Neurolymphomatosis: involvement of peripheral nervous system revealing hematologic malignancy, a report of nine cases

Author:

Ducatel Pauline1ORCID,Michaud Maud1,Viala Karine2,Leblond Véronique3,Charlotte Frédéric4,Roos‐Weil Damien3,Benoit Charline2,Debs Rabab2,Maisonobe Thierry25

Affiliation:

1. Département de Neurologie Centre Hospitalier Régional Universitaire de Nancy Nancy France

2. Département de Neurophysiologie Clinique AP‐HP, Groupe Hospitalier Pitié‐Salpêtrière Paris France

3. Département d'Hématologie AP‐HP, Groupe Hospitalier Pitié‐Salpêtrière Paris France

4. Département d'Anatomopathologie AP‐HP, Groupe Hospitalier Pitié‐Salpêtrière Paris France

5. Département de Neuropathologie AP‐HP, Groupe Hospitalier Pitié‐Salpêtrière Paris France

Abstract

AbstractBackground and AimNeurolymphomatosis is defined as an infiltration of the peripheral nervous system (PNS) by malignant lymphoma cells. It is a rare entity and diagnosis is complicated especially when PNS involvement is the initial and leading symptom. To improve knowledge of the disorder and shorten the time to diagnosis, we report a series of nine patients without a history of hematologic malignancy, who were diagnosed with neurolymphomatosis after evaluation and workup of peripheral neuropathy.MethodsThe patients were included from the Department of Clinical Neurophysiology at Pitié Salpêtrière and Nancy Hospitals over a period of 15 years. Diagnosis of neurolymphomatosis was confirmed by histopathologic examination for each patient. We characterized their clinical, electrophysiological, biological, imaging, and histopathologic features.ResultsThe neuropathy was characterized by pain (78%), proximal involvement (44%) or of all four limbs (67%), asymmetrical or with multifocal distribution (78%), abundant fibrillation (78%), a tendency to worsen rapidly, and significant associated weight loss (67%). Neurolymphomatosis was diagnosed principally on nerve biopsy (89%) identifying infiltration of lymphoid cells, atypical cells (78%), a monoclonal population (78%), and supported by fluorodeoxyglucose‐positron emission tomography, spine or plexus MRI, cerebrospinal fluid analysis, and blood lymphocyte immunophenotyping. Six patients had systemic disease and three impairment limited to the PNS. In the latter case, progression could be unpredictable and may be diffuse and explosive, sometimes occurring years after a seemingly indolent course.InterpretationThis study provides better knowledge and understanding of neurolymphomatosis when neuropathy is the initial presentation.

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

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