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Management of Soft Tissue Sarcoma addresses the diagnosis and best current management of adult soft tissue sarcomas. Edited by world renonwed experts, this book dileneates and discusses each different sarcoma subtype individually --
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Subjects
Soft tissue tumors, Treatment, Sarcoma, Connective tissues, Tumors, surgeryShowing 4 featured editions. View all 4 editions?
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1
Management of Soft Tissue Sarcoma
2016, Springer International Publishing AG
in English
3319419048 9783319419046
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2
Management of Soft Tissue Sarcoma
2016, Springer London, Limited
in English
3319419064 9783319419060
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3 |
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4
Management of Soft Tissue Sarcoma
2012, Springer London, Limited
in English
1461450047 9781461450047
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Book Details
Table of Contents
Machine generated contents note: 1.General Description
Introduction
Incidence and Prevalence
Predisposing and Genetic Factors
References
2.Natural History: Importance of Size, Site, and Histopathology
Natural History
Influence of Site
Staging
Staging of Retroperitoneal Visceral Sarcoma
Prognostic Factors for Extremity and Superficial Soft Tissue Sarcoma
Disease-Specific Survival
Prognostic Factors for Survival Following Local Recurrence of Extremity Sarcoma
Prognostic Factors: Nomograms
References
3.General Statement as to Efficacy of Surgery/Chemotherapy/Radiation Therapy
Extent of Primary Surgery
Surgical Treatment of Local Recurrence
Diagnostic Imaging
Surgery for Metastatic Disease
Pulmonary Metastasis
Radiation Therapy
Adjuvant Radiation Therapy
Dose of Radiation Therapy
Adjuvant Brachytherapy
Radiation Therapy in the Presence of Positive Microscopic Margins
Definitive Radiation Therapy
Contents note continued: Radiation to Patients with Neurovascular Involvement
Wound Complications of Radiation Therapy
Sarcomas More Common in Adults
Larger Randomized Studies
Selected Meta-analyses of Randomized Trials of Adjuvant Chemotherapy
Adjuvant Therapy for GIST
Sarcomas More Common in the Pediatric Setting
Special Techniques for Primary and Locally Recurrent Disease
Intra-arterial Chemotherapy
Limb Perfusion and Hyperthermia
References
pt. I Management by Histopathology: Introduction
4.Gastrointestinal Stromal Tumors (GISTs)
Imaging
Familial GIST
Natural History
Diagnosis, Molecular Pathology
Treatment
Adjuvant Imatinib for Primary GIST
Neoadjuvant Therapy for Primary Disease Not Amenable to Surgery
Treatment of Recurrence
Systemic Targeted Therapy for Metastatic GIST
Dose Intensity over Time
Imatinib Pharmacokinetics
Second-Line Sunitinib for Imatinib-Resistant Metastatic GIST
Contents note continued: Other Tyrosine Kinase Inhibitors for Metastatic GIST Failing Imatinib and Sunitinib
Newer Agents
References
5.Liposarcoma
Imaging
Diagnosis
Treatment
Radiation Therapy
Systemic Therapy: General Considerations
Adjuvant Therapy
Treatment of Metastatic Disease
Outcomes
Outcome Following Metastasis
References
6.Leiomyosarcoma
Imaging
Diagnosis, Molecular Pathology
Treatment
Radiation Therapy
Systemic Therapy
Adjuvant Chemotherapy
Treatment of Recurrence
Metastatic Disease
Outcome
References
7.Undifferentiated Pleomorphic Sarcoma (UPS; Malignant Fibrous Histiocytoma: MFH) and Myxofibrosarcoma
Imaging
Diagnosis/Molecular Pathology
Natural History
Treatment
Radiation Therapy
Metastatic Disease
Adjuvant Chemotherapy
Outcome
References
8.Synovial Sarcoma
Imaging
Diagnosis, Molecular Pathology
Treatment
Radiation Therapy
Chemotherapy
Contents note continued: Treatment of Recurrence
Local Recurrence
Systemic Treatment
Outcome
References
9.Malignant Peripheral Nerve Sheath Tumor (MPNST) and Triton Tumor
Presentation
Imaging
Diagnosis/Pathology
