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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5795_Библиотеки_им_академика_М_И_Перельмана.pdf
X
- •Preface for the Second Edition
- •Acknowledgements
- •Contents
- •1: US Physics
- •1.1 US Waves
- •1.2.5 Deflection
- •1.2.6 Focus
- •1.2.7 Resolution
- •1.3.1 Emission
- •1.3.2 Transmission
- •1.3.3 Reception
- •1.3.4 Amplification
- •1.4 Signal Processing
- •1.4.1 Preprocessing
- •1.4.2 Post-Processing
- •1.4.3 Time Gain Compensation (TGC)
- •1.4.5 Gain
- •1.4.6 Frame Rate/Persistence
- •1.5.1 Transducers
- •1.6 Modern US Techniques
- •1.6.1 High-Resolution US (HR-US)
- •1.6.2 Image Compounding
- •1.2.1 Acoustic Impedance
- •1.2.2 Impedance Change
- •1.2.3 Reflection
- •1.2.4 Absorption
- •1.6.3 Harmonic Imaging (HI)
- •1.6.5 US Texture Analysis
- •2: US Methods, Artefacts, Biologic Effects, Practice
- •2.1 A (Amplitude)-Mode
- •2.2 (T)M-Mode (Time-Motion-Mode)
- •2.3 B (Brightness)-Mode
- •2.4 Doppler Sonography
- •2.5 Artefacts
- •2.5.1 General Remarks
- •2.5.2 Common Artefacts
- •2.5.2.1 Side Loop Artefact
- •2.5.2.2 Bowing Artefact
- •2.5.2.3 Noise
- •2.5.2.4 Marginal Shadowing
- •2.5.2.5 Posterior Enhancement—Increased through Transmission
- •2.5.2.6 Reverberation Artefact
- •2.5.2.7 Increment or Slice Thickness/Beam Width Artefact
- •2.5.2.8 Mirror Image Artefact
- •2.5.2.9 Shadowing
- •2.5.2.10 Refraction Artefact
- •2.5.2.11 Anisotropy
- •2.6 Biologic Effects
- •2.6.1 General Remarks
- •2.6.2 Thermal Effects
- •2.6.2.1 Tissue Heating
- •2.6.2.2 Biological Effects, Tissue Heating
- •2.6.3.1 Cavitation
- •2.6.4.1 Specific Risks
- •2.6.5.1 Mechanical Index (MI)
- •2.6.5.2 Thermal Index (TI)
- •2.7.1 Requisites
- •2.7.1.1 Indications
- •2.7.1.2 Environmental Requisites
- •2.7.2 Positioning
- •2.7.3 Device Handling
- •2.7.3.1 General Remarks
- •2.7.4 Transducer Selection
- •2.7.4.1 General Remarks
- •2.7.4.2 Neurosonography (See Chap. 8)
- •2.7.4.4 Chest US (See Chap. 12)
- •2.7.4.5 Abdominal US (See Respective Chapters)
- •2.7.5.1 General Remarks
- •2.7.5.2 Transducer Handling
- •2.7.5.3 Measurements
- •2.8.1 Image Documentation
- •2.8.2 Report
- •2.8.2.2 Diagnosis
- •2.8.2.3 Predefined Reports
- •2.8.2.4 Nomenclature
- •3.1 Doppler Sonography
- •3.1.1 The Doppler Phenomenon
- •3.1.2.1 Continuous Wave Doppler (CW)
- •3.1.2.2 Pulsed Wave Doppler (PW)
- •3.1.2.3 Duplex-Doppler Sonography/Spectral Flow Analysis
- •3.1.2.5 Amplitude-Coded Colour Doppler Sonography (aCDS)
- •3.1.2.6 Other Flow-Sensitive US Techniques
- •3.2.1 Aliasing
- •3.2.2 Spectral Broadening
- •3.2.3 Sample Volume Artefact
- •3.2.4 Filtering Artefacts
- •3.2.5 Scaling Problems
- •3.2.6 Gain-Induced Errors
- •3.2.7 Angle Correction
- •3.2.8 Motion Artefact
- •3.2.9 Twinkling Artefact
- •3.2.10 Others
- •3.3.1 Limitations
- •3.3.2 Interpretation
- •3.4.2 Typical Paediatric 3DUS Applications
- •3.4.2.1 Neonatal Neurosonography
- •3.4.2.7 Other Potential 3D-/4DUS Applications
- •3.4.5 Potential Future Paediatric 3DUS Applications
- •4.1 Contrast-Enhanced Ultrasound (ce-US)
- •4.1.1 Basics
- •4.1.2 ce-US Applications-General Remarks
- •4.1.3 Contrast-Enhanced Voiding Urosonography (ce-VUS)
- •3.4.2.3 Urinary Bladder 3DUS
- •3.4.2.5 Musculoskeletal 3DUS Applications
- •3.4.2.6 Small Part 3DUS Applications
- •4.1.5 Intravenous ce-US (CEUS)
- •4.1.5.2 Dose Recommendations
- •4.1.6 Future ce-US Potential
- •4.2 Ultrasound-/Sonoelastography
- •4.2.1 Methods
- •4.2.1.1 Strain Elastography
- •4.2.1.2 Transient Elastography (TE)
- •4.2.1.3 Shear Wave Elastography (SWE)
- •4.2.2 Applications
- •4.2.2.1 Focal Lesions
- •4.2.2.2 Diffuse Changes
- •4.2.2.3 Possible Indications—Summary
- •5.1 Requirements
- •5.2 Typical Applications
- •6.1 Introduction
- •6.2.1 Urinary Tract Infection (UTI)
- •6.2.3.1 Pelvi-Ureteric Junction Obstruction (PUJO)
- •6.2.3.3 Gross Vesico-Ureteric Reflux (VUR)
