Multiple Myeloma: Diagnosis and Treatment by Robert A. Kyle M.D., S. Vincent Rajkumar M.D. (auth.), Morie

By Robert A. Kyle M.D., S. Vincent Rajkumar M.D. (auth.), Morie A. Gertz, S. Vincent Rajkumar (eds.)

This is a accomplished, cutting-edge consultant to the prognosis, therapy, and biology of a number of myeloma and similar plasma problems. Edited and written by way of a multidisciplinary crew of well-known gurus from the Mayo hospital, it provides transparent directions on analysis and remedy and covers all points of a number of myeloma, from molecular category and prognosis, to probability stratification and remedy. heavily similar plasma telephone issues corresponding to solitary plasmacytoma, Waldenstrom macroglobulinemia, and light-weight chain amyloidosis are mentioned intimately in addition. The e-book addresses usually ignored themes, together with the position of radiation remedy, vertebral augmentation, and supportive care.

Our realizing of this workforce of issues is constructing at an remarkable fee, and Multiple Myeloma meets the necessity between oncologists and hematologists for a transparent, well timed, and authoritative source on their biology, prognosis, and treatment.

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Extra resources for Multiple Myeloma: Diagnosis and Treatment

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There are some clues. It is a histone methyltransferase for H3K36me2, and when over-expressed results in a global increase in H3K36 methylation, and a decrease in H3K27 4 Pathogenesis of Multiple Myeloma methylation, which most likely is the cause of the many changes in gene expression observed in t(4;14) tumors [15, 20–22]. In addition, it recently has been determined that MMSET has a role in DNA repair. Following DNA damage MMSET is phosphorylated on Ser102 by ATM and is recruited to sites of double-strand breaks (DSB) where it results in methylation of H4K20 that is required for recruitment of p53 binding protein (53BP1).

Am J Clin Pathol. 2012;138(4): 609–13. 26. Bradwell AR, Harding SJ, Fourrier NJ, Wallis GLF, Drayson MT, Carr-Smith HD, et al. Assessment of monoclonal gammopathies by nephelometric 25 measurement of individual immunoglobulin kappa/ lambda ratios. Clin Chem. 2009;55(9):1646–55. 27. Donato LJ, Zeldenrust SR, Murray DL, Katzmann JA. A 71-year-old woman with multiple myeloma status after stem cell transplantation. Clin Chem. 2011;57(12):1645–8. 28. Katzmann JA, Snyder MR, Rajkumar SV, Kyle RA, Therneau TM, Benson JT, Dispenzieri A.

Second malignancies after multiple myeloma: from 1960s to 2010s. Blood. 2012;119:2731–7. 4 Pathogenesis of Multiple Myeloma Marta Chesi and P. Leif Bergsagel Introduction Multiple myeloma (MM) is monoclonal tumor of antibody secreting plasma cells (PC) in the bone marrow (BM), that is often diagnosed by the presence of a typical M-spike by serum protein electrophoresis (SPEP), or by free light chains in the urine. Its symptomatic phase is associated with significant end organ damage including lytic bone lesions, anemia, loss of kidney function, immunodeficiency, and amyloid deposits in various tissues [1].

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