Bone Tumors von M. C. Beachley | ISBN 9783540083122

Bone Tumors

von M. C. Beachley und weiteren
Mitwirkende
Autor / AutorinM. C. Beachley
RedaktionK. Ranninger
Autor / AutorinM. H. Becker
Autor / AutorinP. A. Collins
Autor / AutorinK. Doi
Autor / AutorinH. F. Faunce
Autor / AutorinF. Feldman
Autor / AutorinH. Firooznia
Autor / AutorinE. W. Fordham
Autor / AutorinH. Genant
Autor / AutorinN. B. Genieser
Autor / AutorinA. Goldman
Autor / AutorinG. B. Greenfield
Autor / AutorinH. J. Griffith
Autor / AutorinJ. P. Petasnick
Autor / AutorinP. H. Pevsner
Autor / AutorinR. S. Pinto
Autor / AutorinE. W. Ramachandran
Autor / AutorinK. Ranniger
Autor / AutorinF. Schajowicz
Autor / AutorinI. Yaghmai
Buchcover Bone Tumors | M. C. Beachley | EAN 9783540083122 | ISBN 3-540-08312-X | ISBN 978-3-540-08312-2

Bone Tumors

von M. C. Beachley und weiteren
Mitwirkende
Autor / AutorinM. C. Beachley
RedaktionK. Ranninger
Autor / AutorinM. H. Becker
Autor / AutorinP. A. Collins
Autor / AutorinK. Doi
Autor / AutorinH. F. Faunce
Autor / AutorinF. Feldman
Autor / AutorinH. Firooznia
Autor / AutorinE. W. Fordham
Autor / AutorinH. Genant
Autor / AutorinN. B. Genieser
Autor / AutorinA. Goldman
Autor / AutorinG. B. Greenfield
Autor / AutorinH. J. Griffith
Autor / AutorinJ. P. Petasnick
Autor / AutorinP. H. Pevsner
Autor / AutorinR. S. Pinto
Autor / AutorinE. W. Ramachandran
Autor / AutorinK. Ranniger
Autor / AutorinF. Schajowicz
Autor / AutorinI. Yaghmai

Inhaltsverzeichnis

  • Diagnosis, Classification, and Nomenclature of Bone Tumors..
  • A. Introduction.
  • B. Diagnosis of Bone Tumors.
  • C. Radiologic Examination.
  • D. Pathologic Examination.
  • I. Surgical Biopsy.
  • II. Needle or Aspiration Biopsy.
  • E. Value and Limitations of Histochemistry in the Study of Bone Tumors.
  • F. Electron Microscopy.
  • G. Classification and Nomenclature of Bone Tumors.
  • H. Histological Typing of Primary Bone Tumors and Tumorlike Lesions (WHO).
  • References.
  • Radiologie Approach to Bone Tumors..
  • A. Location.
  • B. Cortex.
  • C. The Periosteum.
  • D. Destruction of Bone.
  • E. Margination or Zone of Transition.
  • F. Increase in Bone Density.
  • G. Matrix Calcification.
  • H. Expansion of the Cortex.
  • I. Trabeculation.
  • J. Size.
  • K. Shape.
  • L. The Joint Space.
  • M. The Age of the Patient.
  • N. The Incidence of the Various Tumors.
  • References see page 67.
  • General Concepts and Pathology of Tumors of Osseous Origin..
  • I. Osteoma.
  • II. Osteoid Osteoma.
  • III. Benign Osteoblastoma.
  • IV. Osteogenic Sarcoma or Osteosarcoma.
  • A. Benign Tumors of Osseous Origin.
  • III. Osteoblastoma.
  • B. Malignant Tumors of Osseous Origin.
  • I. Osteogenic Sarcoma (Osteosarcoma, Central Osteosarcoma).
  • II. Primary Multicentric Osteogenic Sarcoma.
  • III. Osteogenic Sarcoma Developing in Abnormal Bone.
  • IV. Osteogenic Sarcoma as a Complication of Paget’s Disease.
