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1: Renal Tumors and Tumor-Like Conditions; 1.1 Basic Anatomy and Histology; 1.2 Overview; 1.3 Familial Renal Cancer; 1.3.1 Von Hippel-Lindau (VHL) Clear Cell Renal Cell Carcinoma (RCC); 1.3.2 Hereditary Papillary RCC; 1.3.3 Hereditary Leiomyomatosis RCC; 1.3.4 Birt-Hogg-Dube Syndrome; 1.4 Renal Cell Carcinoma; 1.4.1 Clear Cell RCC; 1.4.2 Multilocular Cystic Clear Cell Renal Cell Neoplasm of Low Malignant Potential; 1.4.3 Papillary RCC; 1.4.4 Chromophobe RCC; 1.4.5 Hybrid Oncocytic Chromophobe Tumor (HOCT); 1.4.6 Collecting Duct Carcinoma; 1.4.7 Renal Medullary Carcinoma
1.4.8 Mucinous, Tubular and Spindle Cell Carcinoma1.4.9 Renal Cell Carcinoma After Neuroblastoma; 1.4.10 RCC with Sarcomatoid or Rhabdoid Differentiation; 1.4.11 Renal Cell Carcinoma, Unclassified; 1.5 Proposed New and Emerging Epithelial Renal Tumors; 1.5.1 Tubulocystic Renal Cell Carcinoma; 1.5.2 Acquired Cystic Disease-Associated RCC; 1.5.3 Clear Cell Papillary (Tubulo-Papillary) RCC; 1.5.4 MiT Family Translocation RCC; 1.5.5 Thyroid-Like Follicular Renal Cell Carcinoma; 1.5.6 Succinic Dehydrogenase B Deficiency Associated Renal Cell Carcinoma; 1.5.7 ALK-Translocation Renal Cell Carcinoma
1.5.8 Renal Cell Carcinoma with Smooth Muscle Stroma1.5.9 Tuberous Sclerosis-Associated Renal Cell Carcinoma; 1.6 Benign Tumors; 1.6.1 Papillary Adenoma; 1.6.2 Metanephric Tumors; 1.6.3 Renal Oncocytoma; 1.7 Percutaneous Biopsy of Renal Tumours; 1.8 Cystic Nephroma and Mixed Epithelial and Stromal Tumors; 1.9 Soft Tissue Tumors; 1.9.1 Medullary Fibroma; 1.9.2 Juxtaglomerular Cell Tumor; 1.9.3 Glomus Tumor; 1.9.4 Angiomyolipoma; 1.9.5 Epithelioid Angiomyolipoma; 1.9.6 Leiomyoma; 1.9.7 Lipoma; 1.9.8 Hemangioma; 1.9.9 Lymphangioma; 1.9.10 Schwannoma; 1.9.11 Solitary Fibrous Tumor
1.9.12 Leiomyosarcoma1.9.13 Angiosarcoma; 1.9.14 Liposarcoma; 1.9.15 Rhabdomyosarcoma; 1.9.16 Malignant Fibrous Histiocytoma; 1.9.17 Hemangiopericytoma; 1.9.18 Hemangioblastoma; 1.9.19 Osteosarcoma; 1.9.20 Other Soft Tissue Tumors; 1.10 Wilms' Tumor and Other Renal Neoplasms in Children; 1.10.1 Nephrogenic Rests and Nephroblastomatosis; 1.10.2 Nephroblastoma (Wilms' Tumor); 1.10.3 Cystic Partially Differentiated Nephroblastoma; 1.10.4 Congenital Mesoblastic Nephroma (CMN); 1.10.5 Clear Cell Sarcoma of Kidney; 1.10.6 Rhabdoid Tumor of Kidney; 1.10.7 Neuroblastoma
