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Wien Klin Wochenschr. 1976 Apr 30;88(9):281-5.

[The diagnosis of IgD-Myelomatosis (author's transl)].

[Article in German]


Two patients with IgD-lambda myelomatosis are presented and the differential diagnosis is discussed. Typical features of this disease are the high incidence of Bence-Jones proteinuria, osteolytic lesions, amyloidosis and the predominance of male patients. Furthermore, an augmentation of serum IgD level to 165 mg% was observed in a 22-year-old female patient with presumed Coxsackie myocarditis. The theories in regard to IgD function are discussed.

[Indexed for MEDLINE]

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