Cargando…
Hepatic Encephalopathy Mimicking Creutzfeldt-Jakob Disease on Laboratory, Physiological, and Imaging Evaluations
Patient: Female, 84-year-old Final Diagnosis: Hepatic encephalopathy Symptoms: Cognitive impairment Medication:— Clinical Procedure: — Specialty: Neurology OBJECTIVE: Unusual clinical course BACKGROUND: Creutzfeldt-Jakob disease (CJD) is an irreversible, neurodegenerative, prion disease presenting w...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8392707/ https://www.ncbi.nlm.nih.gov/pubmed/34420027 http://dx.doi.org/10.12659/AJCR.932958 |
_version_ | 1783743565876166656 |
---|---|
author | Kimura, Masamune Kimura, Hideki Ishikawa, Hiroki Matsuo, Hisayasu Takada, Masahiko Matsuo, Koushun |
author_facet | Kimura, Masamune Kimura, Hideki Ishikawa, Hiroki Matsuo, Hisayasu Takada, Masahiko Matsuo, Koushun |
author_sort | Kimura, Masamune |
collection | PubMed |
description | Patient: Female, 84-year-old Final Diagnosis: Hepatic encephalopathy Symptoms: Cognitive impairment Medication:— Clinical Procedure: — Specialty: Neurology OBJECTIVE: Unusual clinical course BACKGROUND: Creutzfeldt-Jakob disease (CJD) is an irreversible, neurodegenerative, prion disease presenting with cognitive, behavioral, and motor dysfunction. The clinical presentations or laboratory findings of treatable autoimmune and metabolic processes may mimic those of CJD. Hepatic encephalopathy (HE) is a complication of severe hepatic failure that is characterized by neuropsychiatric manifestations. A case of HE whose laboratory, physiological, and imaging results were similar to that of Creutzfeldt-Jakob disease (CJD) in the process of treatment for HE is presented. CASE REPORT: An 84-year-old woman with hepatic encephalopathy (HE) was admitted to our hospital because of acute consciousness disturbance. She had chronic hepatitis type C, liver cirrhosis, and hepatocellular carcinoma, and had had an episode of HE once. Her severe consciousness disturbance did not improve after treatment for concurrent hyperammonemia, unlike in her previous episode. Diffusion-weighted brain magnetic resonance imaging (MRI) showed widespread hyperintensity of the whole cortex. Her electroencephalogram showed periodic sharp wave complexes (PSWCs). Both total t-tau and 14-3-3 proteins were detected in her cerebrospinal fluid. According to these clinical data, CJD was highly suspected. However, the consciousness disturbance was alleviated by the tenth day of admission, and her general condition was markedly improved, which supported the initial diagnosis of HE. CONCLUSIONS: The present results suggest that treatable disorders, such as HE, should be considered before making a final diagnosis of a fatal disease such as CJD, since the spectrum of diseases that CJD mimics is vast. We should also aggressively treat patients with severe conditions from which recovery is possible. |
format | Online Article Text |
id | pubmed-8392707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83927072021-09-03 Hepatic Encephalopathy Mimicking Creutzfeldt-Jakob Disease on Laboratory, Physiological, and Imaging Evaluations Kimura, Masamune Kimura, Hideki Ishikawa, Hiroki Matsuo, Hisayasu Takada, Masahiko Matsuo, Koushun Am J Case Rep Articles Patient: Female, 84-year-old Final Diagnosis: Hepatic encephalopathy Symptoms: Cognitive impairment Medication:— Clinical Procedure: — Specialty: Neurology OBJECTIVE: Unusual clinical course BACKGROUND: Creutzfeldt-Jakob disease (CJD) is an irreversible, neurodegenerative, prion disease presenting with cognitive, behavioral, and motor dysfunction. The clinical presentations or laboratory findings of treatable autoimmune and metabolic processes may mimic those of CJD. Hepatic encephalopathy (HE) is a complication of severe hepatic failure that is characterized by neuropsychiatric manifestations. A case of HE whose laboratory, physiological, and imaging results were similar to that of Creutzfeldt-Jakob disease (CJD) in the process of treatment for HE is presented. CASE REPORT: An 84-year-old woman with hepatic encephalopathy (HE) was admitted to our hospital because of acute consciousness disturbance. She had chronic hepatitis type C, liver cirrhosis, and hepatocellular carcinoma, and had had an episode of HE once. Her severe consciousness disturbance did not improve after treatment for concurrent hyperammonemia, unlike in her previous episode. Diffusion-weighted brain magnetic resonance imaging (MRI) showed widespread hyperintensity of the whole cortex. Her electroencephalogram showed periodic sharp wave complexes (PSWCs). Both total t-tau and 14-3-3 proteins were detected in her cerebrospinal fluid. According to these clinical data, CJD was highly suspected. However, the consciousness disturbance was alleviated by the tenth day of admission, and her general condition was markedly improved, which supported the initial diagnosis of HE. CONCLUSIONS: The present results suggest that treatable disorders, such as HE, should be considered before making a final diagnosis of a fatal disease such as CJD, since the spectrum of diseases that CJD mimics is vast. We should also aggressively treat patients with severe conditions from which recovery is possible. International Scientific Literature, Inc. 2021-08-22 /pmc/articles/PMC8392707/ /pubmed/34420027 http://dx.doi.org/10.12659/AJCR.932958 Text en © Am J Case Rep, 2021 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Articles Kimura, Masamune Kimura, Hideki Ishikawa, Hiroki Matsuo, Hisayasu Takada, Masahiko Matsuo, Koushun Hepatic Encephalopathy Mimicking Creutzfeldt-Jakob Disease on Laboratory, Physiological, and Imaging Evaluations |
title | Hepatic Encephalopathy Mimicking Creutzfeldt-Jakob Disease on Laboratory, Physiological, and Imaging Evaluations |
title_full | Hepatic Encephalopathy Mimicking Creutzfeldt-Jakob Disease on Laboratory, Physiological, and Imaging Evaluations |
title_fullStr | Hepatic Encephalopathy Mimicking Creutzfeldt-Jakob Disease on Laboratory, Physiological, and Imaging Evaluations |
title_full_unstemmed | Hepatic Encephalopathy Mimicking Creutzfeldt-Jakob Disease on Laboratory, Physiological, and Imaging Evaluations |
title_short | Hepatic Encephalopathy Mimicking Creutzfeldt-Jakob Disease on Laboratory, Physiological, and Imaging Evaluations |
title_sort | hepatic encephalopathy mimicking creutzfeldt-jakob disease on laboratory, physiological, and imaging evaluations |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8392707/ https://www.ncbi.nlm.nih.gov/pubmed/34420027 http://dx.doi.org/10.12659/AJCR.932958 |
work_keys_str_mv | AT kimuramasamune hepaticencephalopathymimickingcreutzfeldtjakobdiseaseonlaboratoryphysiologicalandimagingevaluations AT kimurahideki hepaticencephalopathymimickingcreutzfeldtjakobdiseaseonlaboratoryphysiologicalandimagingevaluations AT ishikawahiroki hepaticencephalopathymimickingcreutzfeldtjakobdiseaseonlaboratoryphysiologicalandimagingevaluations AT matsuohisayasu hepaticencephalopathymimickingcreutzfeldtjakobdiseaseonlaboratoryphysiologicalandimagingevaluations AT takadamasahiko hepaticencephalopathymimickingcreutzfeldtjakobdiseaseonlaboratoryphysiologicalandimagingevaluations AT matsuokoushun hepaticencephalopathymimickingcreutzfeldtjakobdiseaseonlaboratoryphysiologicalandimagingevaluations |