- •6.2.4 Urolithiasis (and Nephrocalcinosis)
- •6.2.5 Cystic Kidney Disease (CKD)
- •6.2.6 Torsion (Ovary, Testis)
- •6.2.7 Genital Malformations
- •6.2.8 Renal Hypertension
- •6.3.1 Necrotizing Enterocolitis (NEC)
- •6.3.3 Acute Abdomen
- •6.3.4 Acute Appendicitis
- •6.3.5 Splenomegaly
- •6.3.6 Cholestasis
- •6.3.7 Pancreatitis
- •6.3.8 Biliary Atresia
- •6.3.9 Abdominal Trauma
- •6.3.10 Abdominal Tumours
- •6.4.1 Pneumonia, Pleural Effusion
- •6.4.2 Enlarged Mediastinum
- •6.4.3 Painful Hip/Limping Child: Osteomyelitis
- •7.1 General Considerations
- •7.3.1 Miscellaneous Other Considerations
- •8.1 Requisites
- •8.2 Normal Findings
- •8.2.1 Transfontanellar Access
- •8.2.2 Alternate Access Findings
- •8.2.3 Colour Doppler Sonography (CDS)
- •8.2.4.1 Periventricular Echogenicities
- •8.2.4.2 Ventricular Asymmetry
- •8.2.4.3 Ventriculomegaly
- •8.2.4.4 Cisterna Magna
- •8.2.4.5 Vascular Variations
- •8.3 Pathologic Findings
- •8.3.1 Neural Tube Defects
- •8.3.1.1 Anencephaly
- •8.3.1.3 Arnold Chiari Malformation
- •8.3.1.4 Dandy–Walker Malformations/Spectrum
- •8.3.1.5 Corpus Callosum Malformations
- •8.3.1.6 Lipoma
- •8.3.2.2 Megalencephaly
- •8.3.2.3 Schizencephaly
- •8.3.2.4 Holoprosencephaly
- •Alobar Holoprosencephaly
- •Semilobar Holoprosencephaly
- •Lobar Holoprosencephaly
- •De Morsier Syndrome: Septo-Optic Dysplasia
- •8.3.2.5 Hydranencephaly
- •8.3.3 Phakomatoses
- •8.3.4 Cerebral Cysts
- •8.3.5 Ischemic Encephalopathy
- •8.3.5.1 Preterm Infant
- •8.3.5.2 Global or Diffuse Brain Oedema
- •8.3.6 Other applications of (C)DS:
- •8.3.7 Inflammation
- •8.3.7.2 Postnatal Inflammation
- •8.3.9 Cerebral Haemorrhage
- •8.3.10.1 Vascular Malformations
- •8.3.11 Cerebral Calcifications
- •8.4.1 Introduction
- •8.4.2 Haematoma
- •8.4.4 Skull Fracture
- •8.5 Additional Imaging
- •8.5.1 Plain Film
- •8.5.2 CT
- •8.5.3 MRI
- •8.5.4 Catheter Angiography
- •8.5.5 Additional Supporting Procedures
- •8.6.1 Introduction
- •8.6.2 Normal Findings
- •8.6.3 Sonographically Depictable Pathology
- •9.1 Introduction
- •9.2 Requisites
- •9.4 Indications
- •9.5 Normal Findings
- •9.6.1 Dysraphism
- •9.6.2 Other Associated Pathology
- •9.6.3 Other “Occult” Dysraphisms
- •9.7 Trauma
- •9.8 Tumours and Miscellaneous Others
- •9.10 Additional Imaging
- •10.1.1 Transducers
- •10.1.3 Typical Examinations
- •10.1.3.1 Cervical Lymph Nodes
- •10.1.3.2 Glands
- •10.1.3.3 Cervical Arteries
- •10.1.3.4 Cervical Veins
- •10.1.3.5 Intervention
- •10.2 Normal Findings
- •10.2.1 Lymph Nodes
- •10.2.2 Cervical Glands
- •10.2.2.1 Thyroid Gland
- •10.2.3 Other Cervical Soft Tissues
- •10.2.3.1 Muscles
- •10.2.3.2 Tonsils
- •10.2.3.3 Tongue
- •10.2.3.5 Larynx
- •10.2.4 Cervical Vessels
- •10.3 Pathologic Findings
- •10.3.1 Lymph Nodes
- •10.3.2.1 Malformations
- •Cervical Cyst
- •Dermoid Cyst
- •Duplication Cysts
- •Thymic Cyst
- •Cervical Ectopic Thymus
- •10.3.2.2 Tumours
- •Haemangioma
- •Lymphatic Malformation
- •Other Mesenchymal Tumours
- •Teratoma
- •Other Malignant Tumours
- •10.3.2.3 Abscess Formations
- •10.3.2.4 Traumatic Changes
- •Haematoma (Including Sternocleidomastoid Muscle “Haematoma”)
- •10.3.3 Thyroid Gland
- •10.3.3.1 Cystic Changes
- •10.3.3.2 Malformations
- •10.3.3.3 Inflammation
- •10.3.3.4 Other Conditions
- •Nodular Goitre
- •Amyloid Goitre
- •Adenoma/Carcinoma
- •10.3.4 Salivary Glands (Parotid, Sublingual, Submandibular Gland)
- •10.3.4.1 Inflammation
- •10.3.4.2 Cysts
- •10.3.4.3 Calcifications/Sialolithiasis
- •10.3.4.4 Tumours
- •10.3.5 Cervical Vessels
- •10.3.5.1 Arteriosclerosis
- •10.3.5.2 Dissection
- •10.3.5.3 Stenosis
- •10.3.5.4 Other Vascular Anomalies
- •11.1 Introduction
- •11.2.1 Transducers
- •11.2.2 Standard US Techniques
- •11.2.3 Patient Position
- •11.2.4 Sedation
- •11.4 Normal 2D Echocardiogram Findings
- •11.4.1 Parasternal Views
- •11.4.1.3 Apical Views
- •11.4.2 Subcostal Views
- •11.4.2.1 Sagittal Subcostal View