Neurofibromatosis Type 1 and Outcome
Treatment
Radiation Therapy
Chemotherapy
Outcome
References
10.Desmoid Tumor/Deep-Seated Fibromatosis (Desmoid-Type Fibromatosis)
Clinical Presentation
Imaging
Diagnosis: Molecular
Natural History
Treatment
Treatment of Recurrence
Systemic Therapy
Treatment by Observation
Radiation Therapy
Patterns of Failure
Outcome
References
11.Solitary Fibrous Tumor/Hemangiopericytoma
Outcome
References
12.Fibrosarcoma and Its Variants
Outcome
Dermatofibrosarcoma Protuberans
Outcome
Low-Grade Fibromyxoid Sarcoma (Evans' Tumor)
Outcome
Sclerosing Epithelioid Fibrosarcoma
Inflammatory Myofibroblastic Tumor
Infantile Fibrosarcoma
Contents note continued: Myxoinflammatory Fibroblastic Sarcoma/Inflammatory Myxohyaline Tumor of Distal Extremities
Adult-Type Fibrosarcoma
References
13.Vascular Sarcomas
Epithelioid Hemangioendothelioma
Angiosarcoma/Lymphangiosarcoma
Outcome
Kaposi Sarcoma
References
14.Epithelioid Sarcoma
Outcome
References
15.Sarcomas More Common in Children
Soft Tissue Sarcomas More Commonly Observed in Pediatric Patients
Ewing Sarcoma Family of Tumors (EFT)
Demographics
Primary Therapy
Adjuvant Chemotherapy
High-Dose Systemic Therapy for Metastatic Disease
Standard Cytotoxic Chemotherapy After Disease Relapse
Investigational Approaches
Ewing Sarcoma-Like Small Round Cell Tumors
Rhabdomyosarcoma
Demographics
Molecular Biology
Risk Stratification
Staging
Imaging
Primary Therapy
Chemotherapy for Metastatic Disease
Embryonal Sarcoma
Calcifying Nested Stromal and Epithelial Tumor
References
Contents note continued: 16.Radiation-Induced Sarcomas
References
17.Alveolar Soft Part Sarcoma
Imaging
Diagnosis/Molecular Pathology
Primary Treatment
Treatment of Metastatic Disease
Outcome
References
18.Clear Cell Sarcoma/Melanoma of Soft Parts
Imaging
Diagnosis: Molecular Pathology
Treatment
Outcome
References
19.Desmoplastic Small Round Cell Tumor
Imaging
Diagnosis
Treatment
Outcome
References
20.Extraskeletal Myxoid Chondrosarcoma
Imaging
Diagnosis
Treatment
Outcome
References
21.Other Uterine Sarcomas
Endometrial Stromal Sarcoma
Diagnosis
Treatment
Outcome
Undifferentiated Endometrial Sarcoma
Outcome
Uterine Carcinosarcomas and Other Malignant Mixed Mullerian Tumors
PEComas
Outcome
References
22.Extraskeletal Osteogenic Sarcoma
Imaging
Diagnosis
Treatment
Outcome
References
23.Sustentacular Tumors of Lymph Tissue
Contents note continued: Follicular Dendritic Cell Tumor (Dendritic Reticulum Cell Tumor [FDCT]) and Interdigitating Reticulum Cell Tumor (IDRCT)
True Histiocytic Sarcoma
Langerhans Cell Tumors
Outcome
References
24.Uncommon/Unique Sites
Heart and Great Vessels
Primary Sarcomas of the Breast
Phyllodes Tumor
Diagnosis
Outcome
Head and Neck
Treatment
Primary Sarcomas of the Mediastinum
Liver
References
pt. II Benign and Less Aggressive Lesions: Introduction
25.Mostly Benign/Rarely Metastasizing Soft Tissue Tumor
Ossifying Fibromyxoid Tumor
Perivascular Epithelioid Cell Tumor (PEComa) and Related Entities: Lymphangioleiomyomatosis, Angiomyolipoma, and Sugar Cell Tumor
Therapy
Giant Cell Tumor of Tendon Sheath/Pigmented Villonodular Synovitis
Myoepithelioma of Soft Tissue
Glomus Tumor
References
26.Benign Soft Tissue Tumors
Lipoma
Lipomatosis
Lipoblastoma/Lipoblastomatosis
Angiolipoma
Contents note continued: Angiomyolipoma
Angiomyelolipoma
Hibernoma
Elastofibroma
Granular Cell Tumor
Hemangioma
Leiomyoma
Schwannoma
Neurofibroma
Myxoma
Angiomyxoma
References
27.Reactive Lesions
Myositis Ossificans
Nodular Fasciitis
Sarcoma Masquerade
References.
Edition Notes
Includes bibliographical references and index.
Classifications
The Physical Object
ID Numbers
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Feedback?History
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September 23, 2024 | Edited by MARC Bot | import existing book |
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November 13, 2020 | Created by MARC Bot | Imported from Library of Congress MARC record |