001484437 000__ 06481cam\\2200589\i\4500 001484437 001__ 1484437 001484437 003__ OCoLC 001484437 005__ 20240117003324.0 001484437 006__ m\\\\\o\\d\\\\\\\\ 001484437 007__ cr\cn\nnnunnun 001484437 008__ 231202s2023\\\\si\a\\\\ob\\\\000\0\eng\d 001484437 019__ $$a1411306904 001484437 020__ $$a9789819954988$$q(electronic bk.) 001484437 020__ $$a9819954983$$q(electronic bk.) 001484437 020__ $$z9819954975 001484437 020__ $$z9789819954971 001484437 0247_ $$a10.1007/978-981-99-5498-8$$2doi 001484437 035__ $$aSP(OCoLC)1411185022 001484437 040__ $$aYDX$$beng$$erda$$epn$$cYDX$$dOCLCO$$dGW5XE$$dEBLCP$$dOCLCO 001484437 049__ $$aISEA 001484437 050_4 $$aRC280.B6 001484437 08204 $$a616.99/471$$223/eng/20231213 001484437 1001_ $$aBahk, Won-Jong,$$eauthor. 001484437 24510 $$aDiagnosis and management of primary bone tumors.$$nVolume 2 /$$cWon-Jong Bahk. 001484437 264_1 $$aSingapore :$$bSpringer,$$c[2023] 001484437 264_4 $$c©2023 001484437 300__ $$a1 online resource (xiii, 392 pages) :$$billustrations (chiefly color) 001484437 336__ $$atext$$btxt$$2rdacontent 001484437 337__ $$acomputer$$bc$$2rdamedia 001484437 338__ $$aonline resource$$bcr$$2rdacarrier 001484437 504__ $$aIncludes bibliographical references. 001484437 5050_ $$aIntro -- Contents -- Part I: Osteoclastic Giant Cell-Rich Tumors -- 1: Giant Cell Tumor -- 1.1 Definition -- 1.2 Synonym -- 1.3 Incidence -- 1.4 Age -- 1.5 Location -- 1.6 Clinical Features -- 1.7 Grading System -- 1.8 Radiologic Findings -- 1.9 Histologic Findings -- 1.10 Management -- 1.11 Clinical Course and Prognosis -- References -- 2: Brown Tumor of Hyperparathyroidism -- 2.1 Definition -- 2.2 Synonym -- 2.3 Incidence -- 2.4 Age -- 2.5 Locations -- 2.6 Clinical Manifestations -- 2.7 Radiologic Findings -- 2.8 Histologic Findings -- 2.9 Management 001484437 5058_ $$a2.10 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 001484437 5058_ $$a4.10 Special Stains -- 4.11 Management -- 4.12 Clinical Course -- References -- 5: Plasma Cell Myeloma/Multiple Myeloma -- 5.1 Definition -- 5.2 Synonym -- 5.3 Incidence -- 5.4 Age -- 5.5 Location -- 5.6 Clinical Features and Diagnostic Analysis -- 5.7 Radiologic Findings -- 5.8 Histologic Findings -- 5.9 Special Stains -- 5.10 Management -- 5.11 Clinical Course -- References -- 6: Amyloidosis Associated with Plasma Cell Myeloma -- 6.1 Definition -- 6.2 Classification -- 6.3 Clinical Features and Diagnostic Analysis -- 6.4 Radiologic Findings -- 6.5 Histologic Findings 001484437 5058_ $$a6.6 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 001484437 5058_ $$aPart III: Notochordal Tumors -- 9: Benign Notochordal Cell Tumor -- 9.1 Definition -- 9.2 Synonyms -- 9.3 Incidence -- 9.4 Age -- 9.5 Location -- 9.6 Clinical Presentations -- 9.7 Radiologic Findings -- 9.8 Histologic Findings -- 9.9 Management -- 9.10 Clinical Course -- References -- 10: Chordoma -- 10.1 Definition -- 10.2 Incidence -- 10.3 Age -- 10.4 Location -- 10.5 Clinical Presentations -- 10.6 Radiologic Findings -- 10.7 Histologic Findings -- 10.8 Special Stains -- 10.9 Management and Prognosis -- References -- Part IV: Cysts and Cyst-Like Lesions 001484437 506__ $$aAccess limited to authorized users. 001484437 520__ $$aThis book is the second in a two-volume set that offers comprehensive guidance on the diagnosis of bone tumors based on a modification of the WHO classification as well as management and follow-up. The emphasis throughout is on an integrated approach to diagnosis that highlights the role of clinical, radiologic, and pathologic correlation in reducing the possibility of diagnostic error. The diagnosis of bone tumors is difficult for a variety of reasons, including the numerous types of the tumors with variable subtypes, the protean radiologic manifestations and the variable pathologic findings case by case and even depending on the phase in each case, the presence of reactive changes to the tumor lesion, and overlapping findings between benign and malignant tumors. In addition, it is often more difficult by surgeons inadequate biopsy. The authors aim is to offer the readers the best possible guidance in negotiating these difficulties. For each tumor types, a wide range of cases are presented, from the common to the very rare. Appearances on the full range of imaging studies are illustrated, including conventional radiographs, bone scans, CT scan, MRI, and even PET/CT scans in malignant cases. Attention is also drawn to the role of long-term follow-up radiographs in ensuring correct diagnosis and management. This book will be an ideal resource for all practitioners and researchers who involved in bone tumor diagnosis and also management. Volume 2 covers osteoclastic giant cell-rich tumors, hematopoietic tumors, notochordal tumors, cysts and cyst-like lesions, vascular and neurogenic tumors, and tumors of other mesenchymal cells. 001484437 588__ $$aOnline resource; title from PDF title page (SpringerLink, viewed December 13, 2023). 001484437 650_0 $$aBones$$xTumors$$xDiagnosis. 001484437 650_0 $$aBones$$xTumors$$xTreatment. 001484437 650_6 $$aOs$$xTumeurs$$xTraitement. 001484437 655_0 $$aElectronic books. 001484437 77608 $$iPrint version: $$z9819954975$$z9789819954971$$w(OCoLC)1389606264 001484437 852__ $$bebk 001484437 85640 $$3Springer Nature$$uhttps://univsouthin.idm.oclc.org/login?url=https://link.springer.com/10.1007/978-981-99-5498-8$$zOnline Access$$91397441.1 001484437 909CO $$ooai:library.usi.edu:1484437$$pGLOBAL_SET 001484437 980__ $$aBIB 001484437 980__ $$aEBOOK 001484437 982__ $$aEbook 001484437 983__ $$aOnline 001484437 994__ $$a92$$bISE