- •11.5 Other Techniques
- •11.5.1 M (Motion)-Mode Echocardiography
- •11.6 Special Echocardiographic Techniques
- •11.6.1 Transoesophageal Echocardiography (TEE)
- •11.6.2 Three-/Four-Dimensional (3D/4D) Echocardiography
- •11.6.3 Tissue Doppler Imaging (TDI)
- •11.6.4 Contrast-Enhanced US (ce-US/CEUS)
- •11.7 Normal Values
- •11.8 Pathologic Findings
- •11.8.1.1 Atrial Septal Defect (ASD)
- •11.8.1.2 Atrioventricular Septal Defects (AVSD)
- •11.8.1.3 Ventricular Septal Defects (VSD)
- •11.8.2.1 Aortic Valve Stenosis (AS)
- •11.8.2.2 Subaortic Stenosis (Sub-AS)
- •11.8.2.3 Supravalvular Aortic Stenosis
- •11.8.2.4 Aortic Coarctation (CoA)
- •11.8.2.5 Interrupted Aortic Arch
- •11.8.3.1 Isolated Pulmonary Valve Stenosis (PS)
- •11.8.3.2 Subvalvular Pulmonary Stenosis
- •11.8.3.3 Supravalvular Pulmonary Stenosis
- •11.8.4 Miscellaneous Congenital Heart Defects
- •11.8.4.2 Total Anomalous Pulmonary Venous Return (TAPVR)
- •11.8.4.3 Univentricular Heart (UVH)
- •11.8.4.4 Double Outlet Right Ventricle (DORV)
- •11.8.4.5 Ebstein Anomaly
- •11.8.4.6 Cor Triatriatum
- •11.9 Acquired Paediatric Heart Diseases
- •11.9.1 Cardiomyopathies (CMP)
- •11.9.1.1 Hypertrophic CMP
- •11.9.1.2 Hypertrophic Obstructive CMP (HOCMP)
- •11.9.1.3 Dilated (Congestive) CMP
- •11.9.1.4 Restrictive CMP
- •11.9.2 Acute Myocarditis
- •11.9.3 Acute (Infective) Endocarditis
- •11.9.4 Pericarditis/Pericardial Effusion
- •11.9.5 Kawasaki Disease
- •11.9.6 Intracardiac Thrombi
- •11.9.7 Cardiac Tumours
- •11.11 Complementing Investigations
- •11.12.1.1 Typical Orientating Examination
- •11.12.1.2 Typical Clinical Queries
- •12.1 Requisites
- •12.1.1 Transducers
- •12.1.2 Positioning
- •12.1.3 Indications
- •12.2 Normal Findings
- •12.2.1 Chest Wall
- •12.2.2 Breast
- •12.2.3 Pleural Space
- •12.2.4 Diaphragm
- •12.2.5 Lung
- •12.2.6 Mediastinum
- •12.2.6.1 Anterior Mediastinum/Thymus
- •12.2.6.2 Middle Mediastinum
- •12.2.6.3 Posterior Mediastinum
- •12.2.7 (Colour) Doppler Sonography
- •12.2.8 Contrast Enhanced US (ce-US)
- •12.3.2 Congenital Malformations
- •12.3.3 Traumatic Changes
- •12.3.4 Chest Wall Tumours
- •12.3.4.1 Lymphangioma (Venolymphatic Vascular Malformation)
- •12.3.4.2 Lipoma
- •12.3.4.3 Fibroma/Neurofibroma
- •12.3.4.4 Other Tumours
- •12.3.5 Breast
- •12.3.6 Miscellaneous Other Applications
- •12.4.1 Pneumothorax
- •12.4.2 Pleural Effusion
- •12.4.2.1 Empyema
- •12.4.3 Other Pleural Pathology
- •12.5.1 Diaphragmatic Hernia
- •12.5.2 Diaphragmatic Motion Disturbance
- •12.6 Lung Pathology
- •12.6.1 Pneumonia
- •12.6.2 Lung Abscess
- •12.6.3 Atelectasis
- •12.6.5 Sequestration
- •12.6.6 Congenital Cystic Adenomatoid Malformation (CCAM)
- •12.6.7 Cysts
- •12.6.8 Infarction
- •12.8 Additional Imaging
- •13.1 Introduction
- •13.2.1 Preparation
- •13.2.2 Positioning
- •13.2.3 Transducers
- •13.3 Liver
- •13.3.2 Standard Planes
- •13.3.3 Normal Findings
- •13.3.3.1 Structure
- •13.3.3.2 Ligaments
- •13.3.3.3 Hepatic Veins (HV)
- •13.3.3.4 Portal Vein (PV)
- •13.3.3.5 Hepatic Artery (HA)
- •13.3.3.6 Gall Bladder
- •13.3.3.7 Common Bile Duct
- •13.3.3.8 Intrahepatic Bile Ducts
- •13.3.3.9 Doppler Findings
- •Situs Inversus (Abdominalis)
- •Butterfly or Midline Liver
- •13.3.4.2 Inflammatory Conditions
- •Hepatitis
- •Liver Abscess
- •Granulomatous Disease
- •13.3.4.3 Other Parenchymal Liver Disease
- •Fatty Liver/Steatosis
- •Liver Congestion
- •Liver Fibrosis
- •Cirrhotic Liver
- •Portal Hypertension
- •Vascular Malformations
- •Hepatic Vein Thrombosis/Occlusion/Stenosis
- •Portosystemic Shunts
- •13.3.4.5 Liver Trauma
- •Liver Haematoma
- •Contusion
- •Laceration
- •Haemobilia
- •Associated Diaphragmatic Injury
- •Liver Infarction
- •Additional Imaging
- •13.3.4.6 Space-Occupying Liver Lesions
- •Simple Cysts
- •Complicated Cysts
- •Liver Calcifications
- •Intrahepatic Gas
- •Haemangioma
- •Mesenchymal Hamartoma