  • V. Osteogenic Sarcoma Arising in Previously Irradiated Bone.
  • VI. Osteogenic Sarcoma Associated with Fibrous Dysplasia.
  • VII. Osteogenic Sarcoma in Osteogenesis Imperfecta.
  • VIII. Soft Tissue Osteogenic Sarcoma.
  • Parosteal Osteosarcoma..
  • A. Clinical Features.
  • I. Age and Sex.
  • II. Localization.
  • III. Symptoms.
  • IV. Roentgenographic Features.
  • V. Angiographic Features.
  • VI. Differential Diagnosis.
  • VII. Histopathological Features.
  • B. Treatment.
  • Cartilaginous Tumors and Cartilage-Forming Tumor-like Conditions of the Bones and Soft Tissues..
  • B. Solitary Osteochondroma.
  • I. Pathogenesis.
  • II. Site.
  • III. Clinical.
  • IV. Roentgen.
  • V. Histology.
  • 1. Gross.
  • 2. Microscopic.
  • C. Radiation-Induced Osteochondromas.
  • D. Multiple Osteochondromatosis.
  • I. Clinical.
  • II. Roentgen Features.
  • III. Course.
  • E. Solitary Enchondromas.
  • III. Clinical Features.
  • IV. Roentgen Features.
  • V. Differential Diagnosis.
  • VI. Histology.
  • VII. Treatment and Course.
  • F. Multiple Enchondromatosis.
  • II. Clinical.
  • III. Roentgen Features.
  • IV. Histology.
  • G. Dysplasia Epiphysealis Hemimelica.
  • VI. Course.
  • H. Juxtacortical (periosteal) Chondroma.
  • II. Roentgen.
  • III. Differential Diagnosis.
  • V. Course.
  • I. Chondroblastoma.
  • II. Prevalence and Site.
  • III. Age and Sex Distribution.
  • IV. Symptoms.
  • V. Roentgen Findings in Chondroblastoma.
  • VII. Pathologic Findings.
  • 1. Gross Features.
  • 3. Electron Microscopic Findings.
  • VIII. Treatment and Results.
  • J. Chondromyxoid Fibroma.
  • II. Clinical Features.
  • III. Sites of Localization.
  • VI. Pathologic Findings.
  • VII. Treatment, Recurrence, Malignant Transformation.
  • K. Chondrosarcoma.
  • I. Incidence.
  • II. Age and Sex.
  • IV. Sites.
  • V. Roentgenographic Features.
  • L. Peripheral Chondrosarcoma.
  • I. Histologic Criteria.
  • II. Clinical Course.
  • M. Mesenchymal Chondrosarcoma.
  • II. Course.
  • III. Histology.
  • N. Dedifferentiation of Chondrosarcoma.
  • II. Pathology.
  • 1. Microscopic.
  • III. Roentgen.
  • IV. Course.
  • O. Extraskeletal Cartilage Tumors of the Soft Tissues.
  • I. Malignant Soft Tissue Cartilage Tumors.
  • IV. Treatment and Prognosis.
  • V. Benign Soft Tissue Cartilage Tumors.
  • VI. Pathogenesis.
  • VII. Clinical.
  • VIII. Site.
  • IX. Pathology.
  • X. Roentgen.
  • P. Synovial Chondromatosis.
  • V. Synovial Chondrosarcoma.
  • Q. Summary.
  • Giant Cell Tumor of Bone..
  • B. Pathologic Features.
  • C. Roentgenographic Features.
  • D. Treatment and Prognosis.
  • Marrow Tumors..
  • A. Ewing’s Sarcoma.
  • I. Introduction.
  • II. Incidence.
  • III. Age.
  • IV. Sex Incidence.
  • V. Bones Involved.
  • VI. Clinical Presentation.
  • VII. Laboratory Data.
  • VIII. Radiologic Features.
  • 1. Periosteal Reaction.
  • a) Onion-Skin Pattern of Subperiosteal Bone Formation.
  • b) Right-Angled Spiculation (Sunray Appearance).
