An edition of Tumors of the Bones and Joints (Atlas of Tumor Pathology Series IV)
(2005)
Tumors of the Bones and Joints (Atlas of Tumor Pathology Series IV)
1 edition
by K. Krishnan Unni
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Tumors of the Bones and Joints (Atlas of Tumor Pathology Series IV)
October 2005, Arp
Hardcover
in English
- 1 edition
188104193X 9781881041931
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Book Details
Table of Contents
1.
Introduction
1.1.
Structure of Normal Bone
1.2.
Development of Bone
1.2.1.
Intramembranous Ossification
1.2.2.
Endochondral Ossification
1.3.
Classification of Bone Tumors
1.4.
Incidence of Bone Tumors
1.5.
Methods of Biopsy
1.5.1.
Open Biopsy
1.5.2.
Needle Biopsy
1.5.3.
Fine-Needle Aspiration Biopsy
1.6.
Handling of Specimens
1.6.1.
Decalcification
1.6.2.
Assessment of Chemotherapy Effect
1.7.
Grading of Bone Tumors
1.8.
Staging of Bone Tumors
2.
Genetics of Bone Tumors
2.1.
Introduction
2.2.
Basic Principles of Cancer Cytogenetics
2.3.
Cytogenic Analysis
2.3.1.
Specimen Requirements
2.3.2.
Cell Culture and Chromosome Banding
2.3.3.
Nomenclature
2.4.
Molecular Cytogenetics
2.4.1.
Specimen
2.4.2.
Probes
2.4.3.
Technical Variations
2.5.
Molecular Biology
2.5.1.
Oncogenes
2.5.2.
Oncogene Detection
2.5.3.
Gene Amplification
2.5.4.
Tumor Suppressor Genes
2.6.
DNA Mismatch Repair Gene Defects
2.6.1.
Microarray Technology
3.
Radiographic Appearance of Bone Tumors
3.1.
Location
3.2.
Size
3.3.
Internal Margins
3.4.
Matrix Pattern
3.5.
Proliferative Bone Induction
3.6.
Interrupted Periosteal Reaction
3.7.
Radionuclide Bone Imaging
3.8.
Computerized Tomograms
3.9.
Magnetic Resonance Imaging
4.
Cartilaginous Lesions
4.1.
Osteochondroma
4.2.
Multiple Hereditary Exostoses
4.3.
Enchondroma
4.4.
Multiple Chondromas
4.5.
Periosteal Chondroma
4.6.
Soft Tissue Chondroma
4.7.
Chondroblastoma
4.8.
Chondromyxoid Fibroma
4.9.
Chondrosarcoma
4.9.1.
Chondrosarcoma of the Small Bones of the Hands and Feet
4.9.2.
Periosteal Chondrosarcoma
4.9.3.
Secondary Chondrosarcoma
4.9.4.
Dedifferentiated Chondrosarcoma
4.9.5.
Mesenchymal Chondrosarcoma
4.9.6.
Clear Cell Chondrosarcoma
5.
Bone-Forming Lesions
5.1.
Benign Bone-Forming Tumors
5.1.1.
Osteoid Osteoma
5.1.2.
Osteoblastoma
5.2.
Malignant Bone-Forming Tumors
5.2.1.
Osteosarcoma of Bone
5.3.
Medullary Osteosarcomas
5.3.1.
Conventional Osteosarcoma
5.3.2.
Osteosarcoma of Jawbones
5.3.3.
Osteosarcoma in Paget's Disease
5.3.4.
Postradiation Sarcoma
5.3.5.
Osteosarcoma in Other Benign Conditions
5.3.6.
Multicentric Osteosarcoma
5.3.7.
Telangiectatic Osteosarcoma
5.3.8.
Small Cell Osteosarcoma
5.3.9.
Low-Grade Osteosarcoma
5.4.
Genetics and Other Special Techniques
5.4.1.
Genetic Predisposition to Osteosarcoma
5.4.2.
Prognostic Markers
5.4.3.
Other Potential Genetic Lesions
5.4.4.
Tumor Cytogenetics
5.5.
Treatment and Prognosis for Patients with Osteosarcomas
5.6.
Osteosarcomas of the Surface of the Bone
5.6.1.
