The Netter Collection of Medical Illustrations: Musculoskeletal System, Volume 6, Part III - Biology and Systemic Diseases

Herausgeber: Iannotti, Joseph; Abelson, Abby; Patterson, Brendan; Mroz, Tom; Parker, Richard

• Gebundenes Buch

Produktbeschreibung

Offering a concise, highly visual approach to the basic science and clinical pathology of the musculoskeletal system, this updated volume in The Netter Collection of Medical Illustrations (the CIBA "Green Books") contains unparalleled didactic illustrations reflecting the latest medical knowledge. Revised by Drs. Joseph Iannotti, Richard Parker, Abby G. Abelson, Brendan M. Patterson, and other experts from the Cleveland Clinic, Biology and Systemic Diseases, Part 3 of Musculoskeletal System, Volume 6, integrates core concepts of anatomy, physiology, and other basic sciences with common clinical correlates across health, medical, and surgical disciplines. Classic Netter art, updated and new illustrations, and modern imaging continue to bring medical concepts to life and make this timeless work an essential resource for students, clinicians, and educators. * Provides a highly visual guide to embryology and physiology, metabolic disorders, congenital and development disorders, rheumatic diseases, tumors of the musculoskeletal system, injury to the musculoskeletal system, soft tissue infections, and fracture complications. * Provides a concise overview of complex information by seamlessly integrating anatomical and physiological concepts using practical clinical scenarios. * Shares the experience and knowledge of Drs. Joseph P. Iannotti, Richard D. Parker, Abby G. Abelson, and Brendan M. Patterson, and esteemed colleagues from the Cleveland Clinic, who clarify and expand on the illustrated concepts. * Compiles Dr. Frank H. Netter’s master medical artistry-an aesthetic tribute and source of inspiration for medical professionals for over half a century-along with new art in the Netter tradition for each of the major body systems, making this volume a powerful and memorable tool for building foundational knowledge and educating patients or staff. * NEW! An eBook version is included with purchase. The eBook allows you to access all of the text, figures, and references, with the ability to search, make notes and highlights, and have content read aloud.

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Produktdetails

• Netter Green Book Collection
• Verlag: Elsevier - Health Sciences Division
• 3 ed
• Seitenzahl: 368
• Erscheinungstermin: 19. März 2024
• Englisch
• Abmessung: 300mm x 247mm x 21mm
• Gewicht: 1406g
• ISBN-13: 9780323880879
• ISBN-10: 0323880878
• Artikelnr.: 69877075

Inhaltsangabe

SECTION 1 EMBRYOLOGY 1.1 Amphioxus and Human Embryo at 16 Days 1.2
Differentiation of Somites into Myotomes, Sclerotomes, and Dermatomes 1.3
Progressive Stages in Formation of Vertebral Column, Dermatomes, and
Myotomes; Mesenchymal Precartilage Primordia of Axial and Appendicular
Skeletons at 5 Weeks 1.4 Fate of Body, Costal Process, and Neural Arch
Components of Vertebral Column, with Sites and Time of Appearance of
Ossification Centers 1.5 First and Second Cervical Vertebrae at Birth;
Development of Sternum 1.6 Early Development of Skull 1.7 Skeleton of
Full-Term Newborn 1.8 Changes in Position of Limbs Before Birth;
Precartilage Mesenchymal Cell Concentrations of Appendicular Skeleton at 6
Weeks 1.9 Changes in Ventral Dermatome Pattern During Limb Development 1.10
Initial Bone Formation in Mesenchyme; Early Stages of Flat Bone Formation