  • c) Codman’s triangle.
  • 2. Destruction of Bone.
  • 3. Reactive New Bone Formation.
  • 4. Soft-tissue Swelling.
  • 5. Pathologic Fractures.
  • 6. Other Appearances.
  • 1. Gross •.
  • X. Treatment.
  • XI. Prognosis.
  • XII. Differential Diagnosis.
  • B. Reticulum Cell Sarcoma of Bone.
  • II. History.
  • III. Incidence.
  • IV. Age.
  • V. Sex Incidence.
  • VI. Bones Involved.
  • VII. Clinically.
  • VIII. Laboratory Data.
  • IX. Radiologic Features.
  • 1. Location of Tumor in Bone.
  • 2. Destruction of Cancellous Bone.
  • 3. Destruction of Cortical Bone.
  • 4. Reactive Proliferation of Bone.
  • 5. Cortical Thickening.
  • 6. Periosteal Reaction.
  • 7. Soft-Tissue Involvement.
  • 8. Pathologic Fracture.
  • X. Pathology.
  • XI. Treatment.
  • XII. 5-Year Survival Rate.
  • XIII. Metastases.
  • XIV. Differential Diagnosis.
  • C. Multiple Myeloma and Solitary Plasmacytoma.
  • I. Incidence and Pathogenesis.
  • II. Age.
  • III. Sex.
  • IV. Bones Involved.
  • V. Clinical and Laboratory Data.
  • VI. Diagnosis and Classification.
  • VII. Radiologic Features.
  • 1. Destructive Osteoclastic Lesions.
  • a) Sharply Defined “Punched Out” Lesions.
  • b) Expansile Lytic Areas.
  • c) Generalized Osteoporosis.
  • d) Pathologic Fractures.
  • 2. Mixed Osteolytic and Osteoblastic Lesions.
  • 3. Purely Osteoblastic Lesions.
  • 4. Other Radiologie Features.
  • VIII. Pathology.
  • IX. Treatment.
  • X. Prognosis.
  • 1. Renal Disease in Multiple Myeloma.
  • 2. Amyloid.
  • XI. Differential Diagnosis.
  • D. Lymphoma of Bone.
  • IV. Sex.
  • VIII. Radiologie Features.
  • 1. Lymphosarcoma.
  • 2. Hodgkin’s Disease.
  • IX. Pathologic Features.
  • Vascular Tumors of Bone..
  • A. Hemangiomas.
  • Roentgenographic Appearance.
  • I. Diffuse Skeletal Hemangiomatosis.
  • II. Massive Osteolysis.
  • B. Lymphangioma.
  • C. Glomus Tumor.
  • D. Hemangiopericytoma.
  • E. Hemangioendothelioma (Angiosarcoma).
  • Connective Tissue Tumors of Bone..
  • A. Chondrogenic Series.
  • B. Fibrogenic Series.
  • C. Fibrosarcoma.
  • D. Lipoma.
  • E. Liposarcoma.
  • Chordoma..
  • B. Embryology.
  • I. General Considerations.
  • II. Formation of Notochord.
  • III. Origin of Notochord.
  • IV. Chordal Ectopia and Chordal Remnants.
  • 1. Ecchordosis Physaliphora.
  • 2. Other Notochordal Remnants.
  • 3. Relationship of Notochordal Remnants to Chordoma.
  • C. Pathology.
  • I. Gross Pathology.
  • 1. General Considerations.
  • 2. Classification of Chordoma.
  • 3. Topographic Distribution of Chordoma.
  • 4. Gross Pathology of the Intracranial Chordomas.
  • 5. Gross Pathology of Nasopharyngeal Chordomas.
  • 6. Gross Pathology of Vertebral Chordomas.
  • 7. Gross Pathology of Sacrococcygeal Chordomas.
  • 8. Histology of Chordoma.
  • a) Histogenesis.
  • b) Cytology.
  • 9. Metastasis.
  • 10. Chordoma in Unusual Locations.
