Polyneuropathies associated with plasma cell dyscrasias
著者
書誌事項
Polyneuropathies associated with plasma cell dyscrasias
（Topics in the neurosciences, TIN5）
Nijhoff, 1987 , Distributors for the United States and Canada, Kluwer Academic Publishers
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注記
Includes bibliographies and index
内容説明・目次
内容説明
Plasma cell dyscrasias are common causes of peripheral neuropathy. Peri- pheral neuropathy may be the first manifestation of multiple myeloma, amyloidosis, or monoclonal gammopathy of undetermined significance (MGUS). Peripheral neuropathy occurs in more than one-half of patients with osteosclerotic myeloma. The hematologic disorders are such an important association with peripheral polyneuropathy that, for the last decade, we have obtained a metastatic bone survey and immunoelectrophoresis of serum and a 24-hour urine specimen on all patients older than 40 years with undiagnosed peripheral neuropathy. This textbook on polyneuropathies and plasma cell dyscrasia is welcome, because the subject is of considerable medical importance and because the authors are expert in these disorders. Kelly's studies have shown that a systematic search for monoclonal proteins in plasma and urine among patients with neuropathy of unknown cause increases diagnostic yield. Latov's studies have focused on the role of myelin associated glycoproteins (MAG) in the induction of neuropathy.
Kyle, director of the Special Protein Laboratory at Mayo Clinic, brings a broad clinical and laboratory perspective and experi- ence. The timing of the textbook is just right, because there is much new information which needs to be summarized.
目次
1. Plasma cell dyscrasias: Definition and diagnostic evaluation.- 2. Epidemiology of polyneuropathies associated with plasma cell dyscrasias.- 3. Neurochemistry and neuroimmunology of peripheral nerve.- 4. Waldenstrom's macroglobulinemia and nonmalignant IgM monoclonal gammopathies.- 5. Nonmalignant IgG and IgA gammopathies.- 6. Multiple myeloma.- 7. Osteosclerotic myeloma.- 8. Amyloidosis.- 9. Diagnostic approach to patients with polyneuropathies associated with monoclonal proteins.- 10. Future directions.
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