- •Focal Nodular Hyperplasia (FNH)
- •Hepatic Adenoma
- •Fatty Tumours
- •Hepatoblastoma
- •Hepatocellular Carcinoma
- •Hepatic Sarcomas
- •Metastasis
- •Proliferative Disorders
- •Additional Imaging
- •13.4.1 General Findings
- •13.4.2.1 Intrahepatic Gall Bladder
- •13.4.2.3 Choledochal Cyst
- •13.4.3 Biliary Tract Diseases
- •13.4.3.1 Aerobilia
- •13.4.3.2 Cholestatic Changes/Inspissated Bile/Gallstone
- •13.4.3.3 Sclerosing Cholangitis
- •13.4.3.5 Tumour-like Conditions
- •Polyps
- •Tumours
- •13.4.3.7 Additional Imaging
- •13.5.1 Pretransplant US
- •13.5.1.1 Recipient Evaluation
- •13.5.2 Intraoperative US
- •13.5.3 Postoperative Assessment
- •13.5.4 Typical Complications
- •13.6 Spleen
- •13.6.1 Requisites
- •13.6.2 Positioning
- •13.6.3 Indications
- •13.6.5 Normal Anatomy
- •13.6.6 Normal Variants
- •13.6.6.1 Splenunculus (Accessory Spleen)
- •13.6.7 Malformations
- •13.6.7.1 Asplenia
- •13.6.7.2 Polysplenia Syndrome
- •13.6.7.3 Wandering Spleen
- •13.6.8 Splenomegaly
- •13.6.9 Trauma
- •13.6.10 Splenic Infarction
- •13.6.11.1 Cysts
- •13.7 Pancreas
- •13.7.1 Requisites
- •13.7.2 Indication
- •13.7.4 Normal Findings
- •13.7.5.1 Annular Pancreas
- •13.7.5.2 Pancreas Divisum
- •13.7.6 Inflammation: Pancreatitis
- •13.7.6.1 Oedematous or Reactive Pancreatitis
- •13.7.6.2 Haemorrhagic or Necrotising Pancreatitis
- •13.7.6.3 Chronic Pancreatitis
- •13.7.7 Trauma
- •13.7.8 Space-Occupying Lesions
- •13.7.8.1 Cysts/Pseudocysts
- •13.7.8.2 Tumours
- •13.7.10 Additional Imaging
- •13.8.1 Abdominal Vessels
- •13.8.1.1 Positioning
- •13.8.1.2 Transducers
- •13.8.1.4 US Findings
- •13.8.2 Vascular Pathology
- •13.8.2.1 Thrombosis/Occlusion
- •13.8.2.2 Pelvic Congestion Syndrome
- •13.8.2.3 Mid-Aortic Syndrome
- •13.8.2.4 Retroaortic Left Renal Vein: Nutcracker Syndrome
- •13.8.2.9 Complementing Imaging
- •13.8.3 Retroperitoneal Soft Tissues
- •13.8.3.1 Lymph Nodes
- •13.8.3.2 Retroperitoneal Tumours
- •13.8.3.3 Abdominal Wall
- •14.1 Stomach
- •14.1.1 Requisites
- •14.1.2.1 Access
- •14.1.3 Normal Findings
- •14.1.4 Normal Variants
- •14.1.5 Malformations
- •14.1.5.1 Microgastria
- •14.1.5.2 Pyloric Atresia
- •14.1.5.3 Congenital Hiatal Hernia
- •14.1.6 Pathologic Findings
- •14.1.6.1 Gastro-Oesophageal Reflux (GOER)
- •14.1.6.2 Hypertrophic Pyloric Stenosis (HPSt)
- •14.1.6.3 Other Stomach Conditions
- •14.2 Bowel
- •14.2.3 Normal US Findings
- •14.2.4 Pathology
- •14.2.4.1 Congenital Anomalies
- •14.2.5 Acquired Obstructive Pathology
- •14.2.5.1 Meconium Ileus
- •14.2.5.2 Midgut Volvulus
- •14.2.5.3 Sigma Volvulus
- •14.2.5.4 Hernia
- •14.2.5.5 Intussusception
- •14.2.6 Inflammatory Conditions
- •14.2.6.1 Necrotising Enterocolitis (NEC)
- •14.2.6.2 Gastroenteritis
- •14.2.6.3 Henoch–Schönlein Purpura
- •14.2.6.4 Appendicitis
- •14.2.6.5 Crohn’s Disease
- •14.2.6.6 Colitis
- •14.2.6.7 Other Inflammatory Bowel Conditions
- •14.2.6.8 Bowel Trauma
- •14.2.7 Mesentery
- •14.2.7.1 Mesenteric (Peritoneal) Masses
- •14.2.7.2 Abscesses
- •14.2.7.3 Twisted Appendices Epiploica
- •14.2.8 Mesenteric Lymph Nodes
- •14.2.9 Free Intraperitoneal Air
- •14.2.10 Free Intraperitoneal Fluid: Ascites
- •14.2.11 Mesenteric Vessels
- •15.1 Requisites
- •15.1.1 Indications
- •15.1.2 Preparation
- •15.1.3 Transducers
- •15.1.4 Positioning
- •15.1.5.1 Diuretic US
- •15.1.6 Contrast-Enhanced Voiding Urosonography (ce-VUS)
- •15.2 Normal Findings
- •15.2.1 Bladder
- •15.2.2 Kidney
- •15.2.2.1 Normal Variants
- •Duplex Kidney
- •Ectopic Kidneys
- •Renal Agenesis
- •15.3.1 Congenital Conditions
- •15.3.1.1 Dysplasia/Hypoplasia
- •15.3.1.2 Cystic Renal Disease
- •Inherited/Congenital Cystic Disease
- •Acquired Cystic Kidney Disease
- •Urinary Tract Dilatation (UTD) or Pelvicalyceal Dilatation/Distention (PCD)
- •Pelvi-ureteric Junction Obstruction (PUJO)
- •Uretero-Vesical Junction Obstruction (UVJO)/Obstructive Megaureter (POM/MU)
