbance of consciousness.
Implications:
- HRPSE represents a distinct, treatable cause of neuropsychiatric symptoms in hemodialysis patients.
- Recognition of HRPSE is crucial for timely and effective management, improving patient outcomes.
- This case underscores the importance of considering vascular complications in patients undergoing long-term hemodialysis.
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