An Atypical Case of POEMS Syndrome with an Osteolytic Bone Lesion
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...
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Published in: | Journal of clinical and diagnostic research Vol. 9; no. 6; pp. XD01 - XD02 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
India
JCDR Research and Publications (P) Limited
01-06-2015
JCDR Research and Publications Private Limited |
Subjects: | |
Online Access: | Get full text |
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Summary: | 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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ISSN: | 2249-782X 0973-709X |
DOI: | 10.7860/JCDR/2015/12998.6099 |