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A Case of POEMS Syndrome Previously Diagnosed with Extramedullary Plasmacytoma / 대한신경근육질환학회지
Korean Journal of Neuromuscular Disorders ; (2): 59-63, 2021.
Article in Korean | WPRIM | ID: wpr-917946
ABSTRACT
POEMS (polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin changes) syndrome is a rare multisystem disorder associated with osteosclerotic myeloma. It is characterized by peripheral polyneuropathy, presence of monoclonal plasma cell proliferative disorder, and one or more of the following features – sclerotic bone lesions, Castleman disease, elevated levels of vascular endothelial growth factor, organomegaly, extravascular volume overload, endocrinopathy, skin changes, papilledema, and thrombocytosis. Extramedullary plasmacytoma (EMP) is a rare plasma cell neoplasm that arises in isolated tissues without bone marrow involvement or systemic characteristics of multiple myeloma. Herein, we report a male patient who was previously diagnosed with EMP and later developed POEMS.
Full text: Available Index: WPRIM (Western Pacific) Type of study: Diagnostic study Language: Korean Journal: Korean Journal of Neuromuscular Disorders Year: 2021 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Type of study: Diagnostic study Language: Korean Journal: Korean Journal of Neuromuscular Disorders Year: 2021 Type: Article