Parosteal Osteosarcoma
5.6.2.
Periosteal Osteosarcoma
5.6.3.
High-Grade Surface Osteosarcoma
6.
Fibrogenic Tumors
6.1.
Desmoplastic Fibroma
6.2.
Fibrosarcoma
7.
"Histiocytic" Tumors
7.1.
Benign Fibrous Histiocytoma
7.2.
Malignant Fibrous Histiocytoma
8.
Small Cell Malignancies
8.1.
Ewing's Sarcoma
8.2.
Myeloma
8.2.1.
Multiple Myeloma
8.2.2.
Solitary Myeloma (Plasmacytoma)
8.2.3.
Osteosclerotic Myeloma
8.3.
Malignant Lymphoma
9.
Notochordal Tumors
9.1.
Chordoma
9.2.
Chondroid Chordoma
9.3.
Dedifferentiated Chordoma
10.
Vascular Tumors
10.1.
Benign Vascular Tumors
10.1.1.
Hemangioma
10.1.2.
Massive Osteolysis
10.1.3.
Glomus Tumor
10.2.
Malignant Vascular Tumors
10.2.1.
Angiosarcoma
10.2.2.
Epithelioid Hemangioendothelioma
10.2.3.
Hemangiopericytoma
11.
Giant Cell Tumor
11.1.
Giant Cell Tumor
11.2.
Malignancy in Giant Cell Tumors
12.
Adamantinoma of Long Bones
12.1.
Adamantinoma
13.
Miscellaneous Tumors
13.1.
Neurilemmoma of Bone
13.2.
Lipoma of Bone
13.3.
Liposarcoma
13.4.
Clear Cell Sarcoma
13.5.
Alveolar Soft Part Sarcoma
13.6.
Leiomyosarcoma
14.
Conditions that Simulate Primary Neoplasms of Bone
14.1.
Metastatic Malignancy
14.2.
Cystic Lesions of Bone that Simulate Neoplasms
14.2.1.
Aneurysmal Bone Cyst
14.2.2.
Simple Cyst
14.2.3.
Intraosseous Ganglion
14.2.4.
Epidermoid Cyst
14.2.5.
Subungual Keratoacanthoma
14.3.
Fibrous Lesions of Bone that Simulate Neoplasms
14.3.1.
Metaphyseal Fibrous Defect
14.3.2.
Periosteal Desmoid (Avulsive Cortical Irregularity)
14.3.3.
Fibrous Dysplasia
14.3.4.
Osteofibrous Dysplasia
14.3.5.
Congenital Fibromatosis (Myofibromatosis)
14.3.6.
Fibrocartilaginous Mesenchymoma
14.4.
Bone-Forming Lesions that Simulate Neoplasms
14.4.1.
Heterotopic Ossification
14.4.2.
Subungual Exostosis
14.4.3.
Bizarre Parosteal Osteochondromatous Proliferation
14.4.4.
Fracture Callus
14.4.5.
Stress (Insufficiency) Fracture
14.4.6.
Bone Island
14.5.
Miscellaneous Conditions that Simulate Neoplasm
14.5.1.
Giant Cell Reparative Granuloma
14.5.2.
Langerhans' Cell Histiocytosis (Eosinophilic Granuloma)
14.6.
Erdheim-Chester Disease
14.6.1.
Mast Cell Disease
14.6.2.
Sinus Histiocytosis with Massive Lymphadenopathy (Rosai-Dorfman Disease)
14.6.3.
Osteomyelitis
14.6.4.
Paget's Disease
14.6.5.
Hyperparathyroidism
14.6.6.
Infarct of Bone
14.6.7.
Transient Osteoporosis
14.6.8.
Traumatic Osteolysis
14.6.9.
Chest Wall Hamartoma
14.6.10.
Neuropathic Joint
14.6.11.
Calcifying Pseudoneoplasm
15.
Synovial Tumors
15.1.
Pigmented Villonodular Synovitis
15.2.
Malignant Pigmented Villanodular Synovitis
15.3.
Synovial Chondromatosis
15.4.
Chondrosarcoma of Synovium
15.5.
Hemangioma
15.6.
Lipoma
The Physical Object
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