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DIAGNOSTIC PATHOLOGY: SOFT TISSUE TUMORS

9780323661102 ::  DIAGNOSTIC PATHOLOGY: SOFT TISSUE TUMORS
ISBN:

9780323661102

EditorialELSEVIER SCIENCE PUB.B.U.
Edicion:
Páginas:920
Idioma:INGLES
P.V.P.: 259,99 € + 4% IVA = 270,39 €
Dto 5% Ahorras 13,52 €
Importe final iva incl. 256,87 €
PLAZO DE ENTREGA 15 DIAS
Otras versiones :

<P>COVERING ALL ASPECTS OF SOFT TISSUE PATHOLOGY, THIS HIGHLY REGARDED VOLUME IN THE <I>DIAGNOSTIC PATHOLOGY</I> SERIES IS AN<B> EXCELLENT POINT-OF-CARE RESOURCE FOR PATHOLOGISTS AT ALL LEVELS OF EXPERIENCE AND TRAINING</B>-BOTH AS A QUICK REFERENCE AND AS AN EFFICIENT REVIEW TO IMPROVE KNOWLEDGE AND SKILLS. SPECIFICALLY DESIGNED AS A POINT-OF-CARE RESOURCE, THE UPDATED THIRD EDITION USES A TEMPLATED, HIGHLY FORMATTED DESIGN; CONCISE, BULLETED TEXT; AND SUPERIOR COLOR IMAGES THROUGHOUT THAT DEMONSTRATE THE VARIETY OF DIFFERENTIATING FACTORS IN SOFT TISSUE TUMORS.</P>

<P>SOFT TISSUE INTRODUCTION</P> <P>INTRODUCTION AND OVERVIEW</P> <P>GROSS EXAMINATION</P> <P>GRADING AND STAGING</P> <P>ANCILLARY TECHNIQUES</P> <P>SOFT TISSUE IMMUNOHISTOCHEMISTRY</P> <P>MOLECULAR FEATURES OF SOFT TISSUE TUMORS</P> <P>DIAGNOSTIC APPROACH TO SOFT TISSUE TUMORS</P> <P>OVERVIEW</P> <P>BIOPSY AND RESECTION OF SOFT TISSUE TUMORS</P> <P>CLINICAL APPROACH</P> <P>AGE- AND LOCATION-BASED APPROACH TO DIAGNOSIS</P> <P>HISTOLOGIC APPROACH</P> <P>PATTERN-BASED APPROACH TO DIAGNOSIS</P> <P>FEATURE-BASED APPROACH TO DIAGNOSIS</P> <P>TUMORS OF ADIPOSE TISSUE</P> <P>BENIGN</P> <P>LIPOMA</P> <P>LIPOMATOSIS OF NERVE</P> <P>SYNOVIAL LIPOMATOSIS</P> <P>ANGIOLIPOMA</P> <P>SPINDLE CELL/PLEOMORPHIC LIPOMA</P> <P>CHONDROID LIPOMA</P> <P>MYOLIPOMA</P> <P>HIBERNOMA</P> <P>MYELOLIPOMA</P> <P>LIPOBLASTOMA</P> <P>INTERMEDIATE, LOCALLY AGGRESSIVE</P> <P>ATYPICAL LIPOMATOUS TUMOR/WELL-DIFFERENTIATED LIPOSARCOMA</P> <P>ATYPICAL SPINDLE CELL LIPOMATOUS TUMOR</P> <P>MALIGNANT</P> <P>DEDIFFERENTIATED LIPOSARCOMA</P> <P>MYXOID LIPOSARCOMA</P> <P>PLEOMORPHIC LIPOSARCOMA</P> <P>FIBROBLASTIC/MYOFIBROBLASTIC LESIONS</P> <P>BENIGN</P> <P>NODULAR FASCIITIS</P> <P>PROLIFERATIVE FASCIITIS/MYOSITIS</P> <P>ISCHEMIC FASCIITIS</P> <P>MYOSITIS OSSIFICANS</P> <P>FIBROOSSEOUS PSEUDOTUMOR OF THE DIGIT</P> <P>FIBROMA OF TENDON SHEATH</P> <P>DESMOPLASTIC FIBROBLASTOMA</P> <P>ELASTOFIBROMA</P> <P>ANGIOFIBROMA OF SOFT TISSUE</P> <P>MAMMARY-TYPE MYOFIBROBLASTOMA</P> <P>INTRANODAL PALISADED MYOFIBROBLASTOMA</P> <P>SUPERFICIAL