POEMS syndrome

POEMS syndrome is a paraneoplastic syndrome characterized by polyradiculoneuropathy (P), organomegaly (O), endocrinopathy (E), clonal plasma cell disorder (M), and skin changes (S). Other features include papilledema, extravascular volume overload, sclerotic bone lesions, thrombocytosis/erythrocytosis, and elevated VEGF levels.

Myelopathy



Total: 3

                       


(per page)
PMID (PMCID)
15273889
 FEMALE
[Paraparesis, hyperprolactinemia and adynamic ileus in Guillain-Barre syndrome].
Gazulla Abio J, Benavente Aguilar I.
Neurologia. 2004;19(7):396-400.
Differential diagnosis with myelopathy, metabolic and paraneoplasic neuropathies, POEMS syndrome, chronic inflammatory demyelinating polyneuropathy and recurrent Guillain-Barre syndrome are commented on.
8334776
 MALE Adult
[A case of Crow-Fukase syndrome which developed seven years following myelopathy of unknown origin].
Furuzono H, Moritoyo T, Yamada H, Sugihara R, Nagamatsu K.
Rinsho Shinkeigaku. 1993;33(1):56-60.
A rare case of Crow-Fukase syndrome was reported, which developed 7 years following myelopathy of unknown origin.
8334776
 MALE Adult
[A case of Crow-Fukase syndrome which developed seven years following myelopathy of unknown origin].
Furuzono H, Moritoyo T, Yamada H, Sugihara R, Nagamatsu K.
Rinsho Shinkeigaku. 1993;33(1):56-60.
[A case of Crow-Fukase syndrome which developed seven years following myelopathy of unknown origin].