Campanacci Bone and Soft Tissue Tumors

Clinical Features, Imaging, Pathology and Treatment
2. Auflage 1999
ISBN: 978-3-7091-3846-5
Verlag: Springer Wien
Format: PDF
Kopierschutz: 1 - PDF Watermark

E-Book, Englisch, 1320 Seiten, eBook

to the first edition (1990) This is an extraordinary book by an extraordinary author. Mario Campanacci first pub lished three volumes on musculoskeletal neoplasms and other tumor-like processes in bone and soft parts in Italian in 1981-1985. This book is an update and expansion of that book, published for the first time in English. In this book Dr. Campanacci brings to the readers the vast experience in musculoskeletal oncology of the Rizzoli Orthopaedic Institute in Bologna where he has been head of the Oncology Unit for many years. As such, he has had at his dis posal the patient records, radiographs and pathologic material dating back to 1905. In fact, a visitor to the Institute will be shown the radiograph made of the first tumor case on record- that of a giant cell tumor of the distal femur. The wealth of clinical material that has been ac cumulated at the Rizzoli Institute, with exquisite documentation and maintenance is a unique resource and testimonial to not only the author but his predecessors. Under Campanacci' s leadership, the Institute has provided care to the majority of patients with neoplasms through out Italy. Over the past two decades a treatment team with extraordinary ability in radiology, imaging, pathology, chemotherapy, as well as orthopedic surgery has been assembled.

Zielgruppe

Professional/practitioner

Autoren/Hrsg.

Campanacci, Mario

Weitere Mitwirkende

Enneking, W.F.

Inhaltsverzeichnis

1. Introduction.- Bone Tumors.- 2. Histiocytic fibroma.- 3. Benign fibrous histiocytoma.- 4. Giant cell tumor.- 5. Desmoid fibroma.- 6. Fibrosarcoma.- 7. Malignant fibrous histiocytoma.- 8. Leiomyosarcoma.- 9. Exostosis.- 10. Multiple hereditary exostoses.- 11. Hemimelic epiphyseal dysplasia.- 12. Chondroma.- 13. Periosteal chondroma.- 14. Multiple chondromas.- 15. Chondroblastoma.- 16. Chondromyxoid fibroma.- 17. Fibrocartilaginous mesenchymoma.- 18. Central chondrosarcoma.- 19. Dedifferentiated central chondrosarcoma.- 20. Peripheral chondrosarcoma.- 21. Periosteal chondrosarcoma.- 22. Clear cell chondrosarcoma.- 23. Mesenchymal chondrosarcoma.- 24. Osteoma and bone islands.- 25. Osteoid osteoma.- 26. Osteoblastoma.- 27. Fibrous dysplasia.- 28. High grade osteosarcomas.- 29. Periosteal osteosarcoma.- 30. Parosteal osteosarcoma.- 31. Central low-grade osteosarcoma.- 32. Primary lymphoma of bone.- 33. Hodgkin’s disease.- 34. Leukemia.- 35. Multiple myeloma.- 36. Hemangioma.- 37. Limphangioma, cystic angiomatosis.- 38. Hemangioendothelioma, benign, low-grade, high-grade (angiosarcoma).- 39. Hemangiopericytoma.- 40. Neurilemoma, neurofibroma.- 41. Ewing’s sarcoma, primitive neurectodermal tumor (PNET).- 42. Lipoma, liposarcoma, malignant mesenchymoma.- 43. Chordoma.- 44. Osteofibrous dysplasia and adamantinoma.- 45. Sarcoma in Paget’s disease.- 46. Carcinoma and sarcoma in chronic osteomyelitis.- 47. The effects of radiation on the skeleton and radiation induced sarcomas (of bone and soft tissues).- 48. Sarcomas on bone infarct, bone necrosis, or at the site of metallic implants.- 49. Metastatic bone disease.- Tumorlike Lesions of Bone.- 50. Simple bone cyst.- 51. Aneurysmal bone cyst.- 52. Intraosseous and periosteal mucous cyst.- 53. Massive idiopathicosteolysis.- 54. Langherans’ cell histiocytosis.- 55. “Brown tumors” in primary hyperparathyroidism.- 56. Reparative giant cell granuloma.- Soft Tissue Tumors.- 57. (Subdermal) fibrous hamartoma of infancy.- 58. Infantile digital fibromatosis.- 59. Calcifying aponeurotic fibroma.- 60. Infantile myofibroma, myofibromatosis.- 61. Aggressive fibromatosis.- 62. Fibrosarcoma.- 63. Benign fibrous histiocytoma.- 64. Dermatofibrosarcoma protuberans.- 65. Atypical fibroxanthoma of the skin.- 66. Subcutaneous angiomatoid fibrous histiocytoma.- 67. Malignant fibrous histiocytoma.- 68. Lipomas.- 69. Liposarcoma.- 70. Leiomyoma.- 71. Leiomyosarcoma.- 72. Rhabdomyoma.- 73. Rhabdomyosarcoma.- 74. Angiomas and angiodysplasias.- 75. Glomus tumor.- 76. Epithelioid hemangioendothelioma and angiosarcoma.- 77. Kaposi’s sarcoma.- 78. Hemangiopericytoma.- 79. Synovial sarcoma.- 80. Neurilemoma.- 81. Neurofibroma, neurofibromatosis.- 82. Granular cell tumor.- 83. Malignant peripheral nerve sheath tumor.- 84. Clear cell sarcoma of tendons and aponeuroses.- 85. Ganglioneuroma, Ganglioneuroblastoma, neuroblastoma.- 86. Primitive neurectodermal tumor (PNET) and extraskeletal Ewing’s sarcoma.- 87. Extraskeletal chondrosarcomas.- 88. Extraskeletal osteosarcoma.- 89. Alveolar soft part sarcoma.- 90. Epithelioid sarcoma.- Tumorlike Lesions of the Soft Tissues.- 91. Palmar fibromatosis (Dupuytren’s d.), plantar fibromatosis (Ledderhose’s d.).- 92. Nodular fasciitis, proliferative fasciitis, proliferative myositis.- 93. Elastofibroma.- 94. Xanthoma.- 95. Intramuscular myxoma.- 96. Mucous cyst.- 97. Amputation neuroma.- 98. Synovial chondromatosis, extraskeletal chondroma, synovial chondrosarcoma.- 99. Tumoral calcinosis.- 100. Pseudotumoral soft tissue and periosteal ossifications.- 101.Pigmented villo-nodular synovitis.