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Updated: Apr 14, 2026

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Derivation of Hematopoietic Stem Cells from Murine Embryonic Stem Cells
Published on: February 25, 2007
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A Rare Complication Developing After Hematopoietic Stem Cell Transplantation: Wernicke's Encephalopathy
Soner Solmaz1, Çiğdem Gereklioğlu, Meliha Tan
1Adana Hospital of Başkent University, Department of Hematology, Adana, Turkey Phone: +90 322 327 27 27
Summary
Thiamine deficiency can cause Wernicke's encephalopathy, a rare central nervous system disorder. This case highlights its occurrence after hematopoietic stem cell transplantation in an acute myeloid leukemia patient receiving total parenteral nutrition.
Area of Science:
- Neurology
- Hematology
- Nutritional Science
Background:
- Thiamine (vitamin B1) is essential for neurological function.
- Thiamine deficiency leads to Wernicke's encephalopathy, characterized by confusion, ataxia, and ophthalmoplegia.
- This neurological complication is infrequently associated with hematopoietic stem cell transplantation (HSCT).
Purpose of the Study:
- To report a rare case of Wernicke's encephalopathy.
- To describe the presentation in a patient undergoing haploidentical allogeneic HSCT for acute myeloid leukemia (AML).
- To emphasize the potential role of prolonged total parenteral nutrition (TPN) in thiamine deficiency post-HSCT.
Main Methods:
- Case report of a patient with AML.
- Detailed clinical observation and treatment course following haploidentical allogeneic HSCT.
- Review of literature regarding Wernicke's encephalopathy post-HSCT and TPN.
Main Results:
- The patient developed classic symptoms of Wernicke's encephalopathy.
- The condition occurred during prolonged TPN after haploidentical allogeneic HSCT for AML.
- This represents the first reported case from Turkey.
Conclusions:
- Wernicke's encephalopathy is a rare but significant neurological complication that can occur after HSCT.
- Prolonged TPN may increase the risk of thiamine deficiency in HSCT recipients.
- Early recognition and thiamine supplementation are crucial for managing this condition in at-risk patients.
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