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Soft tissue pathology for clinicians
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  • Soft tissue pathology for clinicians
Utgivning, distribution etc.
  • Springer, Cham : 2017.
National Library of Medicine (NLM) klassifikationskod
  • WD 375
DDC klassifikationskod (Dewey Decimal Classification)
Fysisk beskrivning
  • 1 online resource.
Serietitel - ej biuppslagsform
Anmärkning: Bibliografi etc.
  • Includes bibliographical references and index.
Anmärkning: Innehåll
  • 1. Critical concepts in soft tissue pathology -- 2. Histologic examination and ancillary studies in soft tissue pathology -- 3. Grading, staging, and reporting of soft tissue tumors -- 4. Lipomatous tumors -- 5. Fibroblastic/Myofibroblastic tumors -- 6. Fibrohistiocytic lesions -- 7. Smooth muscle and perivascular tumors -- 8. Skeletal muscle tumors -- 9. Neural and nerve shealth lesions -- 10. Vascular lesions -- 11. Cartilaginous and osseous tumors of soft tissue -- 12. Tumors of uncertain differentiation -- 13. Gastrointestinal stromal tumor.
  • Dedication; Preface; Contents; 1: Critical Concepts in Soft Tissue Pathology; 1.1 General Principles of Classification; 1.2 Acquisition, Handling, and Processing of Soft Tissue Specimens; References; 2: Histologic Examination and Ancillary Studies in Soft Tissue Pathology; 2.1 Pathologist Approach to Diagnosis; 2.2 Diagnostic Ancillary Studies; 2.2.1 Immunohistochemistry; 2.2.2 Karyotyping; 2.2.3 Molecular Fluorescence In Situ Hybridization; 2.2.4 Reverse transcription PCR; 2.3 Intraoperative Consultation; References; 3: Grading, Staging, and Reporting of Soft Tissue Tumors.
  • 3.1 Assigning a Pathologic Grade to Soft Tissue Tumors3.2 Assigning a Pathologic Stage to Soft Tissue Tumors; 3.3 Interpreting a Soft Tissue Pathology Report; References; 4: Lipomatous Tumors; 4.1 Lipoma; 4.2 Angiolipoma; 4.3 Spindle Cell/Pleomorphic Lipoma; 4.4 Hibernoma; 4.5 Lipoblastoma; 4.6 Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma; 4.7 Dedifferentiated Liposarcoma; 4.8 Myxoid Liposarcoma; 4.9 Pleomorphic Liposarcoma; References; 5: Fibroblastic/Myofibroblastic Tumors; 5.1 Nodular Fasciitis and Similar Lesions; 5.2 Fibroma of Tendon Sheath.
  • 5.3 Nuchal-Type Fibroma5.4 Gardner-Associated Fibroma; 5.5 Elastofibroma; 5.6 Superficial Fibromatosis; 5.7 Deep (Desmoid-Type) Fibromatosis; 5.8 Solitary Fibrous Tumor; 5.9 Inflammatory Myofibroblastic Tumor; 5.10 Dermatofibrosarcoma Protuberans; 5.11 Congenital/Infantile Fibrosarcoma; 5.12 Low-Grade Fibromyxoid Sarcoma; 5.13 Myxofibrosarcoma; 5.14 Adult-Type Fibrosarcoma; References; 6: Fibrohistiocytic Lesions; 6.1 Fibrous Histiocytoma; 6.2 Solitary Xanthogranuloma; 6.3 Tenosynovial Giant Cell Tumor, Localized Type; 6.4 Tenosynovial Giant Cell Tumor, Diffuse Type.
  • 10.2 Epithelioid Hemangioendothelioma10.3 Kaposiform Hemangioendothelioma; 10.4 Angiosarcoma; References; 11: Cartilaginous and Osseous Tumors of Soft Tissue; 11.1 Extraskeletal Chondroma; 11.2 Extraskeletal Mesenchymal Chondrosarcoma; 11.3 Extraskeletal Osteosarcoma; References; 12: Tumors of Uncertain Differentiation; 12.1 Intramuscular Myxoma; 12.2 Superficial Angiomyxoma; 12.3 Hemosiderotic Fibrolipomatous Tumor; 12.4 Myoepithelioma of Soft Tissue; 12.5 Ossifying Fibromyxoid Tumor; 12.6 Alveolar Soft Part Sarcoma; 12.7 Clear Cell Sarcoma of Soft Tissue.
