rdf-syntax-grammar
mods:
  schema location: http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-2.xsd
  title info:
    title: Atlas of Musculoskeletal Tumors and Tumorlike Lesions
    sub title: The Rizzoli Case Archive
  name:
    name part: Picci, Piero.
    role:
      role term: editor.
  name:
    name part: Manfrini, Marco.
    role:
      role term: editor.
  name:
    name part: Fabbri, Nicola.
    role:
      role term: editor.
  name:
    name part: Gambarotti, Marco.
    role:
      role term: editor.
  name:
    name part: Vanel, Daniel.
    role:
      role term: editor.
  name:
    name part: SpringerLink (Online service)
  type of resource: text
  origin info:
    place:
      place term: gw
    date issued: 2014
    issuance: monographic
  language:
    language term: eng
  physical description:
    form: electronic
    form: electronic resource
    reformatting quality: access
    form: remote
    extent: XXII, 387 p. 226 illus., 173 illus. in color. online resource.
  abstract: This book reflects the experience of the Rizzoli Orthopedic Institute during more than 100 years of treatment of musculoskeletal tumor and tumorlike lesions. It presents a wide range of lesions from a multidisciplinary perspective, highlighting pertinent clinical, radiological, and histological correlations. Treatment is briefly reported for each entity. In addition, the more recent biomolecular findings of use for diagnosis, prognosis, and treatment are carefully analyzed. The Rizzoli case archive spans more than a century, the first treated case dating back to 28 September 1900, and contains the original material – clinical charts, imaging, paraffin blocks, and histological slides – of more than 40,000 cases, including about 29,000 bone lesions and 11,000 soft tissue lesions. This book reports the most relevant entities and reflects the improvements in knowledge of musculoskeletal tumors as presented during the yearly international course held at the Rizzoli Institute. .
  table of contents: Staging. Bone Tumors: Histiocytic Fibroma -- Multiple Histiocytic Fibromas with Extraskeletal Abnormalitie -- Fibrous Dysplasia -- Osteofibrous Dysplasia of Long Bones -- Simple Bone Cyst -- Histiocytosis X.-Chondroma -- Periosteal Chondroma -- Multiple Chondromas -- Osteoid Osteoma.- Osteoblastoma.-Aneurysmal Bone Cyst -- Giant Cell Tumor -- Chondroblastoma.- Chondromyxoid Fibroma -- Chondromyxoid Fibroma -- Desmoid Fibroma -- Chondrosarcomas -- Osteosarcomas.- Malignant Fibrous Histiocytoma -- Fibrosarcoma -- Ewing’s Family Tumors -- Adamantinoma -- Vascular Tumors -- Chordoma -- Primary Lymphoma of Bone -- Multiple Myeloma -- Metastatic Carcinoma Soft Tissue Tumors: Myositis Ossificans -- Pigmented Villo-Nodular Synovitis and Giant Cell Tumor of Tendon Sheath -- Synovial Chondromatosis -- Fibromatosis -- Lipomas -- Liposarcomas -- Dermatofibrosarcoma Protuberans -- Fibrosarcoma -- Leiomyosarcoma -- Rhabdomyosarcoma -- Vascular Tumors -- Solitary Fibrous Tumor -- Neurofibromas.-Schwannoma -- Malignant Schwannoma -- Myofibroblastic Sarcoma -- Undifferentiated Pleomorphic Sarcoma -- Myxofibrosarcoma -- Synovial Sarcoma -- Alveolar Soft Part Sarcoma -- Epithelioid Sarcoma -- Clear Cell Sarcoma -- Extraskeletal Myxoid Chondrosarcoma -- Extraskeletal Osteosarcoma -- Extraskeletal Ewing’s Sarcoma.
  note: edited by Piero Picci, Marco Manfrini, Nicola Fabbri, Marco Gambarotti, Daniel Vanel.
  subject:
    topic: Medicine
  subject:
    topic: Radiology
  subject:
    topic: Oncology
  subject:
    topic: Pathology
  subject:
    topic: Surgery
  subject:
    topic: Medicine & Public Health
  subject:
    topic: Oncology
  subject:
    topic: Surgery
  subject:
    topic: Pathology
  subject:
    topic: Imaging / Radiology
  classification: RC254-282
  classification: 616.994
  related item:
    title info:
      title: Springer eBooks
  identifier: 9783319017488
  identifier: http://dx.doi.org/10.1007/978-3-319-01748-8
  record info:
    record creation date: 140117
    record change date: 20151204175826.0
    record identifier: 978-3-319-01748-8