Hyperammonemic Encephalopathy: A Rare Presentation of Relapsed Multiple Myeloma

dc.contributor.authorMenakuru, Sasmith R.
dc.contributor.authorAtta, Mona
dc.contributor.authorAmmannagari, Nischala
dc.contributor.authorYounes, Mohamad
dc.contributor.departmentMedicine, School of Medicine
dc.date.accessioned2024-02-13T10:08:29Z
dc.date.available2024-02-13T10:08:29Z
dc.date.issued2023
dc.description.abstractHyperammonemia 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.
dc.eprint.versionFinal published version
dc.identifier.citationMenakuru SR, Atta M, Ammannagari N, Younes M. Hyperammonemic Encephalopathy: A Rare Presentation of Relapsed Multiple Myeloma. J Hematol. 2023;12(3):128-132. doi:10.14740/jh1097
dc.identifier.urihttps://hdl.handle.net/1805/38413
dc.language.isoen_US
dc.publisherElmer Press
dc.relation.isversionof10.14740/jh1097
dc.relation.journalJournal of Hematology
dc.rightsAttribution-NonCommercial 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.sourcePMC
dc.subjectHyperammonemia
dc.subjectEncephalopathy
dc.subjectMultiple myeloma
dc.subjectTreatment
dc.titleHyperammonemic Encephalopathy: A Rare Presentation of Relapsed Multiple Myeloma
dc.typeArticle
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