دانلود کتاب Diagnosis and Management of Primary Bone Tumors: Volume 2

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Contents
Part I: Osteoclastic Giant Cell-Rich Tumors
1: Giant Cell Tumor
1.1 Definition
1.2 Synonym
1.3 Incidence
1.4 Age
1.5 Location
1.6 Clinical Features
1.7 Grading System
1.8 Radiologic Findings
1.9 Histologic Findings
1.10 Management
1.11 Clinical Course and Prognosis
References
2: Brown Tumor of Hyperparathyroidism
2.1 Definition
2.2 Synonym
2.3 Incidence
2.4 Age
2.5 Locations
2.6 Clinical Manifestations
2.7 Radiologic Findings
2.8 Histologic Findings
2.9 Management
2.10 Clinical Course
References
3: Giant Cell Reparative Granuloma
3.1 Definition
3.2 Possible Pathogenesis
3.3 Synonym
3.4 Incidence
3.5 Age
3.6 Location
3.7 Clinical Features
3.8 Radiologic Findings
3.9 Histologic Findings
3.10 Management
3.11 Prognosis
References
Part II: Hematopoietic Tumors
4: Langerhans Cell Histiocytosis
4.1 Definition
4.2 Possible Pathogenesis
4.3 Synonyms
4.4 Incidence
4.5 Age
4.6 Location
4.7 Clinical Features
4.8 Radiologic Findings
4.9 Histologic Findings
4.10 Special Stains
4.11 Management
4.12 Clinical Course
References
5: Plasma Cell Myeloma/Multiple Myeloma
5.1 Definition
5.2 Synonym
5.3 Incidence
5.4 Age
5.5 Location
5.6 Clinical Features and Diagnostic Analysis
5.7 Radiologic Findings
5.8 Histologic Findings
5.9 Special Stains
5.10 Management
5.11 Clinical Course
References
6: Amyloidosis Associated with Plasma Cell Myeloma
6.1 Definition
6.2 Classification
6.3 Clinical Features and Diagnostic Analysis
6.4 Radiologic Findings
6.5 Histologic Findings
6.6 Management
6.7 Clinical Course
References
7: Solitary Plasmacytoma
7.1 Definition
7.2 Age
7.3 Incidence
7.4 Location
7.5 Clinical Features and Diagnostic Analysis
7.6 Radiologic Findings
7.7 Management
7.8 Clinical Course
References
8: Lymphoma of Bone
8.1 Definition
8.2 Synonym
8.3 Incidence
8.4 Age
8.5 Location
8.6 Clinical Features
8.7 Radiologic Findings
8.8 MR Findings
8.9 Histologic Findings
8.10 Special Stains
8.11 Management
8.12 Clinical Course
References
Part III: Notochordal Tumors
9: Benign Notochordal Cell Tumor
9.1 Definition
9.2 Synonyms
9.3 Incidence
9.4 Age
9.5 Location
9.6 Clinical Presentations
9.7 Radiologic Findings
9.8 Histologic Findings
9.9 Management
9.10 Clinical Course
References
10: Chordoma
10.1 Definition
10.2 Incidence
10.3 Age
10.4 Location
10.5 Clinical Presentations
10.6 Radiologic Findings
10.7 Histologic Findings
10.8 Special Stains
10.9 Management and Prognosis
References
Part IV: Cysts and Cyst-Like Lesions
11: Aneurysmal Bone Cyst
11.1 Definition
11.2 Possible Pathogenesis
11.3 Clinical Importance
11.4 Incidence
11.5 Age
11.6 Location
11.7 Clinical Features
11.8 Radiologic Findings
11.9 Histologic Findings
11.10 Management
11.11 Clinical Course
References
12: Simple/Unicameral Bone Cyst
12.1 Definition
12.2 Synonym
12.3 Incidence
12.4 Age
12.5 Location
12.6 Clinical Features
12.7 Radiologic Findings
12.8 Histologic Findings
12.9 Management
12.10 Clinical Course
References
13: Ganglion Cyst
13.1 Definition
13.2 A Possible Mechanism
13.3 Incidence
13.4 Age
13.5 Location
13.6 Clinical Presentation
13.7 Radiologic Findings
13.8 Management
13.9 Prognosis
References
14: Epidermal Inclusion Cyst
14.1 Definition
14.2 Synonyms
14.3 Incidence
14.4 Age
14.5 Location
