POEMS Syndrome: Latest Comprehensive Review
Keywords:
POEMS syndrome, polyneuropathy, organomegaly, endocrinopathiesAbstract
Background: POEMS syndrome includes polyneuropathy, organomegaly, endocrinopathies, M protein, and skin changes. POEMS syndrome is a rare disorder with a mean age of onset between 46 and 56 years. Progressive POEMS syndrome can cause severe cardiorespiratory compromise, in some patients resulting in premature death. Early and aggressive diagnosis and treatment is required. Purpose: there are not many recent reviews describing POEMS syndrome, so the author wants to bring together various related literature and provide the latest references regarding POEMS syndrome. Method: Various related literature was retrieved over a period of 3 (three) years using the Google Scholar database, PubMed, Cochrane Library with the keyword "POEMS Syndrome". The analysis and arrangement of the study was carried out after fulfilling the inclusion and exclusion criteria. Results: POEMS syndrome is a rare paraneoplastic syndrome due to an underlying plasma cell abnormality. Neuropathy which is the main characteristic and important criterion for diagnosis. The POEMS Syndrome Diagnostic Criteria can be used to help establish the diagnosis. Conclusion: The right diagnosis can provide appropriate management so that good long-term clinical results are obtained.
Downloads
Published
How to Cite
Issue
Section
Citation Check
License
Copyright (c) 2023 Vira Teresia, Ririn, Clara Alvionita Wongso, Vira Geraldine Arliska, Lisa Setio (Author)
This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.
Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution-ShareAlike 4.0 International License that allows others to share the work with an acknowledgment of the works authorship and initial publication in this journal and able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journals published version of the work (e.g., post it to an institutional repository or publish it in a book).