# Progressive multifocal leukoencephalopathy as the initial manifestation of relapsed lymphoma: a case report

**Authors:** Shi Chen, Haitian Nan, Junjie Li

PMC · DOI: 10.3389/fonc.2026.1710057 · Frontiers in Oncology · 2026-02-18

## TL;DR

A young lymphoma patient developed progressive multifocal leukoencephalopathy (PML) as the first sign of cancer relapse, highlighting the importance of considering PML in immunocompromised patients with neurological symptoms.

## Contribution

This case report presents a rare instance where PML manifested before the initiation of new chemotherapy in a relapsed lymphoma patient.

## Key findings

- A 22-year-old male with a history of lymphoma developed neurological symptoms initially mistaken for CNS lymphoma relapse.
- Cerebrospinal fluid testing revealed a high JC polyomavirus (JCPyV) viral load, and brain biopsy confirmed PML.
- Chemotherapy worsened the patient's condition, emphasizing the need for PML suspicion in immunocompromised patients.

## Abstract

Progressive multifocal leukoencephalopathy (PML) is a rare and often fatal demyelinating disease of the central nervous system (CNS) caused by the reactivation of the JC polyomavirus (JCPyV). While PML is a known complication of hematological malignancies, it is exceedingly rare for it to manifest as the initial neurological symptom of a relapsed lymphoma, occurring even before the start of new systemic chemotherapy. We present a case of a 22-year-old male with a history of lymphoma who presented with progressive neurological deficits. The patient’s symptoms, including right-sided hemiparesis and aphasia, were initially mistaken for a CNS lymphoma relapse. Subsequent chemotherapy led to a rapid and severe clinical deterioration. Cerebrospinal fluid testing detected a high viral load of JCPyV. The patient underwent a brain biopsy, which revealed inflammatory changes consistent with the pathological changes of PML. This case highlights a critical diagnostic challenge and underscores the need for a high index of suspicion for PML in any immunocompromised patient with new-onset neurological symptoms, regardless of whether they have commenced new immunosuppressive therapy. It also serves as a poignant reminder of the potential for chemotherapy to exacerbate an underlying viral pathology.

## Linked entities

- **Diseases:** Progressive multifocal leukoencephalopathy (MONDO:0016318), lymphoma (MONDO:0003659)

## Full-text entities

- **Genes:** CD19 (CD19 molecule) [NCBI Gene 930] {aka B4, CVID3}, NFASC (neurofascin) [NCBI Gene 23114] {aka NEDCPMD, NF, NRCAML}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, PML (PML nuclear body scaffold) [NCBI Gene 5371] {aka MYL, PP8675, RNF71, TRIM19}
- **Diseases:** B-cell Lymphoma (MESH:D016393), lymphoproliferative disorders (MESH:D008232), AIDS (MESH:D000163), condition (MESH:D020763), CNS lymphoma (MESH:D008223), inflammation (MESH:D007249), speech deficits (MESH:D013064), PML (MESH:D007968), lymphadenopathy (MESH:D008206), chronic lymphocytic leukemia (MESH:D015451), non-Hodgkin lymphoma (MESH:D008228), right-hand tremor (MESH:D014202), cellular immunity deficiency (MESH:D007153), encephalopathy (MESH:D001927), demyelinated lesions (MESH:D003711), cancer (MESH:D009369), thrombocytopenia (MESH:D013921), B-cell deficiency (MESH:D015448), hematological malignancies (MESH:D019337), Inflammatory Flare (MESH:D000067251), fever (MESH:D005334), limb weakness (MESH:D018908), immune (MESH:D007154), seizure (MESH:D012640), infection (MESH:D007239), CNS infection (MESH:D002494), neurological deficits (MESH:D009461), HIV-infected (MESH:D015658), intracranial lesions (MESH:D020765), central nervous system (CNS) disorder (MESH:D002493), aphasia (MESH:D001037), osteolytic lesions (MESH:D030981), weight loss (MESH:D015431), CNS pathologies (MESH:D016543), scalp masses (MESH:C536030), CNS- Immune Reconstitution Inflammatory Syndrome (MESH:D054019), right-gaze deviation (MESH:D010262), hemiparesis (MESH:D010291)
- **Chemicals:** HE (MESH:D006371), LFB (MESH:C018588), R-GDP (-), Cisplatin (MESH:D002945), Hematoxylin (MESH:D006416), Rituximab (MESH:D000069283), GDP (MESH:D006153), pembrolizumab (MESH:C582435), Gemcitabine (MESH:D000093542), Dexamethasone (MESH:D003907), eosin (MESH:D004801), glucose (MESH:D005947), FDG (MESH:D019788)
- **Species:** Human immunodeficiency virus 1 (no rank) [taxon 11676], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376], Polyomavirus sp. (species) [taxon 36362], Homo sapiens (human, species) [taxon 9606], JC polyomavirus (no rank) [taxon 10632], SV40 [taxon 10633]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12956650/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12956650/full.md

## References

24 references — full list in the complete paper: https://tomesphere.com/paper/PMC12956650/full.md

---
Source: https://tomesphere.com/paper/PMC12956650