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Primary Hematology PDF

473 Pages·2001·31.63 MB·English
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PRIMARY HEMATOLOGY PRIMARY HEMATOLOGY Edited by AYALEW TEFFERI, MD Consultant, Division o[H ematology and Internal Medicine, Mayo Clinic and Mayo Foundation; Associate Professor o[M edicine, Mayo MedicalSchool; Rochester, Minnesota Springer Science+Business Media, LLC ISBN 978-1-61737-122-6 ISBN 978-1-59259-228-9 (eBook) DOI 10.1007/978-1-59259-228-9 Copyright © 2001 Springer Science+Business Media New York. Originally published by Mayo Foundation for Medical Education and Research in 2001. Softcover reprint ofthe hardcover 1s t edition 2001 For additional copies, pricing for bulk purchases, and/or information about other Humana titles, contact Humana at 999 Riverview Drive, Suite 208, Totowa, NJ 07512 or at any ofthe following numbers: Tel: 973-256-1699; Fax: 973-256-8341; E-mail: [email protected] or visit our website at http://humanapress.com All rights reserved. This book is protected by copyright. No part of it may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, photocopying, recording, or otherwise, without written permission from Mayo Foundation. As new scientific information becomes available through basic and clinical research, recommended treatments and drug therapies undergo changes. The authors and publisher have made all reasonable attempts to make this book accurate, up to date, and in accord with accepted standards at the time of publication. The authors, editor, and publisher are not responsible for errors or omissions or for consequences from application ofthe book, and make no warranty, expressed or implied, in regard to the contents ofthe book. Any practice described in this book should be applied by the reader in consultation with a physician and taking regard ofthe unique circumstances that may apply in each situation. The reader is advised always to check product information (package inserts) for changes and new information regarding dose and contraindications before administering any drug. Caution is especially urged when using new or infrequently ordered drugs. Nothing in this publication implies that Mayo Clinic endorses the products or equipment mentioned in this book. All artic\es, comments, opinions, conclusions, or recommendations are those ofthe author(s) and do not necessarily reflect the views ofthe publisher or of Mayo Clinic. Cover design by Patricia F. Cleary. Cover illustration by Garry Post. This publication is printed on acid-free paper. ® ANSI Z39.48-1984 (American National Standards Institute) Permanence of Paper for Printed Library Materials. Photocopy Authorization PoIicy: Authorization tophotocopy items for internal orpersonal use, orthe internat orpersonal use ofspecific clients, is granted by Humana Press Inc., provided that the base fee of US $10.00 per copy, plus US $00.25 per page, is paid directly to the Copyright Clearance Center at 222 Rosewood Drive, Danvers, MA 01923. For those organizations that have been granted a photocopy Iicense from the CCC, a separate system ofpayment has been arranged and is acceptable to Humana Press Inc. The fee code for users ofthe Transactional Reporting Service is: [0-89603-664-2/01 $10.00 + $00.25]. 10 9 8 7 6 5 4 3 2 I Library of Congress Cataloging-in-Publication Data PREFACE The discipline ofhematology is enriched by tremendous diversity in pathology and its close identification with molecular biology. Routine clinical practice often involves the diagnosis and management of anemia, sickle cell disorders, hypercoagulable states, and monoclonal gamrnopathy ofundetermined significance. Hematologic malignancies, in cluding lymphoma and leukemia, are some ofthe most treatable cancers, and treatment outcome has been improved by the use of hematopoietic stern cell transplantation. He matologists, oncologists, cardiologists, intemists, and family practitioners are all equally interested in the problems ofthrombosis and bleeding. Transfusion medicine, the use of hematopoietic growth factors, and cancer chemotherapy have all become integral com ponents ofhematology practice. A holistic approach to patient care requires so me back ground information on ethics and statistics. This book was written with all of these considerations in mind. I thank the authors ofthe chapters for their diligence in providing fine contributions. I am appreciative of the efforts of the Section of Scientific Publications at Mayo Clinic in the production ofthis book, especially Virginia A. Dunt, Mary L. Schwager, Mary K. Horsman, Roberta J. Schwartz, and LeAnn M. Stee. Ayalew Tefferi, M.D. v To Dr. Rohert L. Phyliky and Dr. H. Clark Hoagland decent human beings, master clinicians, and loyal friends LIST OF COLOR PLATES Color plates appear in an insert foIlowing p. 242. Platel: Chapter 3, Fig. IB. Hemoglobin moleeule. Plate 2: Chapter 3, Fig. lC. Globin genes. Plate 3: Chapter 3, Fig. 2A Peripheral smear-ß-thalassemia minor. Plate 4: Chapter 3, Fig. 2B. Peripheral smear-ß-thalessemia major. Plate 5: Chapter 3, Fig. 2C. Peripheral smear-hemoglobin H disease. Plate 6: Chapter 4, Fig. 2A. Peripheral smear-sickle ceIl disease. Plate 7: Chapter 7, Fig. 1. Ecchymoses and petechiae from severe thrombocy topenia. Plate 8: Chapter 7, Fig. 2. Platelet rosetting in the presence of EDT A. Plate 9: Chapter 10, Fig. 2. Facial plethora in a patient with polycythemia vera. Plate 10: Chapter 10, Fig. 3. Retinal vein distention in a patient with poly cythemia vera, before and after phlebotomy. Plates 11, 12: Chapter 10, Fig. 4A,B. Massive splenomegaly in a patient with myelofibrosis. Plate 13: