Specialty Imaging: HRCT of the Lung 2e

  • 저   자 : Santiago Martínez-Jim
  • 역   자 :
  • 출판사 : Elsevier
  • ISBN(13) : 9780323524773
  • 발행일 : 2017  /   2판   /   544 페이지
  • 상품코드 : 25957
  • 적립금: 4,968
276,000248,400

Part of the highly regarded Specialty Imaging series, this fully updated second edition by Drs. Santiago Martínez-
Jiménez, Melissa L. Rosado-de-Christenson, and Brett W. Carter, reflects the many recent changes in HRCT diagnostic
interpretation. An easy-to-read bulleted format and state of the art imaging examples guide you step-by-step through
every aspect of thin-section CT and HRCT in the evaluation of patients with suspected lung disease. This book is an
ideal resource for radiologists who need an easily accessible tool to help them understand the indications, strengths,
and limitations of HRCT in their practice.
Superb illustrations with comprehensive captions display both typical and variant findings on HRCT scans


Introductory sections are specifically designed to lead the general radiologist to differential diagnoses from
specific imaging findings, pathologic patterns, or from the disease/pathology itself


Time-saving bulleted format distills essential information for fast and easy comprehension


Expert Consult™ eBook version included with purchase. This enhanced eBook experience allows you to search all of the
text, figures, videos, and references from the book on a variety of devices.
Updated content includes changes in HRCT interpretation and novel disease processes such as DIPNECH, new
classification of idiopathic interstitial pneumonias, airway-centered interstitial fibrosis, light-chain deposition
disease, and interstitial pneumonia with autoimmune features (IPAF)


Fully revised throughout with new references, images, and histopathologic correlations



목차


SECTION 1: Fundamentals of HRCT

Overview of HRCT

Approach to HRCT Interpretation



Anatomy

Secondary Pulmonary Lobule

Gravitational Changes (Dependent Atelectasis)

Age-Related Changes

Normal Inspiration & Expiration



Terminology and Signs

Micronodules

Acinar Nodules

Tree-in-Bud Opacities

Ground-Glass Attenuation

Crazy-Paving Pattern

Mosaic Attenuation Pattern & Air-Trapping

Head Cheese Sign

Signet Ring Sign

Halo Sign

Reverse Halo Sign

Finger-in-Glove Sign

Honeycombing

Cyst

Flame-Shaped Nodules



Distribution

Peribronchovascular

Centrilobular

Perilymphatic

Random

Peripheral



SECTION 2: Pathological Patterns of Injury

Approach to Pathological Patterns of Injury

Diffuse Alveolar Damage

Diffuse Alveolar Hemorrhage With Capillaritis

Organizing Pneumonia

Pulmonary Fibrosis (Honeycombing)

Constrictive Bronchiolitis (Pathology)

SECTION 3: Large-Airway Disease



Approach to Large-Airway Disease

Bronchiectasis

Allergic Bronchopulmonary Aspergillosis

Williams-Campbell Syndrome

Mounier-Kuhn Syndrome

Bronchocentric Granulomatosis



SECTION 4: Small-Airways Disease

Approach to Small-Airways Disease

Infectious Bronchiolitis

Diffuse Aspiration Bronchiolitis

Respiratory Bronchiolitis

Follicular Bronchiolitis

Hypersensitivity Pneumonitis

Diffuse Panbronchiolitis

Idiopathic Constrictive Bronchiolitis

Swyer-James Syndrome

Bronchiolitis Obliterans Syndrome

DIPNECH



SECTION 5: Infection

Approach to Infection

Bacterial Pneumonia

Parasitic Infection

Viral Pneumonia

Angioinvasive Aspergillosis

PCP Pneumonia

Tuberculosis

Nontuberculous Mycobacterial Infection



SECTION 6: Pneumoconiosis

Approach to Pneumoconiosis

Silicosis & Coal-Worker's Pneumonconiosis

Asbestosis

Beryliosis

Talcosis

Hard-Metal Pneumoconiosis



SECTION 7: Neoplasms

Approach to Neoplasms

Invasive Mucinous Adenocarcinoma (Diffuse)

Lymphangitic Carcinomatosis

Hematogenous Metastases

Endovascuar Metastases and Tumor Emboli

Kaposi Sarcoma

Lymphangioleiomyomatosis

Reactive Lymphoproliferative Disorders

Neoplastic Lymphoproliferative Disorders



SECTION 8: Interstital Pneumonias

Approach to Interstitial Pneumonias

Idiopathic Pulmonary Fibrosis (Idiopathic UIP)

Idiopathic Nonspecific Interstitial Pneumonia

Cryptogenic Organizing Pneumonia

Acute Exacerbation of Interstitial Lung Disease

Acute Interstitial Pneumonia

Idiopathic Lymphoid Interstitial Pneumonia

Idiopathic Pleuroparenchymal Fibroelastosis

Airway-Centered Interstitial Fibrosis

Interstitial Pneumonia With Autoimmune Features (IPAF)

Approach to Smoking-Related Interstitial Lung Diseases

"Respiratory Bronchiolitis, Interstitial Lung Disease"

Desquamative Interstitial Pneumonia

Combined Pulmonary Fibrosis and Emphysema



SECTION 9: Autoimmune Diseases

Approach to Autoimmune Diseases

"Connective Tissue Disease, Interstitial Lung Disease (CTD-ILD)"

Rheumatoid Arthritis

Progressive Systemic Sclerosis

Dermatomyositis/Polymyositis

Sjögren Syndrome

Mixed Connective Tissue Disease

Systemic Lupus Erythematosus

Granulomatosis With Polyangiitis (GPA)

Eosinophilic Granulomatosis With Polyangiitis (E-GPA)

Microscopic Polyangiitis

Ankylosing Spondylitis

Inflammatory Bowel Disease



SECTION 10: Vascular Disease

Approach to Vascular Disease

Cardiogenic Pulmonary Edema

Hepatopulmonary Syndrome

Pulmonary Hypertension

Pulmonary Venoocclusive Disease

Pulmonary Capillary Hemangiomatosis

Talc & Cellulose Granulomatosis



SECTION 11: Inhalational, Inflammatory, Metabolic, & Post Treatment

Approach to Inhalational, Inflammatory, Metabolic, & Post Treatment



Aspiration/Inhalation

Spectrum of Aspiration-Related Disorders

Lipoid Pneumonia

Inhalational Injury



Inflammatory

Sarcoidosis

Histiocytic Disorders

Eosinophilic Disorders



Metabolic or Degenerative

Amyloidosis

Light-Chain Deposition Disease

Pulmonary Alveolar Proteinosis

Metastatic Pulmonary Calcification

Diffuse Pulmonary Ossification (Dendriform & Nodular)

Emphysema

Hemosiderosis



Post Treatment

Radiation-Induced Lung Disease

Drug-Induced Lung Disease



SECTION 12: Congenital

Approach to Congenital

Familial Idiopathic Pulmonary Fibrosis

Birt-Hogg-Dubé Syndrome

Hermansky-Pudlak Syndrome

Tuberous Sclerosis

Neurofibromatosis

Alveolar Microlithiasis

Alpha-1 Antitrypsin Deficiency

Primary Ciliary Dyskinesia

Primary Immunodeficiencies

Chronic Granulomatous Disease

Cystic Fibrosis

Children's Interstitial Lung Disease (chILD)

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