1.11 Secondary Osteon (Haversian System) 1.12 Growth and Ossification of
Long Bones 1.13 Growth in Width of a Bone and Osteon Remodeling 1.14
Remodeling: Maintenance of Basic Form and Proportions of Bone during Growth
1.15 Development of Three Types of Synovial Joints 1.16 Segmental
Distribution of Myotomes in Fetus of 6 Weeks; Developing Skeletal Muscles
at 8 Weeks 1.17 Development of Skeletal Muscle Fibers 1.18 Cross Sections
of Body at 6 to 7 Weeks 1.19 Prenatal Development of Perineal Musculature
1.20 Origins and Innervations of Pharyngeal Arch and Somite Myotome Muscles
1.21 Branchiomeric and Adjacent Myotomic Muscles at Birth SECTION
2 PHYSIOLOGY 2.1 Microscopic Appearance of Skeletal Muscle Fibers 2.2
Organization of Skeletal Muscle 2.3 Intrinsic Blood and Nerve Supply of
Skeletal Muscle 2.4 Composition and Structure of Myofilaments 2.5 Muscle
Contraction and Relaxation 2.6 Biochemical Mechanics of Muscle Contraction
2.7 Sarcoplasmic Reticulum and Initiation of Muscle Contraction 2.8
Initiation of Muscle Contraction by Electric Impulse and Calcium Movement
2.9 Motor Unit 2.10 Structure of Neuromuscular Junction 2.11 Physiology of
Neuromuscular Junction 2.12 Pharmacology of Neuromuscular Transmission 2.13
Physiology of Muscle Contraction 2.14 Energy Metabolism of Muscle 2.15
Muscle Fiber Types 2.16 Growth Plate: Structure, Physiology, and
Pathophysiology 2.17 Growth Plate: Structure, Physiology, and
Pathophysiology (Continued) 2.18 Growth Plate: Structure and Blood Supply
2.19 Growth Plate: Peripheral Fibrocartilaginous Element 2.20 Composition
and Structure of Cartilage 2.21 Bone Cells and Bone Deposition 2.22
Composition of Bone 2.23 Structure of Cortical (Compact) Bone 2.24
Structure of Trabecular Bone 2.25 Formation and Composition of Collagen
2.26 Formation and Composition of Proteoglycan 2.27 Structure and Function
of Synovial Membrane 2.28 Histology of Connective Tissue 2.29 Bone
Homeostasis: Dynamics 2.30 Bone Homeostasis: Regulation of Calcium and
Phosphate Metabolism 2.31 Effects of Bone Formation and Bone Resorption on
Skeletal Mass 2.32 Four Mechanisms of Bone Mass Regulation 2.33 Normal
Calcium and Phosphate Metabolism 2.34 Nutritional Calcium Deficiency 2.35
Effects of Disuse and Stress (Weight Bearing) on Bone Mass 2.36
Musculoskeletal Effects of Weightlessness (Space Flight) 2.37 Bone
Architecture and Remodeling in Relation to Stress 2.38 Stress-Generated
Electric Potentials in Bone 2.39 Bioelectric Potentials in Bone 2.40
Age-Related Changes in Bone Geometry 2.41 Age-Related Changes in Bone
Geometry (Continued) SECTION 3 METABOLIC DISEASES 3.1 Parathyroid Hormone
3.2 Primary Hyperparathyroidism: Pathophysiology 3.3 Primary
Hyperparathyroidism: Clinical Manifestations 3.4 Differential Diagnosis of
Hypercalcemic States 3.5 Hypoparathyroidism: Pathologic Physiology 3.6
Chronic Hypoparathyroidism: Clinical Manifestations 3.7 Hypocalcemia:
Clinical Manifestations 3.8 Pseudohypoparathyroidism 3.9 Mechanism of
Parathyroid Hormone Activity on End Organ 3.10 Mechanism of Parathyroid
Hormone Activity on End Organ: Cyclic AMP Response to PTH 3.11 Clinical
Guide to Parathyroid Hormone Assay 3.12 Clinical Guide to Parathyroid
Hormone Assay (Continued) 3.13 Childhood Rickets 3.14 Adult Osteomalacia
3.15 Nutritional Deficiency: Rickets and Osteomalacia 3.16 Vitamin
D-Resistant Rickets and Osteomalacia Due to Proximal Renal Tubular Defects
(Hypophosphatemic Rachitic Syndromes) 3.17 Vitamin D-Resistant Rickets and
