Download Amyloid and Related Disorders: Surgical Pathology and by Per Westermark M.D., Ph.D. (auth.), Maria M. Picken MD, PhD, PDF

By Per Westermark M.D., Ph.D. (auth.), Maria M. Picken MD, PhD, FASN, Ahmet Dogan, M.D., Ph.D., Guillermo A. Herrera, M.D. (eds.)

ISBN-10: 1607613883

ISBN-13: 9781607613886

Abnormal proteins are identified to be linked to a variety of pathologies. such a lot particularly, those contain amyloidoses, monoclonal protein deposits linked to plasma mobilephone dyscrasia/multiple myeloma, cryoglobulins and numerous comparable geared up and non-organized deposits.

Amyloid and comparable Disorders provides an outline of the main

recent advancements during this region together with scientific presentation, etiology, pathogenesis, and differential prognosis. the reason for varied cures, together with transplantation, is mentioned and tissue prognosis (its pitfalls and techniques for heading off them) and laboratory aid are incorporated. The involvement of all significant organ structures together with renal/genitourinary, cardiac, gastrointestinal, pulmonary, peripheral nerve/central worried approach, smooth tissue and bone marrow pathology is roofed. This process presents a unifying idea of those pathologic procedures, that have systemic involvement, and that have, hitherto, no longer been universally preferred. knowledge of those ailments between a much broader viewers of pathologists may well bring up the speed in their analysis in addition to that of prior prognosis. This quantity should be priceless to really expert and normal pathologists in addition to cytopathologists; different doctors can also reap the benefits of this concise replace at the systemic amyloidoses.

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Additional info for Amyloid and Related Disorders: Surgical Pathology and Clinical Correlations

Sample text

Palladini G, Lavatelli F, Russo P, et al. Circulating amyloidogenic free light chains and serum N-terminal natriuretic peptide type B decrease simultaneously 142. 143. 144. 145. 146. 147. 148. 149. 150. 151. 152. 153. 154. 155. 156. 157. 27 in association with improvement of survival in AL. Blood. 2006;107:3854–8. Trinkaus-Randall V, Walsh MT, Steeves S, et al. Cellular response of cardiac fibroblasts to amyloidogenic light chains. Am J Pathol. 2005;166:197–208. Monis GF, Schultz C, Ren R, et al.

2001;410: 165–6. 5. Chiti F, Dobson CM. Amyloid formation by globular proteins under native conditions. Nat Chem Biol. 2009;5:15–22. 6. Powers ET, Morimoto RI, Dillin A, et al. Biological and chemical approaches to diseases of proteostasis deficiency. Annu Rev Biochem. 2009;78:959–91. 7. Westermark GT, Westermark P. Serum amyloid A and protein AA: molecular mechanisms of a transmissible amyloidosis. FEBS Lett. 2009;583:2685–90. 8. Heegaard NH. Beta(2)-microglobulin: from physiology to amyloidosis.

179. Gertz MA, Merlini G. Definition of organ involvement and tratment response in immunoglobulin light chain amyloidosis (AL): a consensus opinion. Amyloid. 2010;17:48–9. 180. Merlini G, Marciano S, Gasparro C, et al. The Pavia approach to clinical protein analysis. Clin Chem Lab Med. 2001;39:1025–8. 181. Palladini G, Russo P, Bosoni T, et al. Identification of amyloidogenic light chains requires the combination of serum-free light chain assay with immunofixation of serum and urine. Clin Chem.

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