The diagnosis of POEMS (polyneuropathy, organomegaly, endocrinopathy, M protein, skin
changes) syndrome is made based on a composite of clinical and laboratory features (Table …

Importance POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal
gammopathy, and skin changes) syndrome is a rare plasma cell disorder characterized by …

POEMS syndrome is a unique clinical entity. Although it's a diagnosis of exclusion, it was
previously described by the presence of several typical characteristics as paraproteinemia …

The POEMS syndrome (coined to refer to polyneuropathy, organomegaly, endocrinopathy,
M protein, and skin changes) remains poorly understood. Ambiguity exists over the features …

Polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes
(POEMS) syndrome is a rare condition defined by monoclonal plasma cell disorder …

The POEMS syndrome, also known as Crow-Fukase disease, is a rare multisystem disorder,
which may take several years to evolve fully. The combination of symptoms and signs is …

POEMS syndrome is a rare disorder characterized by polyneuropathy, monoclonal
gammopathy, multiorgan involvement, and elevated vascular endothelial growth factor …

Disease overview: POEMS syndrome is a paraneoplastic syndrome due to an underlying
plasma cell neoplasm. The major criteria for the syndrome are polyradiculoneuropathy …

POEMS syndrome is a rare plasma cell disorder characterized by polyneuropathy,
organomegaly, endocrinopathy, M-protein, and skin changes associated with multiorgan …

Objective: POEMS syndrome with its classical five findings (Polyneuropathy, Organomegaly,
Endocrinopathy, M protein, and Skin changes) is a rare multisystem disease …