Osteomalacia Due to Proximal and Distal Renal Tubular Defects 3.18 Vitamin
D-Dependent (Pseudodeficiency) Rickets and Osteomalacia 3.19 Vitamin
D-Resistant Rickets and Osteomalacia Due to Renal Tubular Acidosis 3.20
Metabolic Aberrations of Renal Osteodystrophy 3.21 Rickets, Osteomalacia,
and Renal Osteodystrophy 3.22 Bony Manifestations of Renal Osteodystrophy
3.23 Vascular and Soft Tissue Calcification in Secondary
Hyperparathyroidism of Chronic Renal Disease 3.24 Clinical Guide to Vitamin
D Measurement 3.25 Hypophosphatasia 3.26 Osteoporosis: Risk Factors 3.27
Osteoporosis: Involutional 3.28 Osteoporosis: Clinical Manifestations 3.29
Osteoporosis: Progressive Spinal Deformity 3.30 Radiology of Osteopenia:
Classification 3.31 Radiology of Osteopenia: Imaging 3.32 Radiology of
Osteopenia: DXA 3.33 Transiliac Bone Biopsy 3.34 Treatment of Complications
of Spinal Osteoporosis 3.35 Treatment of Osteoporosis: Medications 3.36
Treatment of Osteoporosis: Functional Domains of Bisphosphonate Chemical
Structure 3.37 Treatment of Osteoporosis: Inhibition of FPP Synthase 3.38
Osteogenesis Imperfecta Type I 3.39 Osteogenesis Imperfecta Type III 3.40
Marfan Syndrome 3.41 Marfan Syndrome (Continued) 3.42 Ehlers-Danlos
Syndromes 3.43 Ehlers-Danlos Syndromes (Continued) 3.44 Osteopetrosis
(Albers-Schönberg Disease) 3.45 Paget Disease of Bone 3.46 Paget Disease of
Bone (Continued) 3.47 Pathophysiology and Treatment of Paget Disease of
Bone 3.48 Fibrodysplasia Ossificans Progressiva SECTION 4 CONGENITAL AND
DEVELOPMENTAL DISORDERS Dwarfism 4.1 Achondroplasia: Clinical
Manifestations 4.2 Achondroplasia: Clinical Manifestations (Continued) 4.3
Achondroplasia: Clinical Manifestations of Spine 4.4 Achondroplasia:
Diagnostic Testing 4.5 Hypochondroplasia 4.6 Diastrophic Dwarfism 4.7
Pseudoachondroplasia 4.8 Metaphyseal Chondrodysplasia, McKusick Type 4.9
Metaphyseal Chondrodysplasia, Schmid Type 4.10 Chondrodysplasia Punctata
4.11 Chondroectodermal Dysplasia (Ellis-van Creveld Syndrome), Grebe
Chondrodysplasia, and Acromesomelic Dysplasia 4.12 Multiple Epiphyseal
Dysplasia, Fairbank Type 4.13 Pycnodysostosis (Pyknodysostosis) 4.14
Camptomelic (Campomelic) Dysplasia 4.15 Spondyloepiphyseal Dysplasia Tarda
and Spondyloepiphyseal Dysplasia Congenita 4.16 Spondylocostal Dysostosis
and Dyggve-MelchiorClausen Dysplasia 4.17 Kniest Dysplasia 4.18
Mucopolysaccharidoses 4.19 Principles of Treatment of Skeletal Dysplasias
Neurofibromatosis 4.20 Diagnostic Criteria and Cutaneous Lesions in
Neurofibromatosis 4.21 Cutaneous Lesions in Neurofibromatosis 4.22 Spinal
Deformities in Neurofibromatosis 4.23 Bone Overgrowth and Erosion in
Neurofibromatosis Other 4.24 Arthrogryposis Multiplex Congenita 4.25
Fibrodysplasia Ossificans Progressiva and Progressive Diaphyseal Dysplasia
4.26 Osteopetrosis and Osteopoikilosis 4.27 Melorheostosis 4.28 Congenital
Elevation of Scapula, Absence of Clavicle, and Pseudarthrosis of Clavicle
4.29 Madelung Deformity 4.30 Congenital Bowing of the Tibia 4.31 Congenital
Pseudoarthrosis of the Tibia and Dislocation of the Knee Leg-Length
Discrepancy 4.32 Clinical Manifestations 4.33 Evaluation of Leg-Length
Discrepancy 4.34 Charts for Timing Growth Arrest and Determining Amount of
Limb Lengthening to Achieve Limb-Length Equality at Maturity 4.35 Growth
Arrest 4.36 Ilizarov and De Bastiani Techniques for Limb Lengthening
Congenital Limb Malformation 4.37 Growth Factors 4.38 Foot Prehensility in
Amelia 4.39 Failure of Formation of Parts: Transverse Arrest 4.40 Failure
of Formation of Parts: Transverse Arrest (Continued) 4.41 Failure of