Anmärkning: Innehållsbeskrivning, sammanfattning
  • This text is constructed to educate clinicians on the general classification and diagnostic approach to soft tissue tumors, such that they feel more empowered to discuss the relevant features of particular cases with their pathology colleagues. Particular consideration is given to diagnostically and prognostically relevant ancillary studies. The first section addresses the basic foundations of soft tissue pathology, including common morphologic patterns, approach to grading, concepts of immunohistochemistry and molecular studies. Following this introductory section, each soft tissue tumor is presented according to its morphologic differentiation. Sections include lipomatous tumors, fibrous lesions, fibrohistiocytic tumors, neural and nerve sheath tumors, and smooth muscle neoplasms. Each entity is presented in a consistent and organized manner, first discussing the clinical presentation and then addressing the gross and microscopic features. Following this, the immunohistochemical and molecular findings are presented The text then briefly discusses prognosis and treatment. Representative photographs of the microscopic appearance will be included in a large format. Soft Tissue Pathology for Clinicians will further patient care by concisely educating the clinician on the relevant aspects of soft tissue diagnostics.
Term
Genre/Form
  • Electronic books.
Annat medium
  • Print version: Perry, Kyle. Soft tissue pathology for clinicians. Cham : Springer, 2017 ISBN 9783319556536 ISBN 3319556533
Seriebiuppslag under titel
  • Pathology for clinicians.
Elektronisk adress och åtkomst (URI)
  • http://link.springer.com/10.1007/978-3-319-55654-3
ISBN
  • 9783319556543
  • 3319556541
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*5050 $aDedication; Preface; Contents; 1: Critical Concepts in Soft Tissue Pathology; 1.1 General Principles of Classification; 1.2 Acquisition, Handling, and Processing of Soft Tissue Specimens; References; 2: Histologic Examination and Ancillary Studies in Soft Tissue Pathology; 2.1 Pathologist Approach to Diagnosis; 2.2 Diagnostic Ancillary Studies; 2.2.1 Immunohistochemistry; 2.2.2 Karyotyping; 2.2.3 Molecular Fluorescence In Situ Hybridization; 2.2.4 Reverse transcription PCR; 2.3 Intraoperative Consultation; References; 3: Grading, Staging, and Reporting of Soft Tissue Tumors.
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*5058 $a5.3 Nuchal-Type Fibroma5.4 Gardner-Associated Fibroma; 5.5 Elastofibroma; 5.6 Superficial Fibromatosis; 5.7 Deep (Desmoid-Type) Fibromatosis; 5.8 Solitary Fibrous Tumor; 5.9 Inflammatory Myofibroblastic Tumor; 5.10 Dermatofibrosarcoma Protuberans; 5.11 Congenital/Infantile Fibrosarcoma; 5.12 Low-Grade Fibromyxoid Sarcoma; 5.13 Myxofibrosarcoma; 5.14 Adult-Type Fibrosarcoma; References; 6: Fibrohistiocytic Lesions; 6.1 Fibrous Histiocytoma; 6.2 Solitary Xanthogranuloma; 6.3 Tenosynovial Giant Cell Tumor, Localized Type; 6.4 Tenosynovial Giant Cell Tumor, Diffuse Type.
*5058 $a10.2 Epithelioid Hemangioendothelioma10.3 Kaposiform Hemangioendothelioma; 10.4 Angiosarcoma; References; 11: Cartilaginous and Osseous Tumors of Soft Tissue; 11.1 Extraskeletal Chondroma; 11.2 Extraskeletal Mesenchymal Chondrosarcoma; 11.3 Extraskeletal Osteosarcoma; References; 12: Tumors of Uncertain Differentiation; 12.1 Intramuscular Myxoma; 12.2 Superficial Angiomyxoma; 12.3 Hemosiderotic Fibrolipomatous Tumor; 12.4 Myoepithelioma of Soft Tissue; 12.5 Ossifying Fibromyxoid Tumor; 12.6 Alveolar Soft Part Sarcoma; 12.7 Clear Cell Sarcoma of Soft Tissue.
*520  $aThis text is constructed to educate clinicians on the general classification and diagnostic approach to soft tissue tumors, such that they feel more empowered to discuss the relevant features of particular cases with their pathology colleagues. Particular consideration is given to diagnostically and prognostically relevant ancillary studies. The first section addresses the basic foundations of soft tissue pathology, including common morphologic patterns, approach to grading, concepts of immunohistochemistry and molecular studies. Following this introductory section, each soft tissue tumor is presented according to its morphologic differentiation. Sections include lipomatous tumors, fibrous lesions, fibrohistiocytic tumors, neural and nerve sheath tumors, and smooth muscle neoplasms. Each entity is presented in a consistent and organized manner, first discussing the clinical presentation and then addressing the gross and microscopic features. Following this, the immunohistochemical and molecular findings are presented The text then briefly discusses prognosis and treatment. Representative photographs of the microscopic appearance will be included in a large format. Soft Tissue Pathology for Clinicians will further patient care by concisely educating the clinician on the relevant aspects of soft tissue diagnostics.
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