POEMS syndrome--a case for more aggressive treatment

Patients with POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal or M-protein and skin changes) syndrome exhibit a wide range of clinical manifestations and are often seen by a variety of specialists prior to diagnosis. We describe a case of POEMS syndrome that first presented with sign...

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Bibliographic Details
Published inAnnals of the Academy of Medicine, Singapore Vol. 36; no. 6; pp. 435 - 437
Main Authors Rathakrishnan, Rahul, Liu, Te-Chih, Chan, Yee-Cheun, Ong, Benjamin K C
Format Journal Article
LanguageEnglish
Published Singapore 01.06.2007
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Summary:Patients with POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal or M-protein and skin changes) syndrome exhibit a wide range of clinical manifestations and are often seen by a variety of specialists prior to diagnosis. We describe a case of POEMS syndrome that first presented with significant neuropathy but progressed to develop further manifestations of the condition, including marked gastrointestinal symptoms. The patient was commenced on localised radiotherapy and chemotherapy in addition to immunomodulatory therapy for the neuropathy. We highlight several learning points that may benefit physicians from varied specialties. This case is also unique for its marked gastrointestinal manifestation. To our knowledge, this is the second reported case in the literature with this feature.
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ISSN:0304-4602
0304-4602
DOI:10.47102/annals-acadmedsg.V36N6p435