1. POEMS syndrome: studies in a patient with an IgG-kappa M protein but no polyneuropathy
- Author
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David P. Huston, Saul W. Rosen, Ernst J. Schaefer, and Jay S. Morrow
- Subjects
Galactorrhea ,medicine.medical_specialty ,Pathology ,medicine.medical_treatment ,Immunoglobulins ,Endocrine System Diseases ,Gastroenterology ,Skin Diseases ,Thyroiditis ,Organomegaly ,Immunoglobulin kappa-Chains ,Polyneuropathies ,Internal medicine ,Hypergammaglobulinemia ,Biopsy ,Internal Medicine ,medicine ,Humans ,POEMS syndrome ,medicine.diagnostic_test ,business.industry ,Biopsy, Needle ,Blood Proteins ,Plasmapheresis ,Syndrome ,Middle Aged ,medicine.disease ,Hyperpigmentation ,Thyroid Diseases ,Immunoglobulin G ,Splenomegaly ,Female ,Immunoglobulin Light Chains ,medicine.symptom ,business ,Polyneuropathy ,Pigmentation Disorders - Abstract
• A 48-year-old woman had a variation of the syndrome of polyneuropathy, organomegaly, endocrinopathy,Mprotein, and skin changes (the so-called POEMS syndrome). The patient's neurological findings were entirely normal, but she had splenomegaly, hyperprolactinemia with galactorrhea and oligomenorrhea, a thyroid nodule with evidence of mild thyroiditis on aspiration biopsy specimen, an IgG-κ monoclonal gammopathy, and hyperpigmentation and thickening of the skin. A short course of plasmapheresis (twelve 4-L exchanges in one month) did not alter any of the clinical abnormalities, but did result in a 70% decrease in the monoclonal IgG level (from 2.2 to 0.7 g/dL). (Arch Intern Med1982;142:1231-1234)
- Published
- 1982