Acute psychosis following initiation of ruxolitinib in post-polycythaemia vera myelofibrosis case report

Polycythaemia vera (PV) is a myeloproliferative neoplasm (MPN) which can progress to myelofibrosis (MF), a phenomenon termed post-PV MF. Ruxolitinib is a Janus activated kinase (JAK) inhibitor that targets JAK1/2 mutations and is approved for treatment of high-risk MF. This is a case report of a patient with post-PV MF who developed acute psychotic disorder five months after commencing ruxolitinib and whose mental status returned to baseline within one week of stopping ruxolitinib. Importantly, there was no history of mental health disorder and no identifiable triggers for his presentation. Ruxolitinib has not previously been implicated in the development of psychosis but is known to cross the blood-brain barrier and affect multiple cell signalling pathways within the central nervous system. Together, this makes an association between ruxolitinib and neuropsychiatric symptoms plausible, yet further understanding of causal mechanisms is warranted.

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Publication Details

Journal
Annals of Hematology
Published
2026-01-22
DOI
https://doi.org/10.1007/s00277-026-06764-0
Primary Topic
Myeloproliferative Neoplasms: Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00
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article

Acute psychosis following initiation of ruxolitinib in post-polycythaemia vera myelofibrosis case report

Lucy Potter, Sachin Shetty, M Mansour Ceesay
Annals of Hematology
Myeloproliferative Neoplasms: Diagnosis and Treatment
article

Acute psychosis following initiation of ruxolitinib in post-polycythaemia vera myelofibrosis case report

Lucy Potter, Sachin Shetty, M Mansour Ceesay
article en

Abstract

Polycythaemia vera (PV) is a myeloproliferative neoplasm (MPN) which can progress to myelofibrosis (MF), a phenomenon termed post-PV MF. Ruxolitinib is a Janus activated kinase (JAK) inhibitor that targets JAK1/2 mutations and is approved for treatment of high-risk MF. This is a case report of a patient with post-PV MF who developed acute psychotic disorder five months after commencing ruxolitinib and whose mental status returned to baseline within one week of stopping ruxolitinib. Importantly, there was no history of mental health disorder and no identifiable triggers for his presentation. Ruxolitinib has not previously been implicated in the development of psychosis but is known to cross the blood-brain barrier and affect multiple cell signalling pathways within the central nervous system. Together, this makes an association between ruxolitinib and neuropsychiatric symptoms plausible, yet further understanding of causal mechanisms is warranted.

Annals of HematologyVol. 105(2)
King's College Hospital NHS Foundation Trust (GB), Kent and Medway NHS and Social Care Partnership Trust (GB)
Good health and well-being
Openalex Percentile: Top 79%
Myeloproliferative Neoplasms: Diagnosis and Treatment
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