CD34(+) FIBROBLASTIC TUMOR</P> <P>PLEOMORPHIC FIBROMA</P> <P>DERMATOMYOFIBROMA</P> <P>STORIFORM COLLAGENOMA</P> <P>KELOID</P> <P>NUCHAL-TYPE FIBROMA</P> <P>INTERMEDIATE (LOCALLY AGGRESSIVE)</P> <P>PALMAR/PLANTAR FIBROMATOSIS</P> <P>DESMOID-TYPE FIBROMATOSIS</P> <P>INTERMEDIATE (RARELY METASTASIZING)</P> <P>DERMATOFIBROSARCOMA PROTUBERANS</P> <P>SOLITARY FIBROUS TUMOR</P> <P>LOW-GRADE MYOFIBROBLASTIC SARCOMA</P> <P>INFLAMMATORY MYOFIBROBLASTIC TUMOR</P> <P>MYXOINFLAMMATORY FIBROBLASTIC SARCOMA</P> <P>MALIGNANT</P> <P>ADULT-TYPE FIBROSARCOMA</P> <P>MYXOFIBROSARCOMA</P> <P>LOW-GRADE FIBROMYXOID SARCOMA</P> <P>SCLEROSING EPITHELIOID FIBROSARCOMA</P> <P>PEDIATRIC FIBROBLASTIC/MYOFIBROBLASTIC TUMORS</P> <P>BENIGN</P> <P>FIBROUS HAMARTOMA OF INFANCY</P> <P>CALCIFYING APONEUROTIC FIBROMA</P> <P>CALCIFYING FIBROUS TUMOR</P> <P>INCLUSION BODY FIBROMATOSIS</P> <P>HYALINE FIBROMATOSIS SYNDROME</P> <P>FIBROMATOSIS COLLI</P> <P>GARDNER FIBROMA</P> <P>INTERMEDIATE (LOCALLY AGGRESSIVE)</P> <P>LIPOFIBROMATOSIS</P> <P>GIANT CELL FIBROBLASTOMA</P> <P>INTERMEDIATE (RARELY METASTASIZING)</P> <P>INFANTILE FIBROSARCOMA</P> <P>FIBROHISTIOCYTIC, HISTIOCYTIC, AND DENDRITIC CELL TUMORS</P> <P>BENIGN</P> <P>DERMATOFIBROMA AND FIBROUS HISTIOCYTOMA</P> <P>DEEP BENIGN FIBROUS HISTIOCYTOMA</P> <P>LOCALIZED-TYPE TENOSYNOVIAL GIANT CELL TUMOR</P> <P>DIFFUSE-TYPE TENOSYNOVIAL GIANT CELL TUMOR</P> <P>CELLULAR NEUROTHEKEOMA</P> <P>XANTHOMAS</P> <P>SOLITARY (JUVENILE) XANTHOGRANULOMA</P> <P>RETICULOHISTIOCYTOMA</P> <P>DEEP GRANULOMA ANNULARE</P> <P>RHEUMATOID NODULE</P> <P>LANGERHANS CELL HISTIOCYTOSIS</P> <P>EXTRANODAL ROSAI-DORFMAN DISEASE</P> <P>CRYSTAL-STORING HISTIOCYTOSIS</P> <P>INTERMEDIATE (RARELY METASTASIZING)</P> <P>PLEXIFORM FIBROHISTIOCYTIC TUMOR</P> <P>GIANT CELL TUMOR OF SOFT TISSUE</P> <P>MALIGNANT</P> <P>HISTIOCYTIC SARCOMA</P> <P>FOLLICULAR DENDRITIC CELL SARCOMA</P> <P>INTERDIGITATING DENDRITIC CELL SARCOMA</P> <P>SMOOTH MUSCLE TUMORS</P> <P>BENIGN</P> <P>SMOOTH MUSCLE HAMARTOMA</P> <P>SUPERFICIAL LEIOMYOMA</P> <P>DEEP LEIOMYOMA</P> <P>INTERMEDIATE</P> <P>EPSTEIN-BARR VIRUS-ASSOCIATED SMOOTH MUSCLE TUMOR</P> <P>MALIGNANT</P> <P>LEIOMYOSARCOMA</P> <P>PERICYTIC (PERIVASCULAR) TUMORS</P> <P>BENIGN</P> <P>GLOMUS TUMORS (AND VARIANTS)</P> <P>MYOPERICYTOMA</P> <P>MYOFIBROMA AND MYOFIBROMATOSIS</P> <P>ANGIOLEIOMYOMA</P> <P>TUMORS OF SKELETAL MUSCLE</P> <P>BENIGN</P> <P>FOCAL MYOSITIS</P> <P>ADULT RHABDOMYOMA</P> <P>FETAL RHABDOMYOMA</P> <P>GENITAL RHABDOMYOMA</P> <P>CARDIAC