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An Atypical Case of POEMS Syndrome with an Osteolytic Bone Lesion
Kumar Rahul1, Nayha Handa1, S H Chandrashekhara2
1Senior Resident, Department of Radiology, AIIMS , New Delhi, India .
Abstract:
POEMS syndrome is a rare multisystem disorder with an underlying plasma cell dyscrasia associated with Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal gammopathy and Skin changes. Usually it is associated with sclerotic bone lesions. It usually manifests in 5(th)-6(th) decade of life with a mean survival period of eight years. We report an unusual case of a 28-year-old male diagnosed with POEMS syndrome and had a lytic bone lesion the in sternum.
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