KMID : 1044320230250020084
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Annals of Clinical Neurophysiology 2023 Volume.25 No. 2 p.84 ~ p.92
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Electrophysiological features and prognosis of peripheral neuropathy associated with IgM monoclonal gammopathy: a single-center analysis in South Korea
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Kim Soo-Young
Lee Bit-Na Kim Seung-Woo Shin Ha-Young
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Abstract
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Background : Clinical spectrum of immunoglobulin M (IgM) monoclonal gammopathy varies from IgM monoclonal gammopathy of unknown significance (IgM-MGUS) to hematological malignancies. We evaluated the clinical features, electrophysiological characteristics, and prognosis of patients with peripheral neuropathy associated with IgM monoclonal gammopathy (PN-IgM MG).
Methods : We retrospectively evaluated 25 patients with PN-IgM MG. Peripheral neuropathy was classified as axonal, demyelinating, or undetermined, based on electrophysiological studies. We classified the enrolled patients into the IgM-MGUS and malignancy groups, and compared the clinical and electrophysiological features between the groups.
Results : Fifteen patients had IgM-MGUS and 10 had hematologic malignancies (Waldenstrom¡¯s macroglobulinemia: two and B-cell non-Hodgkin¡¯s lymphoma: eight). In the electrophysiological evaluation, the nerve conduction study (NCS) criteria for demyelination were met in 86.7% of the IgM-MGUS group and 10.0% of the malignancy group. In particular, the distal latencies of the motor NCS in the IgM-MGUS group were significantly prolonged compared to those in the malignancy group (median, 9.1 ¡¾ 5.1 [IgM-MGUS], 4.2 ¡¾ 1.3 [malignancy], p = 0.003; ulnar, 5.4 ¡¾ 1.9 [IgM-MGUS], 2.9 ¡¾ 0.9 [malignancy], p = 0.001; fibular, 9.3 ¡¾ 5.1 [IgM-MGUS], 3.8 ¡¾ 0.3 [malignancy], p = 0.01; P-posterior tibial, 8.3 ¡¾ 5.4 [IgM-MGUS], 4.4 ¡¾ 1.0 [malignancy], p = 0.04). Overall treatment responses were significantly worse in the malignancy group than in the IgM-MGUS group (p = 0.004), and the modified Rankin Scale score at the last visit was higher in the malignancy group than in the IgM-MGUS group (2.0 ¡¾ 1.1 [IgM-MGUS], 4.2 ¡¾ 1.7 [malignancy], p = 0.001), although there was no significant difference at the initial assessment.
Conclusions : The risk of hematological malignancy should be carefully assessed in patients with PN-IgM MG without electrophysiological demyelination features.
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KEYWORD
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Paraproteinemia, Monoclonal gammopathy of undetermined significance, Hematologic neoplasms, Peripheral nervous system diseases, Nerve conduction studies
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