PathologyAtlas

Waldenström macroglobulinemia

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plasmacytoid lymphocyte

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MYD88 mutation¤ÈWaldenstroem macroglobulinemia

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WM/LPL¤Î¼£ÎÅ up to date

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*1  Waldenström J:Incipient myelomatosis or'essential'¡¡hyperglobulinemia with fibrinogenepenia- a new syndrome? Acta Med Scand 117:216-247, 1944
*2  WHO classification of tumors of haematopoietic and lymphoid tissues 4th Ed, 2008, pp194-195
*3  Owen RG, et al., Clinicopathological definition of Waldenström's macroglobulinemia: consensus panel recommendations from the Second¡¡International Workshop on Waldenström's Macroglobulinemia.Semin Oncol. 2003¡¡Apr;30(2):110-5.
*4  K.Foucar Bone marrow pathology 2nd Ed.ASCP, pp426-429, 2002
*5  Arun Vijay et al., Waldenstöm macroglobulinemia Blood 109:5096-5103,2007
*6  Owen et al., Am J Clin Pathol 116:420-428, 2001
*7  San Miguel JF et al., Semin Oncol 30: 187-195, 2003
*8  Owen RG et al., Semin Oncol 30: 110-115
*9  Treon SP et al., MYD88 L265P somatic mutation in Woldenstrom's macroglobulinemia N Engl J Med 2012; 367: 826-33
*10  Treon SP, et al, MYD88 L265P somatic mutation in Waldenstrom's macroglobulinemia. N Engl J Med. 2012 Aug 30;367(9):826-33.
*11  Hunter ZR, et al, The genomic landscape of Waldenstrom macroglobulinemia is characterized by highly recurring MYD88 and WHIM-like CXCR4 mutations, and small somatic deletions associated with B-cell lymphomagenesis. Blood. 2014 Mar 13;123(11):1637-46.
*12  Treon SP et al., Update on treatment recommendations from the Third International Workshop on Waldenstrom's macroglobulinemia. Blood.¡¡107(9):3442-3446. Epub 2006

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Last-modified: 2020-11-23 (·î) 17:57:45 (64d)