Myeloma‐Associated Sporadic Late‐Onset Nemaline Myopathy, Successfully Treated with Daratumumab Based Induction and Autologous Stem Cell Transplantation: A Case Report

ABSTRACT Sporadic late‐onset nemaline myopathy (SLONM) is a rare, acquired myopathy often associated with monoclonal gammopathy. We report a 48‐year‐old man presenting with progressive proximal and truncal muscle weakness in whom SLONM associated with smoldering myeloma was highly suspected. He received daratumumab, lenalidomide, and dexamethasone followed by high‐dose melphalan with autologous stem cell transplantation and posttransplant therapy. Treatment resulted in marked improvement in muscle strength and performance status. The patient achieved minimal residual disease negativity and has remained relapse‐free for 5 years. This case highlights the potential efficacy of daratumumab‐based therapy followed by transplantation in SLONM associated with plasma cell dyscrasia. Trial Registration: The authors have confirmed clinical trial registration is not needed for this submission.

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Publication Details

Journal
eJHaem
Published
2026-09-15
DOI
https://doi.org/10.1002/jha2.70390
Primary Topic
Cardiomyopathy and Myosin Studies
Type
article
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Myeloma‐Associated Sporadic Late‐Onset Nemaline Myopathy, Successfully Treated with Daratumumab Based Induction and Autologous Stem Cell Transplantation: A Case Report

Jun‐ichirou Yasunaga, Mitsuharu Ueda, Yawara Kawano, Makoto Nakajima et al.
eJHaem
Cardiomyopathy and Myosin Studies
article

Myeloma‐Associated Sporadic Late‐Onset Nemaline Myopathy, Successfully Treated with Daratumumab Based Induction and Autologous Stem Cell Transplantation: A Case Report

Jun‐ichirou Yasunaga, Mitsuharu Ueda, Yawara Kawano, Makoto Nakajima, Nao Nishimura, Kenji Moriwaki
article en

Abstract

ABSTRACT Sporadic late‐onset nemaline myopathy (SLONM) is a rare, acquired myopathy often associated with monoclonal gammopathy. We report a 48‐year‐old man presenting with progressive proximal and truncal muscle weakness in whom SLONM associated with smoldering myeloma was highly suspected. He received daratumumab, lenalidomide, and dexamethasone followed by high‐dose melphalan with autologous stem cell transplantation and posttransplant therapy. Treatment resulted in marked improvement in muscle strength and performance status. The patient achieved minimal residual disease negativity and has remained relapse‐free for 5 years. This case highlights the potential efficacy of daratumumab‐based therapy followed by transplantation in SLONM associated with plasma cell dyscrasia. Trial Registration: The authors have confirmed clinical trial registration is not needed for this submission.

eJHaemVol. 7(5)
Kumamoto University (JP)
Good health and well-being
Openalex Percentile: Top 11%
Cardiomyopathy and Myosin Studies
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