Evidence map›Paper›PMID 40615985›Full record

ReviewBMC musculoskeletal disorders2025

Vacuolar myopathy associated with lambda light chain myeloma: a case report and review of the literature.

Quentin de Berny, Valéry Salle, Cédric Renard, Philippe-Edouard Merle, Nelly Guilain, Gabriel Choukroun, Pierre Morel, Ophélie Fourdinier

Abstract readCase ReportsReview
In one paragraph

Review in BMC musculoskeletal disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Quentin de BernyDepartment of Nephrology Dialysis Transplantation, Amiens University Hospital, 1 Rue du Professeur Christian Cabrol, Amiens, 80054, France. deberny.quentin@chu-amiens.fr.
Valéry SalleDepartment of Internal Medicine, Amiens University Hospital, Amiens, France.
Cédric RenardDepartment of Radiology, Amiens University Hospital, Amiens, France.
Philippe-Edouard MerleDepartment of Clinical Neurophysiology, Amiens University Hospital, Amiens, France.
Nelly GuilainDepartment of Pathology, Amiens University Hospital, Amiens, France.
Gabriel ChoukrounDepartment of Nephrology Dialysis Transplantation, Amiens University Hospital, 1 Rue du Professeur Christian Cabrol, Amiens, 80054, France.
Pierre MorelDepartment of Cellular Therapy and Haematology, Amiens University Hospital, Amiens, France.
Ophélie FourdinierDepartment of Nephrology Dialysis Transplantation, Amiens University Hospital, 1 Rue du Professeur Christian Cabrol, Amiens, 80054, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVacuolar myopathy is a muscle disease characterized by inefficient autophagy and the accumulation of intracytoplasmic degradation products in autophagic vacuoles. Acquired vacuolar myopathy associated with monoclonal gammopathy is a novel clinical entity first described in 2019. The objective of the present article is to describe the first case of an acquired vacuolar myopathy associated with lambda light chain myeloma. CASE PRESENTATION: A 52-year-old man was admitted to our nephrology department for acute kidney injury and was diagnosed with lambda light chain multiple myeloma. The patient presented with supraventricular arrythmia and developed rapidly progressing muscle weakness of the face and all four limbs, with a myogenic electromyographic pattern. A muscle biopsy highlighted muscle fibre vacuoles and lambda light chain deposits. Cardiac magnetic resonance imaging revealed concentric hypertrophy and subepicardial areas of fibrosis that were suggestive of an infiltrative disease. There were no signs of amyloidosis. Treatment with a combination of bortezomib, lenalidomide and dexamethasone gave a good hematologic response, and the patient recovered near-normal levels of muscle strength in the following six months. The number of episodes of arrythmia decreased.

conclusionClinicians should be aware that lambda light chain myeloma may cause lambda light-chain deposits within muscle fibres and vacuolar myopathy. A corticosteroid-sparing strategy for vacuolar myopathy does not appear to be necessary when the course of the myeloma is favourable. Myopathy associated with monoclonal gammopathy is an emerging entity. Given that monoclonal gammopathy is very common in older adults, the appearance of muscle impairments in this context could prompt the physician to consider the initiation of corticosteroids, immunosuppressive agents, or intravenous immunoglobulins. Electromyography and muscle biopsy results can guide the diagnosis.

Indexed as

Immunoglobulin lambda-ChainsLysosomal Storage DiseasesMultiple MyelomaMuscular DiseasesBortezomibDexamethasoneHumansLenalidomideMaleMiddle AgedMuscle, SkeletalBortezomibDexamethasoneImmunoglobulin lambda-ChainsLenalidomideCase reportLambda-light chainMonoclonal gammopathyMyelomaVacuolar myopathy

Identifiers

PMID40615985
PMCPMC12232129

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.