1.10.8 Primitive Neuroectodermal Tumor (PNET)1.10.9 Desmoplastic Small Round Cell Tumor; 1.10.10 Synovial Sarcoma; 1.10.11 Ossifying Renal Tumor of Infancy; 1.11 Other Rare Tumors and Tumor-Like Conditions; 1.11.1 Neuroendocrine Tumors; 1.11.2 Hematopoietic and Lymphoid Tumors; 1.11.3 Germ Cell Tumors; 1.11.4 Other Rare Epithelial Tumors and Renal Cell Carcinoma in Children; 1.11.5 Tumor-Like Conditions; 1.12 Secondary Tumors; Suggested Reading; 2: Tumors and Tumor-Like Conditions of Urinary Bladder, Renal Pelvis, Ureter and Urethra; 2.1 Introduction; 2.1.1 Basic Anatomy and Histology
1.4.8 Mucinous, Tubular and Spindle Cell Carcinoma1.4.9 Renal Cell Carcinoma After Neuroblastoma; 1.4.10 RCC with Sarcomatoid or Rhabdoid Differentiation; 1.4.11 Renal Cell Carcinoma, Unclassified; 1.5 Proposed New and Emerging Epithelial Renal Tumors; 1.5.1 Tubulocystic Renal Cell Carcinoma; 1.5.2 Acquired Cystic Disease-Associated RCC; 1.5.3 Clear Cell Papillary (Tubulo-Papillary) RCC; 1.5.4 MiT Family Translocation RCC; 1.5.5 Thyroid-Like Follicular Renal Cell Carcinoma; 1.5.6 Succinic Dehydrogenase B Deficiency Associated Renal Cell Carcinoma; 1.5.7 ALK-Translocation Renal Cell Carcinoma
1.5.8 Renal Cell Carcinoma with Smooth Muscle Stroma1.5.9 Tuberous Sclerosis-Associated Renal Cell Carcinoma; 1.6 Benign Tumors; 1.6.1 Papillary Adenoma; 1.6.2 Metanephric Tumors; 1.6.3 Renal Oncocytoma; 1.7 Percutaneous Biopsy of Renal Tumours; 1.8 Cystic Nephroma and Mixed Epithelial and Stromal Tumors; 1.9 Soft Tissue Tumors; 1.9.1 Medullary Fibroma; 1.9.2 Juxtaglomerular Cell Tumor; 1.9.3 Glomus Tumor; 1.9.4 Angiomyolipoma; 1.9.5 Epithelioid Angiomyolipoma; 1.9.6 Leiomyoma; 1.9.7 Lipoma; 1.9.8 Hemangioma; 1.9.9 Lymphangioma; 1.9.10 Schwannoma; 1.9.11 Solitary Fibrous Tumor
1.9.12 Leiomyosarcoma1.9.13 Angiosarcoma; 1.9.14 Liposarcoma; 1.9.15 Rhabdomyosarcoma; 1.9.16 Malignant Fibrous Histiocytoma; 1.9.17 Hemangiopericytoma; 1.9.18 Hemangioblastoma; 1.9.19 Osteosarcoma; 1.9.20 Other Soft Tissue Tumors; 1.10 Wilms' Tumor and Other Renal Neoplasms in Children; 1.10.1 Nephrogenic Rests and Nephroblastomatosis; 1.10.2 Nephroblastoma (Wilms' Tumor); 1.10.3 Cystic Partially Differentiated Nephroblastoma; 1.10.4 Congenital Mesoblastic Nephroma (CMN); 1.10.5 Clear Cell Sarcoma of Kidney; 1.10.6 Rhabdoid Tumor of Kidney; 1.10.7 Neuroblastoma
1.10.8 Primitive Neuroectodermal Tumor (PNET)1.10.9 Desmoplastic Small Round Cell Tumor; 1.10.10 Synovial Sarcoma; 1.10.11 Ossifying Renal Tumor of Infancy; 1.11 Other Rare Tumors and Tumor-Like Conditions; 1.11.1 Neuroendocrine Tumors; 1.11.2 Hematopoietic and Lymphoid Tumors; 1.11.3 Germ Cell Tumors; 1.11.4 Other Rare Epithelial Tumors and Renal Cell Carcinoma in Children; 1.11.5 Tumor-Like Conditions; 1.12 Secondary Tumors; Suggested Reading; 2: Tumors and Tumor-Like Conditions of Urinary Bladder, Renal Pelvis, Ureter and Urethra; 2.1 Introduction; 2.1.1 Basic Anatomy and Histology