Creutzfeldt-Jakob disease - Case report

Presenter Information

Arieta Hasani Alidema
Melihate Pushka

Session

Medicine and Nursing

Description

Jakob-Creutzfeldt disease is a degenerative disorder that causes dementia and eventually death. It is usually diagnosed in the advanced stages because it gives a variety of atypical symptoms until the final stages. This case presentation aims to reflect the case of a woman with pronounced cognitive and psychiatric symptoms and her diagnostic journey until shortly before her death.

Case report: The 63-year-old patient had gradually started with subtle psychic changes, in the form of paranoid ideas, anxiety, a state of generally depressed mood, and changes in personality. Gradually the changes became more pronounced and in the last two weeks before hospitalization, she changed completely, slowing down and manifesting a state of psychomotor disturbance with visual hallucinations. After wandering through several clinics of the UCCK, she is hospitalized at the Neurological Department, where a lumbar puncture, MRI of the brain, and EEG are performed. The final diagnosis was made after the arrival of the results, i.e. imaging changes in the nucleus lentiform, nucleus caudatus, and bilateral corona radiata; specific sharp triphasic waves in the EEG and finally the identification of the 14-3-3 protein in the cerebrospinal fluid.

Conclusion: CJDdisease is rare, but it should be considered in the differential diagnosis as we often have patients with progressive cognitive and psychic changes, along with symptoms such as myoclonus and visual hallucinations.

Keywords:

Creutzfeldt-Jakob disease, cognitive decline, psychic changes, neurodegenerative disorder.

Proceedings Editor

Edmond Hajrizi

ISBN

978-9951-550-50-5

Location

UBT Kampus, Lipjan

Start Date

29-10-2022 12:00 AM

End Date

30-10-2022 12:00 AM

DOI

10.33107/ubt-ic.2022.186

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Creutzfeldt-Jakob disease - Case report

UBT Kampus, Lipjan

Jakob-Creutzfeldt disease is a degenerative disorder that causes dementia and eventually death. It is usually diagnosed in the advanced stages because it gives a variety of atypical symptoms until the final stages. This case presentation aims to reflect the case of a woman with pronounced cognitive and psychiatric symptoms and her diagnostic journey until shortly before her death.

Case report: The 63-year-old patient had gradually started with subtle psychic changes, in the form of paranoid ideas, anxiety, a state of generally depressed mood, and changes in personality. Gradually the changes became more pronounced and in the last two weeks before hospitalization, she changed completely, slowing down and manifesting a state of psychomotor disturbance with visual hallucinations. After wandering through several clinics of the UCCK, she is hospitalized at the Neurological Department, where a lumbar puncture, MRI of the brain, and EEG are performed. The final diagnosis was made after the arrival of the results, i.e. imaging changes in the nucleus lentiform, nucleus caudatus, and bilateral corona radiata; specific sharp triphasic waves in the EEG and finally the identification of the 14-3-3 protein in the cerebrospinal fluid.

Conclusion: CJDdisease is rare, but it should be considered in the differential diagnosis as we often have patients with progressive cognitive and psychic changes, along with symptoms such as myoclonus and visual hallucinations.