Abstract
Abstract Peripheral neuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes are often the presenting features of the POEMS syndrome. Approximately 50% of these are associated with osteosclerotic myeloma, a rare variant of multiple myeloma and some with Castlemanapos;s disease, an unusual lympho‐proliferative disorder. The underlying pathogenetic mechanisms have not been elucidated but amelioration of symptoms with the disappearance of the M‐component suggests possible etiopathogenic mechanisms. We present a 40‐year‐old woman with manifestations of all three disorders. (Aust NZ J Med 1991; 21:454–456.).
Original language | English |
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Pages (from-to) | 454-456 |
Number of pages | 3 |
Journal | Australian and New Zealand Journal of Medicine |
Volume | 21 |
Issue number | 4 |
DOIs | |
Publication status | Published - Aug 1991 |
Externally published | Yes |
Keywords
- Castleman's disease
- osteosclerotic myeloma
- POEMS syndrome