- •Posterior Urethral Valve (PUV)
- •Vesico-Ureteric Reflux (VUR)
- •Secondary Obstruction
- •15.3.2 Inflammatory Renal Parenchymal Conditions
- •15.3.2.1 Pyelitis
- •15.3.2.2 Acute Pyelonephritis (aPN)/Interstitial Nephritis
- •15.3.2.4 Scarring
- •15.3.2.5 Tuberculosis
- •15.3.2.6 Xanthogranulomatous Pyelonephritis
- •15.3.2.7 Glomerulonephritis/Nephrotic Syndrome
- •15.3.3 Vascular Conditions
- •15.3.3.1 Renal Artery Stenosis
- •15.3.3.2 Arteriovenous Fistula (AVF)
- •15.3.3.3 Infarction
- •15.3.3.4 Renal Vein Thrombosis
- •15.3.4 Nephrocalcinosis
- •15.3.5 Urolithiasis
- •15.3.6 Other Important Renal Parenchymal Disease
- •15.3.6.1 Haemolytic Uremic Syndrome (HUS)
- •15.3.6.2 Glomerulonephritis/Nephrotic Syndrome
- •15.3.6.3 Scars, Cirrhotic Kidney
- •15.3.7 Renal Failure (RF)
- •15.3.8 Renal/Urinary Tract Trauma
- •15.3.9 Renal Tumours
- •15.3.9.1 Benign Tumours
- •15.3.9.2 Pre- or Semi-Malignant Tumours
- •15.3.9.3 Malignant Tumours
- •15.4.1 Renal Biopsy
- •15.4.2 Drainage/Nephrostomy
- •15.4.3 Postoperative Imaging
- •15.4.3.1 After VUR Treatment
- •Cystoscopic Treatment
- •Antireflux Surgery
- •15.4.3.2 Findings after Pyeloplasty
- •15.4.3.3 After Various Interventions
- •15.5 Renal Transplant
- •15.5.2 Pathologic US Findings
- •15.6.1 General Remarks
- •15.6.2 Typical Normal US Finding
- •15.6.3 Pathologic Findings
- •15.6.3.1 Adrenal Gland Haemorrhage
- •15.6.3.2 Inflammatory Condition
- •15.6.3.3 Tumours
- •Adrenal Cysts
- •Adrenal Adenoma
- •Neuroblastoma
- •Ganglioneuroma
- •Phaeochromocytoma
- •Adrenal Carcinoma
- •15.7.1 Requisites
- •15.7.2 Pathologic Findings
- •15.7.2.1 Atypical Shape (Neurogenic Bladder, “Valve Bladder”)
- •15.7.2.2 Polyps
- •15.7.2.3 Bladder Tumours
- •15.7.2.4 Calcification in/of Bladder
- •15.7.2.5 Ureterocele
- •15.7.2.6 Persisting Urachus
- •15.7.2.7 Megaureter
- •15.7.2.9 Inflammation
- •15.7.2.10 Traumatic Changes
- •15.7.2.11 Vesico-Ureteric Reflux
- •15.7.3 Paravesical Changes
- •15.7.3.1 Abscess Formations
- •15.7.3.3 Cystic Perivesical Structures
- •15.8.1 US Technique
- •15.8.2 Normal Findings
- •15.8.3 Common Pathologic Findings
- •15.8.3.1 Hydrocele
- •15.8.3.2 Undescended Testes
- •15.8.3.3 Varicocele
- •15.8.3.6 Microlithiasis
- •15.8.4 Inflammation—Orchitis, Ependymitis
- •15.8.5 Scrotal Trauma
- •15.8.6 Torsion
- •15.8.6.2 Inguinal Hernia
- •15.8.7 Testicular Tumours
- •15.9 Female Genitals
- •15.9.1 Indications
- •15.9.2 Requisites
- •15.9.3 Transducers
- •15.9.5 Normal Findings
- •15.9.5.1 Sonogenitography
- •15.9.6 Pathologic Findings
- •15.9.6.1 Congenital Malformations
- •Vaginal Atresia
- •Vaginal Fistula
- •Other Vaginal Malformations
- •Vaginal Aplasia
- •Uterine Malformations
- •Ovarian Malformations
- •Cysts
- •Teratoma
- •Other Genital Tumours
- •Rhabdomyosarcoma
- •15.9.6.4 Traumatic Changes
- •Ovarian Torsion
- •Pregnancy
- •16.1 General Remarks
- •16.2 Examination Technique
- •16.2.2 Modified Graf Classification (Rosendahl)
- •16.3 Normal Anatomy
- •16.3.2 Rosendahl Modification
- •16.3.3 Normal Findings During Harcke Investigation
- •16.5 Pathologic Findings
- •16.6.1.1 Capsular Thickening
- •16.6.1.2 Joint Fluid/Effusion
- •16.6.2 Hip Osteoarthritis
- •16.6.4 Perthes Disease
- •17.1.2 Typical Normal Findings
- •17.1.3 Pathologic Findings
- •17.1.3.1 Fracture
- •17.1.3.2 Joint Effusion
- •17.1.3.3 Arthritis
- •17.1.3.4 Trauma
- •17.1.3.5 Cysts
- •17.1.3.6 Inflammation
- •17.1.3.7 Neoplasia
- •17.2 Other Small Part Applications
- •17.2.1 General Remarks
- •17.2.2 Foreign Bodies

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Positioning for DDH Assessment
Different approaches depending on method, most commonly Graf’s technique
is used:
• Graf’s method—baby positioned in lateral decubitus position with slightly bent
hip and inward rotation:
– Specic devices for placing baby and stabilising transducer helpful (to reduce
angulation artefacts).