Formation of Parts: Transverse Arrest (Continued) 4.42 Failure of Formation
of Parts: Transverse Arrest (Continued) 4.43 Failure of Formation of Parts:
Transverse Arrest (Continued) 4.44 Failure of Formation of Parts:
Transverse Arrest (Continued) 4.45 Failure of Formation of Parts:
Transverse Arrest (Continued) 4.46 Failure of Formation of Parts:
Longitudinal Arrest 4.47 Failure of Formation of Parts: Longitudinal Arrest
(Continued) 4.48 Failure of Formation of Parts: Longitudinal Arrest
(Continued) 4.49 Failure of Formation of Parts: Longitudinal Arrest
(Continued) 4.50 Duplication of Parts, Overgrowth, and Congenital
Constriction Band Syndrome SECTION 5 RHEUMATIC DISEASES Rheumatic Diseases
5.1 Joint Pathology in Rheumatoid Arthritis 5.2 Early and Moderate Hand
Involvement in Rheumatoid Arthritis 5.3 Advanced Hand Involvement in
Rheumatoid Arthritis 5.4 Foot Involvement in Rheumatoid Arthritis 5.5 Knee,
Shoulder, and Hip Joint Involvement in Rheumatoid Arthritis 5.6
Extraarticular Manifestations in Rheumatoid Arthritis 5.7 Extraarticular
Manifestations in Rheumatoid Arthritis (Continued) 5.8 Immunologic Features
in Rheumatoid Arthritis 5.9 Variable Clinical Course of Adult Rheumatoid
Arthritis Treatment of Rheumatoid Arthritis 5.10 Exercises for Upper
Extremities 5.11 Exercises for Shoulders and Lower Extremities 5.12
Surgical Management in Rheumatoid Arthritis Synovial Fluid Examination 5.13
Techniques for Aspiration of Joint Fluid 5.14 Synovial Fluid Examination
5.15 Synovial Fluid Examination (Continued) Juvenile Arthritis 5.16
Systemic Juvenile Arthritis 5.17 Systemic Juvenile Arthritis (Continued)
5.18 Hand Involvement in Juvenile Arthritis 5.19 Lower Limb Involvement in
Juvenile Arthritis 5.20 Ocular Manifestations in Juvenile Arthritis 5.21
Sequelae of Juvenile Arthritis Osteoarthritis 5.22 Distribution of Joint
Involvement in Osteoarthritis 5.23 Clinical Findings in Osteoarthritis 5.24
Clinical Findings in Osteoarthritis (Continued) 5.25 Hand Involvement in
Osteoarthritis 5.26 Hip Joint Involvement in Osteoarthritis 5.27
Degenerative Changes 5.28 Spine Involvement in Osteoarthritis Other 5.29
Ankylosing Spondylitis 5.30 Ankylosing Spondylitis (Continued) 5.31
Degenerative Changes in the Cervical Vertebrae 5.32 Psoriatic Arthritis
5.33 Psoriatic Arthritis (Continued) 5.34 Reactive Arthritis (formerly
Reiter Syndrome) 5.35 Infectious Arthritis 5.36 Tuberculous Arthritis 5.37
Hemophilic Arthritis 5.38 Neuropathic Joint Disease 5.39 Gout and Gouty
Arthritis 5.40 Tophaceous Gout 5.41 Calcium Pyrophosphate Deposition
Disease (Pseudogout) 5.42 Nonarticular Rheumatism 5.43 Clinical
Manifestations of Polymyalgia Rheumatica and Giant Cell Arteritis 5.44
Imaging of Polymyalgia Rheumatica and Giant Cell Arteritis 5.45
Fibromyalgia 5.46 Pathophysiology of Autoinflammatory Syndromes 5.47
Cutaneous Findings in Autoinflammatory Syndromes 5.48 Joint and Central
Nervous System Findings in Autoinflammatory Syndromes 5.49 Vasculitis:
Vessel Distribution 5.50 Vasculitis: Clinical and Histologic Features of
Granulomatosis with Polyangiitis 5.51 Key Clinical Features of Primary
Vasculitic Diseases 5.52 Renal Lesions in Systemic Lupus Erythematosus 5.53
Cutaneous Lupus Band Test 5.54 Lupus Erythematosus of the Heart 5.55
Antiphospholipid Syndrome 5.56 Scleroderma: Clinical Manifestations 5.57
Scleroderma: Clinical Findings 5.58 Scleroderma: Radiographic Findings of
Acro-osteolysis and Calcinosis Cutis 5.59 Polymyositis and Dermatomyositis