RHABDOMYOMA</P> <P>MALIGNANT</P> <P>EMBRYONAL RHABDOMYOSARCOMA</P> <P>ALVEOLAR RHABDOMYOSARCOMA</P> <P>SPINDLE CELL RHABDOMYOSARCOMA</P> <P>SCLEROSING RHABDOMYOSARCOMA</P> <P>PLEOMORPHIC RHABDOMYOSARCOMA</P> <P>EPITHELIOID RHABDOMYOSARCOMA</P> <P>VASCULAR TUMORS (INCLUDING LYMPHATICS)</P> <P>BENIGN</P> <P>PAPILLARY ENDOTHELIAL HYPERPLASIA</P> <P>BACILLARY ANGIOMATOSIS</P> <P>CONGENITAL HEMANGIOMA</P> <P>INFANTILE HEMANGIOMA</P> <P>LOBULAR CAPILLARY HEMANGIOMA</P> <P>EPITHELIOID HEMANGIOMA</P> <P>SPINDLE CELL HEMANGIOMA</P> <P>INTRAMUSCULAR HEMANGIOMA</P> <P>HOBNAIL HEMANGIOMA</P> <P>ACQUIRED TUFTED ANGIOMA</P> <P>MICROVENULAR HEMANGIOMA</P> <P>SINUSOIDAL HEMANGIOMA</P> <P>GLOMERULOID HEMANGIOMA</P> <P>ANGIOMATOSIS</P> <P>LYMPHANGIOMA</P> <P>MASSIVE LOCALIZED LYMPHEDEMA</P> <P>INTERMEDIATE (LOCALLY AGGRESSIVE)</P> <P>KAPOSIFORM HEMANGIOENDOTHELIOMA</P> <P>INTERMEDIATE (RARELY METASTASIZING)</P> <P>PAPILLARY INTRALYMPHATIC ANGIOENDOTHELIOMA</P> <P>RETIFORM HEMANGIOENDOTHELIOMA</P> <P>COMPOSITE HEMANGIOENDOTHELIOMA</P> <P>PSEUDOMYOGENIC HEMANGIOENDOTHELIOMA</P> <P>ATYPICAL VASCULAR LESION</P> <P>MALIGNANT</P> <P>EPITHELIOID HEMANGIOENDOTHELIOMA</P> <P>ANGIOSARCOMA</P> <P>KAPOSI SARCOMA</P> <P>CHONDRO-OSSEOUS TUMORS</P> <P>BENIGN</P> <P>SOFT TISSUE CHONDROMA</P> <P>SYNOVIAL CHONDROMATOSIS</P> <P>MALIGNANT</P> <P>EXTRASKELETAL OSTEOSARCOMA</P> <P>EXTRASKELETAL MESENCHYMAL CHONDROSARCOMA</P> <P>PERIPHERAL NERVE SHEATH TUMORS</P> <P>BENIGN</P> <P>SOLITARY CIRCUMSCRIBED NEUROMA</P> <P>SCHWANNOMA</P> <P>NEUROFIBROMA</P> <P>PERINEURIOMA</P> <P>HYBRID NERVE SHEATH TUMOR</P> <P>GRANULAR CELL TUMOR</P> <P>DERMAL NERVE SHEATH MYXOMA</P> <P>GANGLIONEUROMA</P> <P>NEUROMUSCULAR CHORISTOMA</P> <P>INTERMEDIATE</P> <P>MELANOTIC SCHWANNOMA</P> <P>MALIGNANT</P> <P>MALIGNANT PERIPHERAL NERVE SHEATH TUMOR</P> <P>EPITHELIOID MALIGNANT PERIPHERAL NERVE SHEATH TUMOR</P> <P>ECTOMESENCHYMOMA</P> <P>GENITAL STROMAL TUMORS</P> <P>FIBROEPITHELIAL STROMAL POLYP</P> <P>ANGIOMYOFIBROBLASTOMA</P> <P>CELLULAR ANGIOFIBROMA</P> <P>DEEP (AGGRESSIVE) ANGIOMYXOMA</P> <P>TUMORS OF MESOTHELIAL CELLS</P> <P>BENIGN</P> <P>ADENOMATOID TUMOR</P> <P>MULTICYSTIC PERITONEAL MESOTHELIOMA</P> <P>WELL-DIFFERENTIATED PAPILLARY MESOTHELIOMA</P> <P>MALIGNANT</P> <P>MALIGNANT MESOTHELIOMA</P> <P>HEMATOPOIETIC TUMORS IN SOFT TISSUE</P> <P>SOLITARY EXTRAMEDULLARY PLASMACYTOMA</P> <P>MYELOID SARCOMA</P> <P>LYMPHOMA OF SOFT TISSUE</P> <P>TUMORS OF UNCERTAIN DIFFERENTIATION</P> <P>BENIGN</P> <P>INTRAMUSCULAR