Chapter 11, Fig. 1. Dimorphie red ceIls. Plate 14: Chapter 11, Fig. 2. Pseudo Pelger-Huet granulocyte. Plate 15: Chapter 11, Fig. 3. Dyserythopoiesis seen in bone marrow aspirate. Plate 16: Chapter 14, Fig. 1. Heterogeneity in the hematopoietic stern ceIl origin of acute myelogenous leukemia (AML). Plate 17: Chapter 15, Fig. 2. Blood and marrow transplantation (BMT) process. Plate 18: Chapter 15, Fig. 4A. The human leukocyte antigen gene system on the short arm of chromosome 6 consists of the class I region of A and B loci as weIl as other loci and the class 11 region of D loci. The class 11 region contains genes of the complement system. Plate 19: Chapter 15, Fig. 6A. Chronic graft-versus-host disease with lichenoid and sclerodermatous changes in the face and scalp with alopecia. Plate 20: Chapter 15, Fig. 6B. Lichenoid hyperpigmentation of the back. Vll CONTENTS Preface ............................................................................................................................ v List of Color Plates ..................................................................................................... vii Contributors ................................................................................................................ xiii I 1 ANEMIA AND OTHER CYTOPENIAS ...................................... A Practical Approach to the Diagnosis of Anemia .......................... 3 Ayalew Tefferi, MD 2 Specific Anemia Syndromes and Their Management.. .................. 21 Ayalew Tefferi, MD 3 The Thalassemia Syndromes and the Hemoglobinopathies .......... 41 Angela Dispenzieri, MD 4 Sickle Cell Disorders ...................................................................... 65 Angela Dispenzieri, MD 5 Practical Aspects in the Diagnosis and Management of Aplastic Anemia ..................................................................... 83 RafaelFonseca, MD 6 Differential Diagnosis ofNeutropenia ........................................... 93 Costas L. Constantinou, MD 7 Causes and Management of Isolated Thrombocytopenia ............ 105 Gerardo Colon-Otero, MD 11 PRIMARY AND SECONDARY MYELOPROLIFERATIVE DISORDERS .... ............ ..................... ............. 117 8 An Approach to the Patient With Erythrocytosis ......................... 119 Aya/ew Tefferi, MD 9 Differential Diagnosis and Management ofThrombocytosis ...... 129 Lawrence A. So/berg, Jr., MD, PhD 10 Chronic Myeloproliferative Diseases: Polycythemia Vera and Agnogenic Myeloid Metaplasia ........ 137 Ayalew Tefferi, MD 11 An Approach to the Patient With Myelodysplasia ....................... 149 Pierre Noel, MD 12 The Eosinophil and Eosinophilia .................................................. 161 Joseph H. Butterfieid, MD ix x Contents III LEUKEMIAS AND HEMATOPOIETIC STEM CELL 173 TRANSPLANTATION .............................. ......... 13 Leukocytosis and the Chronic Leukemias ................................... 175 Ayalew TeJJeri, MD 14 Acute Leukemia ............................................................................ 193 Mark R. Litzow, MD 15 Blood and Marrow Transplantation .............................................. 209 Mark R. Litzow, MD IV 229 LYMPHOID AND PlASMA CELL DISORDERS •••••••••••••••••••• 16 Lymphadenopathy ......................................................................... 231 Thomas M. Habermann, MD 17 Hodgkin' s Disease and N on-Hodgkin' s Lymphoma ................... 241 Thomas M. Habermann, MD 18 An Evaluation of Patients With Monoclonal Gammopathies ...... 255 Robert A. Kyle, MD 19 Multiple Myeloma and Related Disorders ................................... 269 Robert A. Kyle, MD V 289 THROMBOTIC AND BLEEDING DISORDERS •••••••••••••••••••••• 20 An Overview of the Hemostatic System and Interpretation of Common Screening Coagulation Tests ............................... 291 Rajiv K. Pruthi, MD 21 Bleeding Disorders: An Overview and Clinical Practice ........... 303 Rajiv K. Pruthi, MD 22 Thrombogenesis and Thrombotic Disorders ................................ 317 Rajiv K. Pruthi, MD VI 337 MISCELLANEOUS TOPICS IN HEMATOLOGY •••••••••••••••••••• 23 Transfusion Medicine: Practical Issues ....................................... 339 S. Breanndan Moore, MD 24 Hereditary Hemochromatosis: A Disease for All Physicians ..... 351 Virgil F. Fairbanks, MD 25 Hematologic Manifestations of HIV Disease .............................. 365 Zelalem Ternesgen, MD 26 Hematopoietic Growth Factors in Clinical Practice .................... 371 Pierre Noe/, MD 27 A Primer of Chemotherapy ........................................................... 379 Alex A. Adjei, MD, PhD Contents Xl 28 An Approach to Porphyria ............................................................ 407 Lawrence A. So/berg, Jr., MD, PhD 29 Ethical Issues in the Care of Patients With Hematologic Diseases .................................................................................... 415 C. Christopher Hook, M.D. 30 Statistical Methods Frequently Used in Hematology Research .................................................................................... 431 Georgene Schroeder, MS Index ........................................................................................................................... 451

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The discipline of hematology ranges widely from the diagnosis and management of anemia to hematologic malignancies and transfusion medicine, and involves significant ethical issues and problems in statistical interpretation. In Primary Hematology, Ayalew Tefferi, MD, and a team of authoritative prac
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