Clinical Atlas of Interstitial Lung Disease - Tatjana Peros-Golubicic, medicalheaven radiology

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Clinical Atlas of Interstitial Lung Disease
Tatjana Pero
ˇ
-Golubiˇic´, MD, PhD, and
Om P. Sharma, MD, FRCP
Clinical Atlas of
Interstitial
Lung Disease
Foreword by Talmadge E. King, Jr., MD
Tatjana Peroˇ-Golubiˇi ´, MD, PhD
University of Zagreb
Medical School
University Hospital for Lung Diseases “Jordanovac”
Zagreb
Croatia
Om P. Sharma, MD, FRCP
Keck School of Medicine at University of Southern California
Los Angeles, California
USA
British Library Cataloguing in Publication Data
Peroˇ-Golubiˇi ´, Tatjana
Clinical atlas of interstitial lung disease
1. Interstitial lung diseases—Atlases
I. Title II. Sharma, Om P.
616.2′4
ISBN-13: 9781846283208
ISBN-10: 1846283205
Library of Congress Control Number: 2005938495
ISBN-10: 1-84628-320-5 e-ISBN-10: 1-84628-326-4
ISBN-13: 978-1-84628-320-8 e-ISBN-13: 978-1-84628-326-0
Printed on acid-free paper
© Springer-Verlag London Limited 2006
Apart from any fair dealing for the purposes of research or private study, or criticism or review, as permitted
under the Copyright, Designs and Patents Act 1988, this publication may only be reproduced, stored or trans-
mitted, in any form or by any means, with the prior permission in writing of the publishers, or in the case of
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987654321
Springer Science+Business Media, LLC
Foreword
The interstitial lung diseases, also called diffuse parenchymal lung diseases, are a diverse
group of pulmonary disorders classified together because of similar clinical, roentgeno-
graphic, physiologic, or pathologic features. During the past 50 years, we have experi-
enced remarkable advances in the classification, diagnosis, and management of these
diseases. Technological advances, particularly high-resolution computed tomography,
bronchoalveolar lavage, and video-assisted thoracic surgery, have provided access to
information that has vastly improved our understanding of these entities. In addition,
genetic medicine, the use of new technologies (e.g., microarrays, mass spectroscopic
analysis of proteins, and laser capture microdissection) and the development of animal
models have led to better understanding of the pathogenesis of these disorders.
Unfortunately, patients with diffuse parenchymal lung disease continue to present a
difficult diagnostic and management challenge to clinicians. A major reason is that the
topic of “interstitial lung disease” is vast and difficult to grasp. Some 25 years ago when
I first became interested in interstitial lung diseases, there was no ready source of infor-
mation relating specifically to these processes. Even today, there is a need for a compre-
hensive, yet easy to read, manual of the key information about the important interstitial
lung diseases.
The purpose of this atlas is to provide the clinician, from medical student to lung spe-
cialist, with a ready reference helpful in their attempts to master this topic and to provide
guidance in their daily practice. The subject of interstitial lung disease is inherently mul-
tidisciplinary; consequently, the authors have provided a consistent approach to each
entity that includes the key clinical, physiologic, radiologic, and pathologic features.
The
Clinical Atlas of Interstitial Lung Disease
is composed of 37 chapters loosely
divided into six sections. The first section provides a historical background to the inter-
stitial lung diseases and an overview of the basis for recognizing the key features that
allow a specific diagnosis to be achieved. The second section is dedicated to the inter-
stitial lung diseases of unknown etiology, including sarcoidosis, the idiopathic intersti-
tial pneumonias, and eosinophilic pneumonias. The third section describes interstitial
lung diseases of known etiology (e.g., drug-induced, radiation, hypersensitivity pneu-
monitis, and pneumoconioses). The fourth section addresses interstitial lung diseases
associated with the connective tissue diseases and pulmonary vasculitidies. The fifth
section deals with a number of specific entities (e.g., alveolar proteinosis, lymphangi-
oleiomyomatosis, and Langerhans cell histiocytosis). The final section devotes several
chapters to the pulmonary manifestations of systemic diseases, such as paraproteine-
mias, liver and gastrointestinal disease, and malignancy.
We owe a debt of gratitude to all those who were involved in producing this
Clinical
Atlas of Interstitial Lung Disease
. The authors have succeeded in creating a readable,
concise atlas that is up to date and user friendly.
Talmadge E. King, Jr., M.D.
Department of Medicine
University of California San Francisco; and
San Francisco General Hospital
San Francisco, California
v
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