MYXOMA</P> <P>JUXTAARTICULAR MYXOMA</P> <P>SUPERFICIAL ANGIOMYXOMA</P> <P>ACRAL FIBROMYXOMA</P> <P>PLEOMORPHIC HYALINIZING ANGIECTATIC TUMOR</P> <P>ANEURYSMAL BONE CYST OF SOFT TISSUE</P> <P>ECTOPIC HAMARTOMATOUS THYMOMA</P> <P>INTERMEDIATE (LOCALLY AGGRESSIVE)</P> <P>HEMOSIDEROTIC FIBROLIPOMATOUS TUMOR</P> <P>INTERMEDIATE (RARELY METASTASIZING)</P> <P>ATYPICAL FIBROXANTHOMA</P> <P>ANGIOMATOID FIBROUS HISTIOCYTOMA</P> <P>OSSIFYING FIBROMYXOID TUMOR</P> <P>MYOEPITHELIOMA OF SOFT TISSUE</P> <P>PHOSPHATURIC MESENCHYMAL TUMOR</P> <P>MALIGNANT</P> <P>SYNOVIAL SARCOMA</P> <P>EPITHELIOID SARCOMA</P> <P>ALVEOLAR SOFT PART SARCOMA</P> <P>CLEAR CELL SARCOMA</P> <P>PERIVASCULAR EPITHELIOID CELL TUMOR (PECOMA)</P> <P>DESMOPLASTIC SMALL ROUND CELL TUMOR</P> <P>EXTRASKELETAL EWING SARCOMA</P> <P>EXTRASKELETAL MYXOID CHONDROSARCOMA</P> <P>EXTRARENAL RHABDOID TUMOR</P> <P>INTIMAL SARCOMA</P> <P>UNDIFFERENTIATED/UNCLASSIFIED SARCOMAS</P> <P>UNDIFFERENTIATED PLEOMORPHIC SARCOMA</P> <P>UNDIFFERENTIATED ROUND CELL SARCOMA WITH *CIC-DUX4* TRANSLOCATION</P> <P>BCOR-CCNB3 (EWING-LIKE) SARCOMA</P> <P>MESENCHYMAL TUMORS OF THE GASTROINTESTINAL TRACT</P> <P>BENIGN NEURAL GASTROINTESTINAL POLYPS</P> <P>GASTROINTESTINAL STROMAL TUMOR</P> <P>GASTROINTESTINAL SCHWANNOMA</P> <P>GASTROINTESTINAL SMOOTH MUSCLE NEOPLASMS</P> <P>INFLAMMATORY FIBROID POLYP</P> <P>GANGLIOCYTIC PARAGANGLIOMA</P> <P>PLEXIFORM FIBROMYXOMA</P> <P>MALIGNANT GASTROINTESTINAL NEUROECTODERMAL TUMOR</P> <P>OTHER ENTITIES</P> <P>BENIGN</P> <P>AMYLOIDOMA</P> <P>GANGLION CYST</P> <P>TUMORAL CALCINOSIS</P> <P>IDIOPATHIC TUMEFACTIVE FIBROINFLAMMATORY LESIONS</P> <P>CARDIAC MYXOMA</P> <P>CARDIAC FIBROMA</P> <P>CONGENITAL GRANULAR CELL EPULIS</P> <P>NASOPHARYNGEAL ANGIOFIBROMA</P> <P>SINONASAL GLOMANGIOPERICYTOMA</P> <P>ECTOPIC MENINGIOMA</P> <P>GLIAL HETEROTOPIA</P> <P>INTERMEDIATE</P> <P>PARAGANGLIOMA</P> <P>PERIPHERAL HEMANGIOBLASTOMA</P> <P>MELANOTIC NEUROECTODERMAL TUMOR OF INFANCY</P> <P>EPENDYMOMA OF SOFT TISSUE</P> <P>MALIGNANT</P> <P>METASTATIC TUMORS TO SOFT TISSUE SITES</P> <P>NEUROBLASTOMA AND GANGLIONEUROBLASTOMA</P> <P>EXTRAAXIAL SOFT TISSUE CHORDOMA</P> <P>UNDIFFERENTIATED EMBRYONAL SARCOMA OF THE LIVER</P> <P>PRIMARY PULMONARY MYXOID SARCOMA</P> <P>BIPHENOTYPIC SINONASAL SARCOMA</P> <P>SPINDLE EPITHELIAL TUMOR WITH THYMUS-LIKE DIFFERENTIATION</P> <P>LOW-GRADE ENDOMETRIAL STROMAL SARCOMA</P>

ANATOMIA PATOLOGICA
ONCOLOGIA
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