A very rare cause of leukoencephalopathy: Lymphomatosis cerebri.

1H-MRS MRI Primary Central Nervous System lymphoma (PNCSL) leukoencephalopathy lymphomatosis cerebri

Journal

Intractable & rare diseases research
ISSN: 2186-3644
Titre abrégé: Intractable Rare Dis Res
Pays: Japan
ID NLM: 101586847

Informations de publication

Date de publication:
May 2023
Historique:
received: 25 12 2022
revised: 25 04 2023
accepted: 20 05 2023
medline: 8 6 2023
pubmed: 8 6 2023
entrez: 8 6 2023
Statut: ppublish

Résumé

Leukoencephalopathy is a common finding on Magnetic Resonance Imaging (MRI), particularly in the elderly. A differential diagnosis may represent a very bet for clinicians when clear elements for diagnosis are lacking. Diffuse infiltrative "non mass like" leukoencephalopathy on MRI may represent the presentation of a very rare aggressive condition known as lymphomatosis cerebri (LC). The lack of orienting data, such as contrast enhancement on MRI or specific findings on examination of Cerebrospinal Fluid (CSF) or blood tests, may even far more complicate such a difficult diagnosis and orientate toward a less aggressive but time-losing mimic. A 69-old man initially presented to the Emergency Department (ED) complaining the recent appearance of unsteady walking, limitation of down and upgaze palsy, and hypophonia. Brain MRI revealed the presence of multiple, confluent hyperintense lesions on T2/Flair Attenuated Imaging Recovery (FLAIR) sequences involving either the withe matter of the semi-oval centres, juxtacortical structures, basal ganglia, or bilateral dentate nuclei. DWI sequences showed a wide restriction signal in the same brain regions but without any sign of contrast enhancement. Initial 18F-labeled fluoro-2-deoxyglucose positron emission tomography (FDG PET) and CSF studies were not relevant. Brain MRI revealed a high choline-signal, abnormal Choline/ N-Acetyl-Aspartate (NAA), and Choline/Creatine (Cr) ratios, as well as reduced NAA levels. Finally, a brain biopsy revealed the presence of diffuse large B-cell lymphomatosis cerebri. The diagnosis of lymphomatosis cerebri remains elusive. The valorisation of brain imaging may induce clinicians to suspect such a difficult diagnosis and go through the diagnostic algorithm.

Identifiants

pubmed: 37287655
doi: 10.5582/irdr.2022.01134
pmc: PMC10242392
doi:

Types de publication

Journal Article

Langues

eng

Pagination

118-121

Informations de copyright

2023, International Research and Cooperation Association for Bio & Socio - Sciences Advancement.

Déclaration de conflit d'intérêts

The authors have no conflicts of interest to disclose.

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Auteurs

Maurizio Giorelli (M)

Operative Unit of Neurology, "Dimiccoli" General Hospital, Barletta, ASL BT, Italy.

Sergio Altomare (S)

Operative Unit of Neurology, "Dimiccoli" General Hospital, Barletta, ASL BT, Italy.

Maria Stella Aniello (MS)

Operative Unit of Neurology, "Dimiccoli" General Hospital, Barletta, ASL BT, Italy.

Maria Carmela Bruno (MC)

Operative Unit of Neurosurgery, "Bonomo" General Hospital, Andria, ASL BT, Italy.

Ruggiero Leone (R)

Operative Unit of Neurology, "Dimiccoli" General Hospital, Barletta, ASL BT, Italy.

Daniele Liuzzi (D)

Operative Unit of Neurology, "Dimiccoli" General Hospital, Barletta, ASL BT, Italy.

Giuseppe Ingravallo (G)

Institute of Pathologic Anatomy, Faculty of Medicine, University of Bari, Italy.

Pasquale Di Fazio (PD)

Operative Unit of Radiology, "Bonomo" General Hospital, Andria, ASL BT, Italy.

Tommaso Scarabino (T)

Operative Unit of Nuclear Medicine, "Dimiccoli" General Hospital, Barletta, ASL BT, Italy.

Giuseppe Tarantini (G)

Operative Unit of Ematology, "Dimiccoli" General Hospital, Barletta, ASL BT, Italy.

Classifications MeSH