POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes) syndrome is a rare multisystem disorder associated with osteosclerotic myeloma. It is characterized by peripheral polyneuropathy, presence of monoclonal plasma cell proliferative disorder, and one or more of the following features – sclerotic bone lesions, Castleman disease, elevated levels of vascular endothelial growth factor, organomegaly, extravascular volume overload, endocrinopathy, skin changes, papilledema, and thrombocytosis. Extramedullary plasmacytoma (EMP) is a rare plasma cell neoplasm that arises in isolated tissues without bone marrow involvement or systemic characteristics of multiple myeloma. Herein, we report a male patient who was previously diagnosed with EMP and later developed POEMS.

Paraproteinemia is caused by a proliferation of monoclonal plasma cells or B lymphocytes. Approximately 10% of idiopathic neuropathies are associated with paraproteinemia, where a certain paraprotein acts like an antibody targeted at constituents of myelin or axolemma in peripheral nerves. The relationship between paraproteinemia and peripheral neuropathy remains unclear despite this being of interest for a long time. Neurologists frequently find paraproteinemia during laboratory examinations of patients presenting with peripheral neuropathy, especially in the elderly. The possibility of a relationship with paraproteinemia should be considered in cases without an explainable cause. We review the causal association between paraproteinemia and neuropathy as well as clinical, laboratory, and electrophysiologic features, and the treatment options for paraproteinemic neuropathy.

Citations

• A Practical Review of Paraproteinemic Neuropathy
  Joong-Yang Cho
  Korean Journal of Neuromuscular Disorders.2022; 14(2): 23.     CrossRef

POEMS syndrome is a multisystem disorder associated with polyneuropathy, organomegaly, endocrinopathy, a monoclonalprotein(M-protein), and skin change. Recently we have had the opportunity to attend one patient with clinicalfeatures similar to this syndrome. He was a 46-year-old man who had a progressive polyneuropathy, swallowing difficulty,hepatosplenomegaly, hypothyroidism, IgA

Background
s and objectives: POEMS (polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes)syndrome is the rare cause of polyneuropathy. Although the polyneuropathy is essential for the diagnosis of the disease,the pattern of electrodiagnostic abnormalities has not been characterized in detail. The purpose of this study was to elucidatethe features of nerve conduction abnormalities in POEMS syndrome. Methods: We reviewed the medical recordsand nerve conduction studies (NCS) of 12 consecutive patients with POEMS. Results: A total of 68 motor and 46 sensorynerves were examined. Compound muscle action potentials (CMAPs) and sensory nerve action potentials wereabnormally attenuated or not elicited in majority of motor and sensory nerves (80.88% in motor, and 82.6% in sensorynerves). Frequency of the nerves with no potential was significantly higher in lower limbs than in upper limbs (p<0.01in both motor and sensory nerves), and CMAP amplitude was more reduced in lower limbs than in upper limbs(p<0.01). Conduction slowing was very frequently observed with 95% and 76% of motor and sensory nerves, respectively,having the abnormally reduced values of conduction velocity. Distal motor latencies were abnormally prolongedin 75% of motor nerves, and terminal latency indices were significantly higher in patients than in normal controls (p <0.05). Conduction block was observed only in 5% of motor nerves. Conclusions: NCS in POEMS syndrome showedcharacteristic patterns, in which conduction abnormalities were more frequently and severely affected in the lowerlimbs, and more predominantly in the intermediate nerve segments than in the distal portions. The recognition of thesecharacteristic patterns may be helpful in early diagnosis of polyneuropathy in POEMS syndrome.