5.60 Polymyositis and Dermatomyositis (Continued) 5.61 Primary Angiitis of
the Central Nervous System 5.62 Behçet Syndrome: Triad 5.63 Behçet
Syndrome: Positive Pathergy Test SECTION 6 TUMORS OF MUSCULOSKELETAL SYSTEM
6.1 Initial Evaluation and Staging of Musculoskeletal Tumors Benign Tumors
of Bone 6.2 Osteoid Osteoma 6.3 Osteoblastoma 6.4 Enchondroma 6.5
Periosteal Chondroma 6.6 Osteocartilaginous Exostosis (Osteochondroma) 6.7
Chondroblastoma and Chondromyxoid Fibroma 6.8 Fibrous Dysplasia 6.9
Nonossifying Fibroma and Desmoplastic Fibroma 6.10 Eosinophilic Granuloma
6.11 Aneurysmal Bone Cyst 6.12 Simple Bone Cyst 6.13 Giant Cell Tumor of
Bone Malignant Tumors of Bone 6.14 Osteosarcoma 6.15 Osteosarcoma
(Continued) 6.16 Osteosarcoma (Continued) 6.17 Chondrosarcoma 6.18 Fibrous
Histiocytoma and Fibrosarcoma of Bone 6.19 Reticuloendothelial Tumors:
Ewing Sarcoma 6.20 Malignant Tumors of Bone: Adamantinoma 6.21 Malignant
Tumors of Bone: Plasmacytoma/Multiple Myeloma 6.22 Tumors Metastatic to
Bone Benign Tumors of Soft Tissue 6.23 Desmoid, Fibromatosis, and
Hemangioma 6.24 Lipoma, Neurofibroma, and Myositis Ossificans Malignant
Tumors of Soft Tissue 6.25 Sarcomas of Soft Tissue 6.26 Sarcomas of Soft
Tissue (Continued) 6.27 Sarcomas of Soft Tissue (Continued) Procedures 6.28
Tumor Biopsy 6.29 Surgical Margins 6.30 Reconstruction after Partial
Excision or Curettage of Bone (Fracture Prophylaxis) 6.31 Limb-Salvage
Procedures for Reconstruction 6.32 Radiologic Findings in Limb-Salvage
Procedures 6.33 Limb-Salvage Procedures SECTION 7 INJURY TO MUSCULOSKELETAL
SYSTEM 7.1 Closed Soft Tissue Injuries 7.2 Open Soft Tissue Wounds 7.3
Treatment of Open Soft Tissue Wounds 7.4 Pressure Ulcers 7.5 Excision of
Deep Pressure Ulcer 7.6 Classification of Burns 7.7 Causes and Clinical
Types of Burns 7.8 Escharotomy for Burns 7.9 Prevention of Infection in
Burn Wounds 7.10 Metabolic and Systemic Effects of Burns 7.11 Excision and
Grafting for Burns 7.12 Etiology of Compartment Syndrome 7.13
Pathophysiology of Compartment and Crush Syndromes 7.14 Acute Anterior
Compartment Syndrome 7.15 Measurement of Intracompartmental Pressure 7.16
Incisions for Compartment Syndrome of Forearm and Hand 7.17 Incisions for
Compartment Syndrome of Leg 7.18 Healing of Incised, Sutured Skin Wound
7.19 Healing of Excised Skin Wound 7.20 Types of Joint Injury 7.21
Classification of Fracture 7.22 Types of Displacement 7.23 Types of
Fracture 7.24 Healing of Fracture 7.25 Primary Union 7.26 Factors That
Promote or Delay Bone Healing SECTION 8 SOFT TISSUE INFECTIONS 8.1 Septic
Joint 8.2 Etiology and Prevalence of Hematogenous Osteomyelitis 8.3
Pathogenesis of Hematogenous Osteomyelitis 8.4 Clinical Manifestations of
Hematogenous Osteomyelitis 8.5 Direct (Nonhematogenous) Causes of
Osteomyelitis 8.6 Direct (Nonhematogenous) Causes of Osteomyelitis
(Continued) 8.7 Osteomyelitis after Open Fracture 8.8 Recurrent
Postoperative Osteomyelitis 8.9 Delayed Posttraumatic Osteomyelitis in
Diabetic Patient SECTION 9 FRACTURE COMPLICATIONS 9.1 Neurovascular Injury
9.2 Acute Respiratory Distress Syndrome 9.3 Infection 9.4 Surgical
Management of Open Fractures 9.5 Gas Gangrene 9.6 Implant Failure 9.7
Malunion of Fracture 9.8 Growth Deformity 9.9 Posttraumatic Osteoarthritis
9.10 Osteonecrosis 9.11 Joint Stiffness 9.12 Complex Regional Pain Syndrome
9.13 Nonunion of Fracture 9.14 Surgical Management of Nonunion 9.15
Electric Stimulation of Bone Growth 9.16 Noninvasive Coupling Methods of
Electric Stimulation of Bone Selected References Index