– Additional stress test for dynamic assessment performed in the same standard
position and section, mandatory in all hips which are not within the physiological range or have a clinical abnormality.
• Similar approach used for femoral head coverage assessment (French approach)
• Dynamic manoeuvre according to Harcke: part of most exams in North America.
– Transverse view in neutral position and with posterior stress.
• Assessment of joint pathology: supine position.
Transducers
High-resolution linear arrays, 18–5MHz (potentially “trapezoid/convex mode”—
phased linear).
Assessment of effusions and pathology in older children: also curved arrays or
phased (“convex mode”) linear arrays, lower frequencies (10–3MHz).
Device Presets
• Hard post-processing with relatively strong contrast/low dB:
– Some prefer grey scale inversion or bicolour mode.
• Image orientation: cranial = right side of monitor image.
– Some turn monitor by 90° to have a somewhat anatomic presentation (up—
cranial) as originally introduced to reect physiological projection similar to
radiograph.
– Some devices allow for ipping the image on display into this above-
mentioned orientation.
• Rarely (not consistent with general recommendations) cranial position dened as
in abdominal US (left upper monitor corner—cranial), e.g. if hip scan performed
after abdominal US.Note that with this orientation the system’s angel measurement software might be confused.
16.2 Examination Technique
16.2.1 Hip US According toGraf
Access from Lateral in Coronal Section
Acquire image in standard plane according to Graf (Fig.16.1):
• Transducer placed over major trochanter in cranio-caudal coronal direction.

16 Neonatal andPaediatric Hip US
Fig. 16.1 Graf standard plane. (a) Schematic drawing of relevant structures, lines and angles for
hip US according to Graf. (b) Typical corresponding US image (standardised projection—upright
position, always projected as right sided)
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• Then carefully move to parallel sections and rotate on acetabular axis without tilting for imaging the standard plane to be used for diagnosis and measurements.
• Structures to identify on adequate view of acetabular mid portion: lower limb of
bony ilium in depth of acetabular fossa representing physis, middle of acetabular
roof with straight iliac bone line and acetabular labrum (three obligatory landmarks); additionally brief overview of entire joint space should be performed.
Dynamic Assessment
Advisable (normal-appearing hips can be mobile due to laxity of joint capsule after
birth—elastic whipping in normal joint):
• Particularly if suspicious ndings on standard section—mandatory dynamic
assessment.
• Push and pull softly on leg for assessment of stability (femoral head stays well
positioned within joint).
• Instability—displacement of femoral head out of (dysplastic) joint fossa (e.g.
OEGUM/DEGUM recommendation—see: www.OEGUM.at/content/
view/506/210 download “Standarddokumentation der Sonograe der
Neugeborenen- und Säuglingshüfte”):
• In displaced or luxated hips: check for repositionability by respective manoeuvres under US surveillance.
Documentation
Two individually acquired images per hip joint in standard plane:
• One of them must contain measurements (see below, Fig.16.2).
In instable hips, a series of images or video clip showing respective changes dur-
ing stress manoeuvres needs to be documented.

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Fig. 16.2 Relevant structures, one image without (a) and one with (b) angle measurements.
Patient identication and side mandatory, (gestational) age helpful. (a) 1 transition zone of osseous
to cartilaginous part, 2 femoral head, 3 fold, 4 capsule, 5 cartilaginous labrum, 6 cartilaginous roof,
7 osseous contour of ilium bone, 8 bony rim. (b) 1 base line, 1a auxiliary line, 2 bony roof line, 3
cartilaginous coverage line, α (between line 1 and 2) 65°, β (between 1 and 3) 59°
G. Schweintzger et al.
16.2.2 Modified Graf Classification (Rosendahl)
Objective: classify hip morphology and stability separately, have simpler grading—
more easily and consistently applicable.
Technique: hip morphology (α-angle) assessed in standard coronal view (Graf)
with centred femoral head:
• If hip decentring, eccentric or dislocated hips (Graf 2c, D, 3, 4): femoral head
relocated by mild traction, then thereafter reassess hip morphology.
• Irreducible hip—morphology assessed with dislocated femoral head.
Note Always additional Barlow manoeuvre to assess for coexisting instability even
in morphologically normal hips.
