Congenital cystic lung disease : comprehensive understanding of its diagnosis and treatment from fetus to childhood / Haruhiko Sago, Hiroomi Okuyama, Yutaka Kanamori, editors.

This book offers readers a comprehensive understanding of congenital cystic lung disease based on a novel classification system recently proposed by leading researchers in the field. Presented in detail here, it includes various aspects, from fetal diagnosis and treatment to postnatal diagnosis and...

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Bibliographic Details
Other Authors: Sago, Haruhiko, Okuyama, Hiroomi, Kanamori, Yutaka
Format: eBook
Language:English
Published: Singapore : Springer, 2020.
Subjects:
Online Access:Click for online access
Table of Contents:
  • Intro
  • Preface
  • Contents
  • 1: Novel Classification of Congenital Cystic Lung Disease
  • 1.1 Introduction
  • 1.2 Novel Classification Based on the Embryology
  • 1.3 Pathology Secondary to Lung Maldevelopment
  • 1.4 Precise Definition of Each Entity of CCLD and Exclusion of the Unfit Lesions
  • 1.5 Future Aspect of the Novel Classification
  • References
  • 2: Epidemiology of Congenital Cystic Lung Disease: From Japan Nationwide Survey
  • 2.1 Perinatal Clinical Features
  • 2.2 Later Onset of Clinical Symptoms in Asymptomatic Neonates
  • 2.3 Surgery, Complications, and Clinical Outcome
  • 2.4 Respiratory Function Measured During Late Postoperative Period
  • 2.5 Lung Lesions and Pathological Diagnosis
  • 2.6 Discussion
  • References
  • 3: Fetal Diagnosis and Therapy for Congenital Cystic Lung Disease
  • 3.1 Introduction
  • 3.2 Prenatal Diagnosis of CLCD
  • 3.2.1 Origin of the Blood Supply
  • 3.2.2 Appearance of the Lung Cyst
  • 3.2.3 Lung Cystic Lesion Size
  • 3.2.4 Presence of Hydrops and Changes in the Appearance
  • 3.3 Fetal Therapy
  • 3.3.1 TAS
  • 3.3.2 Fetal Surgical Resection
  • 3.3.3 Maternal Steroid Therapy
  • 3.3.4 Other Fetal Therapies
  • References
  • 4: Fetal Diagnostic Imaging of Congenital Cystic Lung Disease
  • 4.1 Introduction
  • 4.2 Safety, Magnetic Fields, and Gestational Age in Fetal MRI
  • 4.3 Fetal MR Image Acquisition Technique and Normal Lung Anatomy
  • 4.4 Image Findings
  • 4.4.1 Congenital Pulmonary Airway Malformation (CPAM)
  • 4.5 Bronchopulmonary Sequestration (BPS)
  • 4.6 Bronchial Atresia (BA)
  • 4.7 Congenital Lobar Emphysema (CLE)
  • 4.8 Congenital Bronchogenic Cyst
  • 4.9 Summary
  • References
  • 5: Perinatal Care for Severe Congenital Pulmonary Airway Malformation
  • 5.1 Introduction
  • 5.2 Prenatal Management and Clinical Course
  • 5.2.1 Classification Based on Pathological Findings and Fetal Sonographic Appearance
  • 5.2.2 Evaluation of Cystic Lesion Size Using Fetal Ultrasonography
  • 5.2.3 Treatment of Fetuses with CPAM
  • 5.2.4 Response to Fetal Treatment and Condition Just Before Birth
  • 5.3 Management of Neonates with CPAM at Birth and Infancy
  • 5.3.1 Emergency Surgery Strategy
  • 5.3.2 Points and Pitfalls of Each Department's Role in Emergency Surgery Strategy for Neonates with Severe CPAM
  • 5.3.2.1 Department of Obstetrics for Fetal Medicine
  • 5.3.2.2 Department of Neonatology
  • 5.3.2.3 Department of Anesthesia
  • 5.3.2.4 Department of Surgery
  • 5.4 Management of Patients with CPAM in Infancy and Childhood
  • 5.5 Discussion and Future Perspective
  • References
  • 6: Postnatal Imaging Diagnosis of Congenital Cystic Lung Disease
  • 6.1 Introduction
  • 6.2 Diagnostic Modalities
  • 6.2.1 Chest Radiography
  • 6.2.2 Computed Tomography: CT
  • 6.2.3 Magnetic Resonance Imaging: MRI
  • 6.2.4 Ultrasound: US
  • 6.3 Bronchial Obstruction
  • 6.3.1 Congenital Bronchial Atresia