Korean J Hematol 2008; 43(4):
Published online December 31, 2008
https://doi.org/10.5045/kjh.2008.43.4.253
© The Korean Society of Hematology
양재훈 정주영 소찬수 임유진 한승용 박사라 김정한 허미나 이경규 심정원 박영이
한강성심병원 방사선과,내과,병리학과
국립의료원 내과
POEMS syndrome is a plasma cell proliferative disorder is characterized by the presence of peripheral neuropathy (P), organomegaly (O), monoclonal gammopathy (M), endocrinopathy or edema (E) and skin change (S). It can be rarely related to multiple myeloma. A 48-year-old man was admitted to our hospital due to paresthesia of both inguinal areas and weakness of both lower extremities. He had a history of Castleman's disease, and showed features of polyneuropathy, multiple osteoblastic lesions, hepatosplenomegaly, pretibial pitting edema, and papilledema. The serum and urine electrophoresis were negative, but urine immunofixagion could detect monoclonal protein. Plasmacytoma was confirmed through the biopsy for the osteoblastic lesions. We present a case of combined POEMS syndrome and multiple myeloma with positive M protein only on immunofixation in order to share our experience with physicians and specialists. (Korean J Hematol 2008;43:253-257.)
Keywords POEMS syndrome, Multiple myeloma, Osteoblastic lesion
Korean J Hematol 2008; 43(4): 253-257
Published online December 31, 2008 https://doi.org/10.5045/kjh.2008.43.4.253
Copyright © The Korean Society of Hematology.
양재훈 정주영 소찬수 임유진 한승용 박사라 김정한 허미나 이경규 심정원 박영이
한강성심병원 방사선과,내과,병리학과
국립의료원 내과
Jae Hoon Yang, Joo Young Jung, Chan Soo So, Yu Jin Lim, Seung Yong Han, Sarah Park, Jung Han Kim, Mina Hur, Gyung Kyu Lee, Jung Weon Shim, Young Iee Park
Division of Internal Medicine, Hangang Sacred Heart Hospital, Division of Laboratory Medicine, GangNam Sacred-heart Hospital, Division of Laboratory Medicine, Division of Radiology,Division of Pathology, Hangang Sacred Heart Hospital, Divison of Internal Medicine, National Medical Center, Seoul, Korea
POEMS syndrome is a plasma cell proliferative disorder is characterized by the presence of peripheral neuropathy (P), organomegaly (O), monoclonal gammopathy (M), endocrinopathy or edema (E) and skin change (S). It can be rarely related to multiple myeloma. A 48-year-old man was admitted to our hospital due to paresthesia of both inguinal areas and weakness of both lower extremities. He had a history of Castleman's disease, and showed features of polyneuropathy, multiple osteoblastic lesions, hepatosplenomegaly, pretibial pitting edema, and papilledema. The serum and urine electrophoresis were negative, but urine immunofixagion could detect monoclonal protein. Plasmacytoma was confirmed through the biopsy for the osteoblastic lesions. We present a case of combined POEMS syndrome and multiple myeloma with positive M protein only on immunofixation in order to share our experience with physicians and specialists. (Korean J Hematol 2008;43:253-257.)
Keywords: POEMS syndrome, Multiple myeloma, Osteoblastic lesion
Haerim Chung, Hyunsoo Cho
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