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Hyperammonemic Encephalopathy: A Rare Presentation of Relapsed Multiple Myeloma

Hyperammonemia is a rare cause of encephalopathy in multiple myeloma in the absence of hepatic involvement. This is the only reported case of a 74-year-old man who presented with multiple myeloma and achieved complete remission but developed hyperammonemia afterward. He was aggressively treated with...

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Autores principales: Menakuru, Sasmith R., Atta, Mona, Ammannagari, Nischala, Younes, Mohamad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10332859/
https://www.ncbi.nlm.nih.gov/pubmed/37435418
http://dx.doi.org/10.14740/jh1097
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author Menakuru, Sasmith R.
Atta, Mona
Ammannagari, Nischala
Younes, Mohamad
author_facet Menakuru, Sasmith R.
Atta, Mona
Ammannagari, Nischala
Younes, Mohamad
author_sort Menakuru, Sasmith R.
collection PubMed
description Hyperammonemia is a rare cause of encephalopathy in multiple myeloma in the absence of hepatic involvement. This is the only reported case of a 74-year-old man who presented with multiple myeloma and achieved complete remission but developed hyperammonemia afterward. He was aggressively treated with a combination of chemotherapy and immunotherapy, with a resolution of his encephalopathy; however, within one month, he relapsed with encephalopathy. He ultimately decided to pursue comfort-care measures. The authors conclude that hyperammonemia in multiple myeloma is a rare but important differential in patients with encephalopathy of unknown causes. Aggressive treatment is of the utmost importance due to the high mortality associated with the condition.
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spelling pubmed-103328592023-07-11 Hyperammonemic Encephalopathy: A Rare Presentation of Relapsed Multiple Myeloma Menakuru, Sasmith R. Atta, Mona Ammannagari, Nischala Younes, Mohamad J Hematol Case Report Hyperammonemia is a rare cause of encephalopathy in multiple myeloma in the absence of hepatic involvement. This is the only reported case of a 74-year-old man who presented with multiple myeloma and achieved complete remission but developed hyperammonemia afterward. He was aggressively treated with a combination of chemotherapy and immunotherapy, with a resolution of his encephalopathy; however, within one month, he relapsed with encephalopathy. He ultimately decided to pursue comfort-care measures. The authors conclude that hyperammonemia in multiple myeloma is a rare but important differential in patients with encephalopathy of unknown causes. Aggressive treatment is of the utmost importance due to the high mortality associated with the condition. Elmer Press 2023-06 2023-04-30 /pmc/articles/PMC10332859/ /pubmed/37435418 http://dx.doi.org/10.14740/jh1097 Text en Copyright 2023, Menakuru et al. https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Menakuru, Sasmith R.
Atta, Mona
Ammannagari, Nischala
Younes, Mohamad
Hyperammonemic Encephalopathy: A Rare Presentation of Relapsed Multiple Myeloma
title Hyperammonemic Encephalopathy: A Rare Presentation of Relapsed Multiple Myeloma
title_full Hyperammonemic Encephalopathy: A Rare Presentation of Relapsed Multiple Myeloma
title_fullStr Hyperammonemic Encephalopathy: A Rare Presentation of Relapsed Multiple Myeloma
title_full_unstemmed Hyperammonemic Encephalopathy: A Rare Presentation of Relapsed Multiple Myeloma
title_short Hyperammonemic Encephalopathy: A Rare Presentation of Relapsed Multiple Myeloma
title_sort hyperammonemic encephalopathy: a rare presentation of relapsed multiple myeloma
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10332859/
https://www.ncbi.nlm.nih.gov/pubmed/37435418
http://dx.doi.org/10.14740/jh1097
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