• Stability classication as above.
16.2.3 Hip US According toHarcke
Objective: classify hip stability.
Technique: infant lying supine, transducer positioned over lateral aspect of hip.
Coronal images with hip neutral and in exion, plus posterior lip view.
Transverse images with hip exed with passive abduction and adduction, fol-
lowed by transverse images with stress to evaluate hip stability.
Images must document ndings and need to be labeled appropriately (Fig.16.3a).

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16 Neonatal andPaediatric Hip US
Fig. 16.3 Harcke hip US (image and image with labels). (a, b) Normal hip: normal position of
femoral head on this transverse view. Notice cup-like appearance formed by metaphysis and
ischium. No change with stress manoeuvre. (c, d) Abnormal hip: transverse view of hip with stress
showing subluxation of femoral head from its normal position and disruption of cup-like conguration. This hip was reducible. Abbreviations: F femoral head, M femoral metaphysic, I ischium, T
triradiate cartilage, Arrow cartilaginous labrum
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16.2.4 Femoral Head Coverage According toMorin
(and Modified Morin-Terjesen)
Assesses degree of lateralisation of femoral head based on Harcke’s coronal exion view.
Two lines drawn paralleling Graf’s baseline:
• One tangent to lateral part of femoral head.
• One tangent to medial junction of head and acetabular fossa.
• Measure distance between medial and iliac lines and between medial and lateral lines.
• Calculate ratio multiplied by 100 = % of femoral head covered by bony
acetabulum.
Modied Morin (Terjesen): instead of iliac line, use line through lateral bony rim
of acetabulum parallel to long axis of transducer measuring “bony rim percentage”,
later named “femoral head coverage”.
16.2.5 3DUS forDDH Assessment
Several attempts to use AI and (semi-)automated 3DUS reconstruction algorithms
for presenting hip in standardised fashion (usually using Graf and Rosendahl
approach) and for (semi-)automated measurements. Not introduced into clinical
practice as yet not reliable.
Advantage: possibly more standardised if acquisition done properly—less
dependent on possible angling and tilting errors
Disadvantage: no dynamic scanning possible at present

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16.2.6 Assessment ofJoint Effusion, Capsular Thickening,
Perthes, Arthritis andOthers
US performed in supine position leaving leg in spontaneous position:
• Support of knees helpful to relax—less painful.
Transducer positioned anteriorly along femoral neck; usually slightly lateral to
course of femoral vessels sagittal and parasagittal sections acquired—cross sections
rarely helpful but can be acquired.
16.3 Normal Anatomy
Femoral head is roundish, in neonates cartilaginous—later central echogenic ossication centre appears, varying size depending on age.
Additionally: ossied femoral neck, border zone between cartilaginous and ossi-
ed parts, joint capsule—tracking from femoral neck to acetabulum.
16.3.1 US Criteria inGraf
• Good denition of bony rim.
• Undisplaced cartilaginous roof triangle.
• Normal position of well-covered femoral head in acetabular fossa.
• Iliac bone seen as straight line with clear border to cartilaginous acetabular
labrum—good osseous denition.
• Bony angle (α) >60°, cartilaginous angle (β) <55° (dened below):
– Values can be present at birth but must be reached by 3 months.
Correct section through joint with sufcient depiction of all three landmarks
Note
mandatory for judging hip maturity and for performing angle measurements—if
section taken angulated or too ventral or dorsal (usually recognisable by bent shape
of iliac line or incorrect/missing identication of bony fossa denition), measurements always wrong and diagnostically useless.
16.3.2 Rosendahl Modification
No essential difference from Graf technique with addition of compulsory stress test
(similar to Graf’s “dynamic examination”).
Angle measurements—measured between three lines.
• First line (baseline) from osseous rim of iliac bone in straight line paralleling
osseous iliac contour (Fig.16.4a).

16 Neonatal andPaediatric Hip US
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a
c
Fig. 16.4 Hip angle measurements and lines (a–d). (a) How the baseline is dened. (b) Denition
of acetabular roof line. (c) Cartilaginous roof line added, with normal angle α and β—not an upright
standard view, increasingly used for practicability and device restrictions; left-hand image is cranial.
(d) Hip US with integrated sonometer software: the software automatically indicates angles (α 54°,
β 78°) and thus hip type (full line) after manual denition of respective lines (immature type II hip,
suboptimal coverage, dynamic assessment shows elastic whipping) not an upright standard view,
increasingly used for practicability and device restrictions; left-hand side on image is cranial
b
d
• Second line (“bony roof line—acetabular roof line”) from inferior rim of iliac
bone as pivot point tangential to bony roof (Fig.16.4b).
• Third line (“cartilage roof line”) from centre of labrum to bony rim, dened as
point where convexity changes into concavity of acetabulum (Fig.16.4c).
Bony angle α: dened between rst and second lines, shows osseous coverage:
• If normal = good (e.g. more than 50%) (Fig.16.4d).
Cartilaginous angle β: measured between rst and third lines, denes site and
conguration of cartilaginous roof:
• If roof at = high β angle—risk of instability (Fig.16.4e).
Note Angle measurements only valid in correctly performed exams.
Small α angle always indicates dysplasia and poor coverage and at least immaturity.

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16.3.3 Normal Findings During Harcke Investigation
• Cartilaginous femoral head positioned in acetabulum as dened by triradiate cartilage centrally and posterior ischium, with femoral metaphysis seen anteriorly.
• No displacement seen with stress—image remains the same, with head centred
in fossa (see Fig.16.3a).
16.3.4 Anatomic Landmarks andNormal Limits forMeasuring
Femoral Coverage
• Lateral part of femoral head, medial junction of head, acetabular fossa.