14.6 Clinical Presentation
14.7 Radiologic Findings
14.8 Management
14.9 Prognosis
References
Part V: Vascular Tumors
15: Hemangioma
15.1 Definition
15.2 Incidence
15.3 Age
15.4 Location
15.5 Clinical Presentation
15.6 Radiologic Findings
15.7 Histologic Findings
15.8 Special Stains
15.9 Management
References
16: Epithelioid Hemangioma
16.1 Definition
16.2 Incidence
16.3 Age
16.4 Location
16.5 Clinical Presentation
16.6 Radiologic Findings
16.7 Histologic Findings
16.8 Special Stains
16.9 Molecular Gene Analysis
16.10 Management
References
17: Glomus Tumor
17.1 Definition
17.2 Incidence
17.3 Age
17.4 Location
17.5 Clinical Presentation
17.6 Radiologic Findings
17.7 Histologic Findings
17.8 Management
17.9 Prognosis
References
18: Epithelioid Hemangioendothelioma
18.1 Definition
18.2 Classification
18.3 Incidence
18.4 Age
18.5 Location
18.6 Clinical Presentation
18.7 Radiologic Findings
18.8 Histologic Findings
18.9 Special Stains
18.10 Molecular Gene Analysis
18.11 Management
18.12 Prognosis
References
19: Angiosarcoma
19.1 Definition
19.2 Incidence
19.3 Age
19.4 Location
19.5 Clinical Presentation
19.6 Radiologic Findings
19.7 Histologic Findings
19.8 Special Stains
19.9 Management
19.10 Prognosis
References
Part VI: Neurogenic Tumors
20: Neurilemmoma
20.1 Definition
20.2 Synonym
20.3 Incidence
20.4 Age
20.5 Location
20.6 Clinical Presentation
20.7 Radiologic Findings
20.8 Histologic Findings
20.9 Management
20.10 Prognosis
References
21: Neurofibroma
21.1 Definition
21.2 Incidence
21.3 Age
21.4 Location
21.5 Clinical Presentation
21.6 Radiologic Findings
21.7 Histologic Findings
21.8 Management
21.9 Prognosis
References
22: Neurofibromatosis Affecting Bone
22.1 Definition
22.2 Synonym
22.3 Incidence
22.4 Age
22.5 Skeletal Distribution
22.6 Clinical Presentations
22.7 Radiologic Findings
22.8 Histologic Findings
22.9 Management
22.10 Clinical Course
References
23: Malignant Peripheral Nerve Sheath Tumor
23.1 Definition
23.2 Synonyms
23.3 Incidence
23.4 Age
23.5 Location
23.6 Clinical Presentations
23.7 Radiologic Findings
23.8 Histologic Findings
23.9 Special Stains
23.10 Management
23.11 Prognosis
References
Part VII: Other Mesenchymal Cell Tumors
24: Lipoma
24.1 Definition
24.2 Incidence
24.3 Age
24.4 Location
24.5 Clinical Presentations
24.6 Radiologic Findings
24.7 Histologic Findings
24.8 Management
24.9 Clinical Course
References
25: Ewing’s Sarcoma
25.1 Definition
25.2 Pathogenesis
25.3 Incidence
25.4 Age
25.5 Location
25.6 Clinical Presentations
25.7 Radiologic Findings
25.8 Histologic Findings
25.9 Special Stains
25.10 Management
25.11 Clinical Course and Prognosis
References
26: Undifferentiated Pleomorphic Sarcoma
26.1 Definition
26.2 Incidence
26.3 Age
26.4 Location
26.5 Clinical Features
26.6 Radiologic Findings
26.7 Histologic Findings
26.8 Special Stains
26.9 Management
26.10 Clinical Course and Prognosis
References
27: Leimyosarcoma
27.1 Definition
27.2 Incidence
27.3 Age
27.4 Location
27.5 Clinical Features
27.6 Radiologic Findings
27.7 Histologic Findings
27.8 Special Stains
27.9 Management
27.10 Clinical Course
References
28: Adamantinoma
28.1 Definition
28.2 Possible Histogenesis
28.3 Incidence
28.4 Age
28.5 Location
28.6 Clinical Features
28.7 Radiologic Findings
28.8 Histologic Findings
28.9 Management
28.10 Clinical Course
References