  • D. Clinical Findings.
  • 1. Age and Sex.
  • 2. Symptomatology.
  • a) Clinical Findings in Intracranial Chordomas.
  • b) Clinical Findings in Nasopharyngeal Chordoma.
  • c) Clinical Findings in Vertebral Chordoma.
  • d) Clinical Findings in Sacrococcygeal Chordoma.
  • E. Roentgenologic Findings.
  • I. Intracranial Chordomas.
  • 1. Plain Film Findings (Including Body-Section Radiography).
  • 2. Calcifications.
  • 3. Angiography.
  • a) Carotid Angiography.
  • b) Vertebral Angiography.
  • 4. Pneumoencephalography.
  • 5. Brain Scan (Technetium 99m pertechnetate).
  • 6. Computerized Tomographic (CT) Scan.
  • II. Nasopharyngeal Chordomas.
  • III. Vertebral Chordomas.
  • 1. Plain Film Findings.
  • 2. Myelography.
  • IV. Sacrococcygeal Chordoma.
  • V. Diagnosis.
  • VI. Treatment.
  • Adamantinoma (Malignant Angioblastoma), Schwannoma (Neurilemmoma), Neurofibroma..
  • A. Adamantinoma Long Bones and Ameloblastoma — Jaw.
  • I. Nomenclature.
  • III. Pathology.
  • IV. Roentgenology.
  • V. Treatment.
  • B. Schwannoma (Neurilemmoma).
  • C. Neurofibroma.
  • Tumor-like Lesions..
  • A. The Solitary Bone Cyst.
  • IV. Pathology.
  • V. Pathogenesis.
  • VI. Roentgenology.
  • VII. Differential Diagnosis.
  • VIII. Treatment and Prognosis.
  • B. Aneurysmal Bone Cyst.
  • C. Juxta-Articular Bone Cyst (Intraosseous Ganglia).
  • II. Etiology.
  • V. Roentgen Appearance.
  • D. The Fibrous Cortical Defect or Nonosteogenic Fibroma.
  • III. Clinical Manifestations.
  • 1. Laboratory Findings.
  • 2. Other Clinical Findings.
  • IV. Location and Bilaterality.
  • VI. Pathology.
  • VII. Roentgenology.
  • VIII. Roentgenologic Course and Prognosis.
  • IX. Differential Diagnosis.
  • E. Eosinophilic Granuloma.
  • IV. Pathogenesis.
  • V. Radiographic Findings.
  • 1. Skull.
  • 2. Mandible.
  • 3. Spine.
  • 4. Long and Flat Bones.
  • VIII. Treatment and Course.
  • F. Fibrous Dysplasia.
  • 1. Monostotic Fibrous Dysplasia.
  • 2. Polyostotic Fibrous Dysplasia and Albright Syndrome.
  • 3. Associated Disorders.
  • 4. Malignant Transformation.
  • V. Etiology.
  • VIII. Treatment.
  • G. Myositis Ossificans.
  • 1. Other Terms.
  • 2. Etiology.
  • 3. Clinical.
  • 4. Pathology.
  • 5. Roentgen Appearance.
  • 6. Treatment.
  • II. Myositis Ossificans Progressiva.
  • H. Brown Tumors of Hyperparathyroidism.
  • III. Etiology.
  • 1. Primary Hyperparathyroidism.
  • 2. Secondary Hyperparathyroidism.
  • IV. Clinical.
  • V. Pathology.
  • VI. Roentgen Findings.
  • Metastatic Bone Disease..
  • A. Incidence.
  • B. Localization.
  • C. Method of Diagnosis.
  • I. Clinical Evaluation.
  • II. Roentgenographic Examination.
  • III. Bone Scanning.
  • D. Mechanisms of Metastasis.
  • E. Roentgenographic Diagnosis.
  • I. Patterns of Destruction.
  • II. Osteolytic Metastases.
  • III. Osteoblastic Metastases.
  • IV. Periosteal New Bone Formation.
  • V. Roentgenographic Characteristics.
