Difference between revisions of "POEMS syndrome"

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'''POEMS syndrome''' is a constellation of findings:<ref name=pmid18477219>{{cite journal |author=Yuri T, Yamazaki F, Takasu K, Shikata N, Tsubura A |title=Glomeruloid hemangioma |journal=Pathol. Int. |volume=58 |issue=6 |pages=390–5 |year=2008 |month=June |pmid=18477219 |doi=10.1111/j.1440-1827.2008.02241.x |url=}}</ref>
'''POEMS syndrome''' is a constellation of findings, best thought of as a paraneoplastic syndrome due to clonal plasma cells:<ref name=pmid18477219>{{cite journal |author=Yuri T, Yamazaki F, Takasu K, Shikata N, Tsubura A |title=Glomeruloid hemangioma |journal=Pathol. Int. |volume=58 |issue=6 |pages=390–5 |year=2008 |month=June |pmid=18477219 |doi=10.1111/j.1440-1827.2008.02241.x |url=}}</ref>
*Polyneuropathy.  
*Polyneuropathy.  
*Organomegaly.
*Organomegaly.
Line 5: Line 5:
*M-protein.  
*M-protein.  
*Skin changes.
*Skin changes.
Diagnostic criteria requires both mandatory criteria and at least one each from major and minor criteria:<ref name=pmid31012139>{{cite journal |vauthors=Dispenzieri A |title=POEMS Syndrome: 2019 Update on diagnosis, risk-stratification, and management |journal=Am. J. Hematol. |volume=94 |issue=7 |pages=812–827 |date=July 2019 |pmid=31012139 |doi=10.1002/ajh.25495 |url=}}</ref>
''Mandatory:''
;1. Polyneuropathy (typically demyelinating)
;2. Monoclonal plasma cell proliferation (usually lambda)
''Major:''
;3. [[Castleman disease]]
;4. Sclerotic bone lesions
;5. Vascular endothelial growth factor elevation
''Minor:''
;6. Organomegaly (splenomegaly, hepatomegaly or lymphadenopathy)
;7. Extravascular volume overload
;8. Endocrinopathy
;9. Sking changes
;10. Papilloedema
;11. Thrombocytosis/polycythemia
POEMS syndrome is unusual in causing osteosclerotic bone deposits, so-called osteosclerotic myeloma, in contrast to the lytic lesions seen in more conventional [[plasma cell myeloma]].


==Pathology==
==Pathology==
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