• Lower normal limits: boys—47%, girls—44%.
16.4 Hip US inOlder Children
Applications and queries: Perthes disease, infection, proximal femoral deciency,
slipped capital femoral epiphysis, trauma, joint effusion.
Normal US ndings:
• Typically longitudinal section, frontal sagittal view.
• Ossied head, neck connected by non-ossied physis—anechoic line.
• Minimal uid within joint space.
• Capsule small, sometimes difcult to delineate.
• Visible contours of acetabulum and femoral head and neck—continuous, without
disruption, smooth and clearly dened surface (Fig.16.5a).
a
c
b
Fig. 16.5 Normal hip (a) in older children—as opposed to hip effusion (b) and septic hip (c). (a)
Normal longitudinal hip US in an older child; normal joint capsule (synovium) appears prominent,
as both layers are collapsed. (b) Simple hip effusion (transient synovitis, extended eld of view):
echo-free uid in widened joint space, thickened capsule. (c) Power Doppler in septic arthritis:
note impressive hypervascularity of thickened synovium, complex uid in widened joint space

16 Neonatal andPaediatric Hip US
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16.5 Pathologic Findings
16.5.1 Developmental Dysplasia oftheHip (DDH)
Criteria vary depending on method applied (Graf, Harcke, adapted Graf, femoral
head coverage, femoral distance).
Remark/Comment: early detection and treatment = only way for non-invasive
management—important to early recognise DDH to avoid long-term sequelae,
immense healthcare costs, individual morbidity, e.g. by repeated surgery. The debate
of role of screening ongoing in Anglo-American literature; in most of middle
Europe some screening established.
Note Hip US for dysplasia—“nal” investigation (if you miss an endangered hip,
the patient will only come back after years or decades when symptomatic)—strict
and consistent adherence to all quality criteria is essential. As with mammography,
clinical investigation and anamnestic data are mandatory part of every examination.
DDH According to Graf
Strict classication that differentiates between immaturity, dysplasia, instability and
luxation (Table 16.1).
Normal Hip—Type I (described above—“normal ndings”, Figs. 16.1, 16.2,
and 16.4).
Immaturity—Type II
Consider age: depending on subtype, dened by sufcient to poor ossication,
with some rounding of bony rim:
Table 16.1 The Sonometer is a pratical tool for hip classiction, sometimes this or similar graphs
are implemented in US device. A line is drawn betwen the measured alphga and beta angles and
thus the respective hip type (according the Graf classication) is quickly and easily depcitable

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• Cartilaginous acetabulum usually still covering hip but much wider than osseous
acetabulum:
– Due to ossication decit—covering >half of femoral head.
• Potentially delayed ossication.
Subtypes:
• II a +: physiologic immaturity.
• II a–: maturation decit during rst 3 months.
• II b: after third month of life, α≤60°.
• II c: developmentally dysplastic hip—denitely endangered, needs treatment:
– Dynamic stress manoeuvres are mandatory.
• D (IId)—usually unstable hip with beginning decentring:
– Dynamic stress manoeuvres mandatory.
– Very rounded bony rim.
– Initially displaced cartilaginous acetabulum.
– α = 43°–49°, β > 77°.
– Only treatment option = xation.
Decentred Hip: Type III (Fig.16.6)
US Criteria
Femoral head has pushed cartilaginous acetabular roof cranially:
• Insufcient osseous containment with at bony rim.
• Insufcient bony as well as cartilaginous coverage.
• Decentering of femoral head and cartilaginous acetabulum:
• Type III A—hyaline cartilage hypoechoic.
ab
Fig. 16.6 Pathological hips (Graf classication). (a) Immature hip, slightly rounded roof (>3
months of age—type IIa). (b) Endangered hip: severely rounded bony roof, displaced cartilaginous
roof, dynamic assessment mandatory (type D). (c) Dysplastic—decentred hip with at bony
roof—type III. (d) Luxated hip—by denition cartilaginous labrum compressed between femoral
head and iliac bone (type IV)

16 Neonatal andPaediatric Hip US
481
• Type III B—cartilaginous acetabulum small, compressed, distorted + structural
anomalies + some echoes and inhomogeneous. Only in untreated and chronically
dislocated hips − sign of severe damage (remark: very uncommon in Middle
Europe).
• Therapy: needs repositioning and xation.
Luxated Hip: Type IV (Fig.16.6).
US criteria:
• Femoral head displaced from joint space:
• Luxated in cranial, lateral or dorsal position.
• Cartilaginous acetabulum herniated and displaced caudally:
• Pressed in between femoral head and iliac bone—increased inhomogeneous echoes.
• Sometimes difcult to nd bony rim—reliable measurements often impossible/
not required.
• Dynamic assessment helps to evaluate for repositionability.
Note: wrong angulation will cause wrong results—dedicated instruments are
available to reduce probability of this common pitfall (Fig.16.7)
Results in Rosendahl Modification
According to morphology (using Graf angle discrimination):
• Immature, mildly dysplastic, severely dysplastic.
Using stability: stable, dislocatable, dislocated.
DDH According to Harcke
• Classication: normal, lax with stress, subluxed or dislocated (see Fig.16.3b).
Method more subjective; also includes description of hip stability. Neither
Note
accuracy nor population-based rates of pathological hips based on this technique
have been published.
Hip Assessment Based on Femoral Head Coverage
• All outside accepted limits = DDH—less potential for grading, used as initial
screening tools to assess for normal or abnormal hips.
• In abnormal hips, either Harcke or Graf method can be applied additionally for
treatment decisions.
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