  • VI. Spinal Metastases.
  • VII. Rib Metastases.
  • VIII. Skull Metastases.
  • IX. Peripheral Metastases.
  • X. Metastatic Disease in Children.
  • Conclusion.
  • Study of Bone Tumors with Radionuclides..
  • A. Radionuclides.
  • I. Isotopes of Calcium.
  • II. Isotopes of Strontium.
  • III. Fluorine-18.
  • IV. Miscellaneous Radionuclides.
  • V. 99mTc Labeled Phosphate Compounds.
  • VI. Bone Marrow Imaging Agents.
  • B. Instrumentation.
  • C. Mechanisms of Localization.
  • D. Indications for Radionuclide Imaging of the Skeleton.
  • E. Malignant Tumors.
  • I. Osteosarcoma.
  • II. Malignant Tumors of Cartilaginous Origin.
  • III. Malignant Tumors of Vascular and Connective Tissue Origin.
  • IV. Malignant Tumors of Marrow Origin.
  • 1. Ewing’s Sarcoma.
  • 2. Myeloma.
  • 3. Leukemia.
  • 4. Lymphoma.
  • F. Benign Tumors and Tumorlike Abnormalities.
  • 1. Osteoid Osteoma and Osteoblastoma.
  • 2. Chondroma.
  • 3. Giant Cell Tumor.
  • 4. Aneurysmal Bone Cyst.
  • 5. Fibrous Dysplasia.
  • 6. Paget’s Disease.
  • 7. Eosinophilic Granuloma.
  • 8. Miscellaneous Lesions.
  • G. Conclusion.
  • Angiography of Bone Tumors..
  • B. Vascular Anatomy.
  • I. Nutrient Arteries.
  • II. Periosteal and Perichondral Arteries.
  • III. Metaphyseal and Epiphyseal Arteries.
  • IV. Arterial Supply of Bone Lesions.
  • C. Arteriography.
  • I. Technique.
  • II. Pharmacoangiography.
  • III. Subtraction.
  • IV. Complications.
  • V. General Roentgenographic Findings.
  • D. Bone-Forming Tumors.
  • IV. Osteosarcoma.
  • V. Parosteal Osteosarcoma (Juxtacortical Osteosarcoma).
  • E. Cartilage-Forming Tumors.
  • I. Chondroma.
  • II. Osteochondroma.
  • III. Chondromyxoid Fibroma ..
  • IV. Benign Chondroblastoma.
  • V. Chondrosarcoma.
  • VI. Mesenchymal Chondrosarcoma.
  • F. Giant Cell Tumor and Aneurysmal Bone Cyst.
  • G. Vascular Tumors.
  • I. Hemangioma.
  • II. Lymphangioma.
  • III. Hemangiopericytoma.
  • H. Other Connective Tissue Tumors.
  • I. Lipoma.
  • II. Desmoplastic Fibroma.
  • III. Fibrosarcoma.
  • IV. Liposarcoma.
  • I. Marrow Tumors.
  • I. Ewing’s Sarcoma and Reticulum Cell Sarcoma.
  • II. Myeloma.
  • J. Other Tumors.
  • I. Chordoma.
  • II. Adamantinoma of Long Bone.
  • III. Neurolemmoma (Schwannoma, Neuronoma).
  • K. Tumorlike Lesions.
  • I. Metaphyseal Fibrous Defect (Nonossifying Fibroma).
  • II. Fibrous Dysplasia.
  • III. Myositis Ossifìcans.
  • L. Metastatic Bone Lesions.
  • I. Osteolytic Metastasis.
  • II. Osteoblastic Metastasis.
  • High-Resolution Radiographic Techniques for the Detection and Study of Skeletal Neoplasms..
  • A. Radiographic Techniques.
  • B. Comparison of Images Using Magnification Techniques.
  • I. Optical Magnification.
  • II. Optical Vs. Radiographic Magnification.
  • III. Radiographic Magnification.
  • Summary and Conclusions.
  • Author Index — Namenverzeichnis.