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A case of POEMS syndrome treated by autologous hematopoietic stem-cell transplantation

Abstract

Background A 55-year-old woman with no remarkable medical history presented to a neurology ward with a 17-week history of rapidly progressive gait difficulties that confined her to a wheelchair.

Investigations Electroneuromyography, immunoelectrophoresis, bone radiography, lesion-targeted bone-marrow examination, blood tests.

Diagnosis Neuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome.

Management High-dose chemotherapy and autologous hematopoietic stem-cell transplantation.

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Figure 1: CT scan of the pelvis of a patient with POEMS syndrome.

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Acknowledgements

We would like to thank Janet Jacobson for her excellent editorial assistance. Désirée Lie, University of California, Irvine, CA, is the author of and is solely responsible for the content of the learning objectives, questions and answers of the Medscape-accredited continuing medical education activity associated with this article

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Correspondence to Alain Créange.

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The authors declare no competing financial interests.

Supplementary information

Supplementary Table 1

Electrophysiological changes consistent with a severe demyelinating polyneuropathy in the present patient (DOC 106 kb)

Supplementary Table 2

Biological parameters in the present patient (DOC 59 kb)

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Créange, A., Chater, A., Brouet, JC. et al. A case of POEMS syndrome treated by autologous hematopoietic stem-cell transplantation. Nat Rev Neurol 4, 686–691 (2008). https://doi.org/10.1038/ncpneuro0942

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