Diagnosis and management of primary bone tumors. Volume 2 / Won-Jong Bahk.
Bahk, Won-Jong, author.
2023
RC280.B6
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Title Diagnosis and management of primary bone tumors. Volume 2 / Won-Jong Bahk.
Author Bahk, Won-Jong, author.
ISBN 9789819954988 (electronic bk.)
9819954983 (electronic bk.)
9819954975
9789819954971
DOI https://doi.org/10.1007/978-981-99-5498-8
Published Singapore : Springer, [2023]
Copyright ©2023
Language English
Description 1 online resource (xiii, 392 pages) : illustrations (chiefly color)
Item Number 10.1007/978-981-99-5498-8 doi
Call Number RC280.B6
Dewey Decimal Classification 616.99/471
Summary This book is the second in a two-volume set that offers comprehensive guidance on the diagnosis of bone tumors based on a modification of the WHO classification as well as management and follow-up. The emphasis throughout is on an integrated approach to diagnosis that highlights the role of clinical, radiologic, and pathologic correlation in reducing the possibility of diagnostic error. The diagnosis of bone tumors is difficult for a variety of reasons, including the numerous types of the tumors with variable subtypes, the protean radiologic manifestations and the variable pathologic findings case by case and even depending on the phase in each case, the presence of reactive changes to the tumor lesion, and overlapping findings between benign and malignant tumors. In addition, it is often more difficult by surgeons inadequate biopsy. The authors aim is to offer the readers the best possible guidance in negotiating these difficulties. For each tumor types, a wide range of cases are presented, from the common to the very rare. Appearances on the full range of imaging studies are illustrated, including conventional radiographs, bone scans, CT scan, MRI, and even PET/CT scans in malignant cases. Attention is also drawn to the role of long-term follow-up radiographs in ensuring correct diagnosis and management. This book will be an ideal resource for all practitioners and researchers who involved in bone tumor diagnosis and also management. Volume 2 covers osteoclastic giant cell-rich tumors, hematopoietic tumors, notochordal tumors, cysts and cyst-like lesions, vascular and neurogenic tumors, and tumors of other mesenchymal cells.
Bibliography, etc. Note Includes bibliographical references.
Access Note Access limited to authorized users.
Source of Description Online resource; title from PDF title page (SpringerLink, viewed December 13, 2023).
Available in Other Form Print version: 9789819954971
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Intro
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

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