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

**Authors:** Louise Jade Potter, Sachin Shetty, M. Mansour Ceesay

PMC · DOI: 10.1007/s00277-026-06764-0 · Annals of Hematology · 2026-01-23

## TL;DR

A patient with post-PV myelofibrosis developed acute psychosis after starting ruxolitinib, which resolved when the drug was stopped.

## Contribution

This case report links ruxolitinib to acute psychosis, suggesting a potential neuropsychiatric side effect.

## Key findings

- A patient developed acute psychosis five months after starting ruxolitinib.
- Psychosis resolved within a week of discontinuing ruxolitinib.
- No prior mental health history or identifiable triggers were present.

## 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.

The online version contains supplementary material available at 10.1007/s00277-026-06764-0.

## Linked entities

- **Chemicals:** ruxolitinib (PubChem CID 17754772)
- **Diseases:** myelofibrosis (MONDO:0044903)

## Full-text entities

- **Genes:** JAK3 (Janus kinase 3) [NCBI Gene 3718] {aka JAK-3, JAK3_HUMAN, JAKL, L-JAK, LJAK}, LGI1 (leucine rich glioma inactivated 1) [NCBI Gene 9211] {aka ADLTE, ADPAEF, ADPEAF, DEE121, EPITEMPIN, EPT}, EPO (erythropoietin) [NCBI Gene 2056] {aka DBAL, ECYT5, EP, MVCD2}, CNTNAP2 (contactin associated protein 2) [NCBI Gene 26047] {aka AUTS15, CASPR2, CDFE, NRXN4, PTHSL1}
- **Diseases:** hypoesthesia (MESH:D006987), dizziness (MESH:D004244), neurological adverse effects (MESH:D000069451), headache (MESH:D006261), neuropsychiatric effects (MESH:D065606), weakness (MESH:D018908), post (MESH:D000094025), psychosis (MESH:D011618), skin and nail hyperpigmentation (MESH:D017495), Acute psychosis (MESH:D011605), abdominal pain (MESH:D015746), pancytopenia (MESH:D010198), sleep disturbance (MESH:D012893), cognitive impairment (MESH:D003072), mania (MESH:D001714), agitation (MESH:D011595), PML (MESH:D007968), chronic myeloid leukaemia (MESH:D015451), MF (MESH:D055728), gait disturbance (MESH:D020233), diarrhoea (MESH:D003967), CNS (MESH:D002493), sickle cell trait (MESH:D012805), insomnia (MESH:D007319), acute psychotic syndrome (MESH:D000208), PV (MESH:D011087), neuropsychiatric (MESH:C000631768), osteosclerosis (MESH:D010026), neurodegenerative disorders (MESH:D019636), aggressive behaviour (MESH:D010554), excessive speech (MESH:D013064), neuropsychiatric symptoms (MESH:D001523), splenomegaly (MESH:D013163), mental health disorder (OMIM:603663), delusions (MESH:D063726), syphilis (MESH:D013587), neuroinflammation (MESH:D000090862), neutropenia (MESH:D009503), anaemia (MESH:D000743), ET (MESH:D013920), collagen fibrosis (MESH:D005355), MPN (MESH:D009369), auditory hallucinations (MESH:D006212), ulcerative colitis (MESH:D003093), dopaminergic dysfunction (MESH:D009422), thrombocytopenia (MESH:D013921), dysphasia (MESH:D001037), fatigue (MESH:D005221)
- **Chemicals:** tofacitinib (MESH:C479163), Ruxolitinib (MESH:C540383), Anagrelide (MESH:C021139), risperidone (MESH:D018967), JAK (-), HU (MESH:D006918)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus (species) [taxon 12721]
- **Mutations:** Cys1193Tyr, JAK2 V617F, V617F

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Source: https://tomesphere.com/paper/PMC12827360